Microbiota-dependent expansion of testicular IL-17-producing Vγ6+ γδ T cells upon puberty promotes local tissue immune surveillance

Abstract

γδT cells represent the majority of lymphocytes in several mucosal tissues where they contribute to tissue homoeostasis, microbial defence and wound repair. Here we characterise a population of interleukin (IL) 17-producing γδ (γδ17) T cells that seed the testis of naive C57BL/6 mice, expand at puberty and persist throughout adulthood. We show that this population is foetal-derived and displays a T-cell receptor (TCR) repertoire highly biased towards Vγ6-containing rearrangements. These γδ17 cells were the major source of IL-17 in the testis, whereas αβ T cells mostly provided interferon (IFN)-γ in situ. Importantly, testicular γδ17 cell homoeostasis was strongly dependent on the microbiota and Toll-like receptor (TLR4)/IL-1α/IL-23 signalling. We further found that γδ17 cells contributed to tissue surveillance in a model of experimental orchitis induced by intra-testicular inoculation of Listeria monocytogenes, as Tcrδ/− and Il17−/− infected mice displayed higher bacterial loads than wild-type (WT) controls and died 3 days after infection. Altogether, this study identified a previously unappreciated foetal-derived γδ17 cell subset that infiltrates the testis at steady state, expands upon puberty and plays a crucial role in local tissue immune surveillance.

Introduction

The male reproductive system is composed of a pair of testes, accessory glands, such as the seminal vesicles and the prostate and a series of ducts that serve to transport spermatozoa to the female reproductive tract. Whereas accessory glands secrete products of the seminal fluid that enable sperm viability and motility, the testis plays a central role as a unique environment where spermatogenesis occurs. This process is driven by Sertoli cells, integrated components of the seminiferous tubules that warrant an environment, in which germ cells can progress towards the mature stage of the spermatogenic cycle. On the other hand, Leydig cells secrete testosterone, which acts on the Sertoli and peritubular cells to ensure the stability of this environment as well as the formation of testicular interstitial fluid.1

For the past four decades, the testis has been regarded as an immune-privileged organ where germ cell antigens are protected from potential autoimmune responses.1 However, the notion of “immune privilege” needs to be revisited to acknowledge a physiological role for resident immune cell populations in the interstitial spaces of the testes. For example, it was shown that steady-state interactions between the immune system and meiotic germ cell antigens contribute to systemic tolerance.2 Moreover, secretion of anti-inflammatory cytokines by resident macrophages regulates the homoeostasis of the testicular immunosuppressive microenvironment.3 In addition, resident macrophages were reported to impact on steroidogenesis by regulating Leydig cell development and function.4 By highlighting a physiological role for immune cells present in male reproductive organs at steady state, these data provide important cues to our knowledge about male infertility.

Naturally, immune populations also provide a key line of defence in the testes against pathogenic bacteria, namely in response to Escherichia coli (E. coli), Chlamydia or Listeria monocytogenes (L. monocytogenes).5 Thus, we hypothesised the existence of critical immune mechanisms within the testis that would keep pathogens at bay and ensure reproduction.

γδ T cells only represent a minority among all lymphocytes in blood or secondary lymphoid tissues, but are highly enriched in mucosal tissues.6,7 There, they play crucial roles in mucosal immunity by acting as a first line of defence against several pathogens and tumours, in particular by local production of inflammatory cytokines such as interleukin (IL)-17 and interferon (IFN)-γ.7

The role of γδ T cells has been well characterised in the female reproductive tract, namely in the uterus, where they display a Vγ6-biased T-cell receptor (TCR) repertoire at steady state, and expand in the placenta and uterine decidua upon pregnancy.8 Interestingly, it has been proposed that seminal plasma can induce IL-17 production by uterine γδ T cells, promoting local inflammation important for embryo implantation.9 Furthermore, they provide protection against viral infection.10 In contrast, γδ T cells from male genitourinary organs remain poorly characterised. Whereas a Vγ6 population has been shown to be recruited during bacterial infection in the testis,11 and to impact on autoimmunity in a model of orchitis,12 the mechanisms controlling this response have not been described. Furthermore, while their presence has been associated with infertility disorders in humans,13 a potential impact of γδ T cells on steady-state testicular physiology remains to be elucidated.

By combining microscopy and flow-cytometry analyses, and employing a series of genetically modified specific pathogen-free (SPF), as well as germ-free (GF) mice, this study provides a comprehensive characterisation of γδ T cells in the testis at steady state and during inflammation. We demonstrate that γδ T cells are highly biased towards a foetal-derived TCR repertoire dominated by gamma-chain variable region (Vγ) 6 and strongly expand in the interstitial space of healthy testis during puberty. Furthermore, we show that testicular γδ T cells account for almost all local IL-17 producers at steady state, and that their homoeostasis relies on the symbiotic microbiome and on the Toll-like receptor (TLR)4/IL-1α/IL-23 signalling axis. While they seemingly do not impact on steady-state spermatogenesis and testosterone production, we document an important role of γδ17 cells in testicular immune surveillance upon L. monocytogenes infection. As bacterial infections and associated inflammation within male reproductive organs can lead to orchitis and associated reproductive disorders,14 we believe that our study provides cues on protective immune mechanisms that may be exploited for new immune-mediated strategies against male infertility.

Results

Testicular γδ T cells display a typical phenotype biased for IL-17 production

To characterise γδ T cells from the male reproductive tract, we analysed their distribution and phenotype in naive C57BL/6 mice by flow cytometry. We found that γδ T cells represented 50% of total CD3+ T cells in testis (Fig. 1a), while they were less frequent in prostate and seminal vesicle (SV) (Supplementary Fig. S1A). Testicular γδ T cells displayed a homogeneous activated CD69+CD44hiCD62Llow profile of tissue-resident effector T cells, while conventional αβ T cells were less activated in the testis (Fig. 1b). Importantly, the γδ TCR repertoire was mostly restricted to the usage Vγ6 (Fig. 1c). This was in sharp contrast to γδ T cells from the SV and prostate that comprised diverse Vγ subsets, and of which only 20% were activated CD44hi cells (Supplementary Fig. S1B, C). The Vγ6 chain usually pairs with Vδ1 to form an invariant TCR in distinct foetal thymus-derived γδ T cells reported to colonise various non-lymphoid tissue in the perinatal period of life.15 To further confirm that embryonic thymus-derived Vγ6+ γδ T cells populate the testis, we analysed Indu-Rag1×TcrdH2BeGFP mice. Treating these mice with tamoxifen induces the expression of the Rag1 enzyme and thereby the maturation of B and T cells in adult organisms including γδ T cells. In addition, in Indu-Rag1×TcrdH2BeGFP mice, induced γδ T cells express histone-bound eGFP. Indu-Rag1×TcrdH2BeGFP mice not treated with tamoxifen lack γδ T cells.16 Hence, consistent with their embryonic origin and contrary to their αβ T-cell counterparts, Vγ6+ γδ T cells could not be reconstituted in the testis of Indu-Rag1×TcrdH2BeGFP mice after tamoxifen-mediated induction of Rag1 expression (Fig. 1d). In line with their Vγ6+ phenotype, testicular γδ T cells exhibited a typical signature of bona fide IL-17 producers,17 namely expressing the master transcription factor RORγt (Fig. 1e) while lacking CD27 (Fig. 1f). In contrast, αβ T cells expressed neither RORγt nor T-bet, but CD27, emphasising their naive phenotype within the testis (Fig. 1e, f). Importantly, the majority of testicular γδ T cells expressed IL-17, but not IFN-γ, after ex vivo stimulation with PMA and ionomycin (Fig. 1g), whereas γδ T cells from reproductive accessory glands produced equally IFN-γ and IL-17 (Supplementary Fig. S1D). Most importantly, we confirmed the testicular γδ T-cell phenotype using an IL-17-GFP/IL-22-BFP reporter mouse model18 (Fig. 1h), which allowed the detection of IL-17 producers in steady state while bypassing the need for PMA/ionomycin restimulation. Of note, the expression of IL-22 could neither be detected in the reporter mice (Fig. 1h) nor with a classical intracellular staining after PMA/ionomycin restimulation (data not shown).

Fig. 1: Testicular γδ T cells display a typical phenotype biased for IL-17 production.
figure1

a Representative contour plots depicting γδ (middle) and CD4 and CD8 αβ (right) T cells gated on CD3+CD45+ cells (left) in testes of C57BL/6 mice (8–12 weeks old). Scatter plot shows frequencies and absolute numbers of γδ, CD4 and CD8 T cells among CD45+CD3+ cells (n = 5–16, two to five independent experiments). b Representative histogram of CD69, CD44 and CD62L expression of γδ (dark grey) and αβ (white) T cells. Scatter plot displays frequencies of indicated cell populations among γδ (black) and αβ (white) T cells (n = 8–17, two to five independent experiments). c Representative contour plot and pie chart depicting mean frequencies of Vγ1 + , Vγ4+, Vγ5+ and Vγ6+ γδ T cells in testes (n = 6–12, three independent experiments). d Scatter plot shows frequencies of αβ and γδ T cells in testes of WT (black) and Indu-Rag1×TcrdH2BeGFP (white) mice (n = 5–9, three independent experiments). e Representative contour plot and scatter plot of RORγt and T-bet expression in testicular γδ (left, black) and αβ (right, white) T cells (n = 5, one independent experiment). f Representative histogram of CD27 expression on γδ (grey) and αβ (white) T cells. Scatter plot with frequencies of CD27+ cells among γδ (black) and αβ (white) T cells (n = 6, two independent experiments). g Representative contour plot and scatter plot of IL-17 versus IFN-γ expression in testicular γδ (left, black) and αβ (right, white) T cells (n = 20–21, five independent experiments) after ex vivo stimulation of testicular lymphocytes with PMA and ionomycin. h Representative contour plot and scatter plot of IL-17 versus IL-22 expression in IL-17GFP/IL-22-BFP reporter mice, without prior stimulation by PMA and ionomycin (n = 3–6). i Pie chart depicting indicated immune cell subsets contributing to IL-17 (left) or IFN-γ (right) production in the testis after ex vivo stimulation by PMA and ionomycin (n = 12, three independent experiments). Data are represented as mean ± SD.

We also assessed the contribution of γδ T cells to the entire cytokine production of ex vivo-stimulated lymphocytes from testes and accessory glands. In all cases, we observed a clear discrimination of function, since γδ T cells were the main producers of IL-17, whereas IFN-γ was mostly expressed by αβ T cells (Fig. 1i). Given their recently described impact on organ physiology,19,20,21 we decided to further focus on studying the homoeostasis and potential functions of Vγ6+ γδ17 infiltrating the testis.

Vγ6+ IL-17+ γδ T cells accumulate specifically in the testis upon puberty

To investigate whether changes associated with physiological maturation of the reproductive tract could impact on γδ T-cell homoeostasis in the testis, we next characterised this population before and after puberty. We analysed testes of pre- (3–5-week-old) and post-pubertal (7–12-week-old) mice, as recommended by Jackson Laboratories.

Our data show that γδ T cells colonise the testis before puberty, as depicted by the small but sizeable population of testicular γδ T cells observed in 3–5-week-old mice, but expand drastically during puberty (Fig. 2a, b). The observed 12-fold increase in cell numbers was mainly due to the Vγ6+ subset (Fig. 2c, d) and IL-17-producing γδ T cells (Fig. 2e, f). While γδ T-cell infiltration of the testes may be partially driven by CCR6 (Fig. 2g), as previously reported,22 our data also suggested that the maturing testicular microenvironment specifically triggers the proliferation of Vγ6+ T cells during the onset of puberty, as this subset exhibited enhanced proliferative marks when stained for Ki67 (Fig. 2h).

Fig. 2: Vγ6+ IL-17+ γδ T cells accumulate specifically in the testis during puberty.
figure2

a Representative contour plots depicting testicular γδ and αβ T cells gated on CD3+CD45+ cells before puberty (3–5-week-old (wo) mice) and post puberty (7–12-week-old mice). Scatter plot shows frequencies of γδ T cells among CD3+CD45+ cells in pre-pubertal (white) and post-pubertal (black) mice (n = 32–36, seven independent experiments). b Number (#) of γδ T cells in pre- (white) and post-pubertal (black) mice (n = 22–27, five independent experiments). c Representative contour plots depicting Vγ6+ γδ T cells before and after puberty. Scatter plot shows frequencies of Vγ6+ γδ T cells among lymphocytes in pre-pubertal (white) and post-pubertal (black) mice (n = 14–19, three independent experiments). d Number of Vγ6+ γδ T cells in pre- (white) and post-pubertal (black) mice (n = 14, three independent experiments). e Representative contour plots depicting IL-17-producing γδ T (γδ17) cells before and after puberty. Scatter plot shows frequencies of γδ17 cells in pre-pubertal (white) and post-pubertal (black) mice (n = 8–9, two independent experiments). f Number of γδ17 cells in pre- (white) and post-pubertal (black) mice (n = 8, two independent experiments). g Representative histogram of CCR6 expression of γδ in pre- (white) and post-pubertal (dark grey) mice. Scatter plot shows frequencies of CCR6+ γδ in pre-pubertal (white) and post-pubertal (black) mice (n = 8–9, two independent experiments). h Representative histogram of Ki67 expression of Vγ6+ γδ T cells in pre- (white) and post-pubertal (dark grey) mice (n = 7–9, three independent experiments). Data are represented as mean ± SD as evaluated by unpaired Student’s t test, **P < 0.01, ***P < 0.001, ****P < 0.0001.

Microbiota, TLR4 and IL-23 signalling drives the accumulation of γδ17 cells in the testis

We next investigated the molecular cues underlying the accumulation of testicular γδ T cells upon puberty. The maturation of the reproductive tract generally associates with important environmental changes, including a boost of steroidogenesis23 and a bidirectional crosstalk between the male endocrine system and the symbiotic microbiome established during puberty.24,25 Given that the microbiota can promote the differentiation of IL-17-producing CD4+ cells in the gut26 and can control the migration and homoeostasis of γδ17 cells to different tissues,27,28,29 we hypothesise that commensal bacteria could also influence testicular γδ17 cell accumulation at puberty. Thus, we compared the immune populations within the testis from adult mice hosted in GF versus SPF conditions. Adult GF mice exhibited a significant reduction in γδ T-cell frequencies and absolute numbers (Fig. 3a, b). Among total testicular γδ T cells, the IL-17-producing Vγ6+ subset was selectively affected in GF compared with SPF mice (Fig. 3c, d). By contrast, the production of testicular IFN-γ was not altered by the absence of symbiotic bacteria (Supplementary Fig. S2). Importantly, an increase in IL-17-producing Vγ6+ γδ T cells as observed in SPF mice post puberty did not similarly occur in GF mice, confirming a microbiota-dependent expansion of testicular γδ17 cells at puberty (Fig. 3d).

Fig. 3: Accumulation of γδ T cells in the testis is dependent on microbiota, IL-23 and TLR4 signalling.
figure3

a Representative contour plots depicting IL-17-producing γδ T cells gated on CD3+CD45+ cells in testes of specific pathogen-free (SPF) (left) and germ-free (GF) (right) mice. Scatter plot shows frequencies of γδ and γδ17 T cells among lymphocytes in testes of SPF (black) and GF (white) mice (n = 18–22, five independent experiments). b Number of testicular γδ and γδ17 cells of SPF (black) and GF (white) mice (n = 11–12, three independent experiments). c Representative contour plots depicting testicular Vγ6+ γδ T cells gated on CD3+CD45+ cells of SPF and GF mice. Scatter plot displays frequencies of Vγ6+ γδ T cells among all T cells in testes of SPF (black) and GF (white) mice (n = 11–14, four independent experiments). d Number of Vγ6+ γδ T cells from SPF and GF in pre- and post-pubertal mice (n = 6, two independent experiments) (n = 7–8, three independent experiments). e Scatter plot shows frequencies of γδ17 T cells among lymphocytes of WT (black), Tlr2−/−, Tlr4−/− and Myd88−/− (white) mice (n = 4–9, one to two independent experiments). f Representative histogram of γδ (dark grey) and αβ (white) T cells expressing IL-1 receptor (R) in WT mice (left) and IL-23R in Il23rgfp/gfp mice (right) and scatter plot with mean fluorescence intensity (MFI) (n = 5–10, one to three independent experiments). g Scatter plot depicts frequencies of γδ17 among all T cells in testes of WT (black), Il1r−/−, Il23r−/−, Il1α−/− and Il1β/− (white) (n = 5–29, one to three independent experiments). h Scatter plot displays picogram (pg) per mg protein of IL-1α, IL-1β and IL-23 in the testis (n = 9, two independent experiments). Data are represented as mean ± SD as evaluated by Kruskal–Wallis test followed by Dunn’s multiple-comparison test or one-way ANOVA followed by Holm–Sidak’s multiple-comparison test. **P < 0.01, ***P < 0.001, ****P < 0.0001.

Commensal microbiota and their metabolites can act as pathogen-associated molecule patterns (PAMPs) to trigger TLR- signalling.30 Importantly, TLR4- and TLR2-stimulated myeloid cells promote γδ17 cell proliferation in an inflammatory set-up through the production of IL-1β and IL-23.31,32 Therefore, we asked whether γδ17 cell frequencies in the testis were influenced by TLR signalling and downstream cytokines, and analysed mice deficient for these candidates. Interestingly, we observed that steady-state γδ17 cell homoeostasis in the testes mainly relied on TLR4- but not TLR2 signals, as this subset was significantly reduced in mice deficient (/−) for TLR4, whereas it was not significantly affected in Tlr2/− mice (Fig. 3e). Of note, TLR4 in the testis was mainly expressed by dendritic cells (Supplementary Fig. S3A). Consistently, the percentage of γδ17 cells was also decreased in Myd88−/− mice, a key adaptor protein downstream of most TLR-signalling pathways (Fig. 3e).

We next anticipated that TLR4 triggering would promote the production of IL-1 and IL-23, which would in turn be responsible for γδ17 cell accumulation in the testis. In line with this, we observed that testicular γδ T cells constitutively expressed the receptors for IL-1 and IL-23, in sharp contrast with their αβ counterpart (Fig. 3f). Importantly, Il1r−/− or Il23r−/− mice recapitulated the reduction of γδ17 cell percentages observed in Tlr4−/− animals, pointing at a crucial and non-redundant function of these cytokines for steady-state testicular γδ T-cell homoeostasis (Fig. 3g). Interestingly, IL-1α rather than IL-1β was seemingly required in this process (Fig. 3g, h). Altogether, these data indicate that testicular γδ17 cells are regulated by IL-1α/IL-23 and the TLR4/MyD88 signalling pathways potentially triggered by symbiotic microbial cues.

γδ T cells do not influence steady-state testicular physiology

In order to anticipate any potential role(s) for γδ T cells on testis steady-state physiology, we next investigated their localisation by microscopy by using γδ T-cell reporter mice (TcrdH2BeGFP). γδ T cells in TcrdH2BeGFP mice express a histone-bound eGFP; accordingly the expression of γδ T-cell-specific eGFP is very stable and located in the nucleus of γδ T cells. Ex vivo two-photon laser- scanning microscopy of testes extracted from adult TcrdH2BeGFP reporter mice and immobilised in an oxygen-flushed chamber revealed that most γδ T cells in the testis were motile (Fig. 4a; Supplementary Movie S1). Next, immunofluorescence microscopy of testis organ slices from TcrdH2BeGFP mice confirmed that γδ T cells were mainly found in the interstitial stromal compartment that surrounds seminiferous tubules (Fig. 4b). Thus, γδ T cells are in proximity to Leydig and Sertoli cells, which are responsible for testosterone production and spermatogenesis, respectively. Notably, both of these specialised testicular cell types are seemingly equipped to respond to IL-17 as shown by their receptor expression (Supplementary Fig. S3B). We therefore search for a potential impact of γδ17 cells on the biological functions of Leydig and Sertoli cells.

Fig. 4: γδ T cells do not impact on testicular steady-state physiology.
figure4

a Two-photon microscopy of the testis of adult TcrdH2BeGFP mice demonstrating γδ T cells (green) and collagen structures (white–grey). Using IMARIS software, motile γδ T cells were tracked (cyan lines). Scale bar represents 70 μM (n = 6 movies). b Representative immunofluorescence staining of cross sections from the testis of adult TcrdH2BeGFP mice against CD3 (red) and DAPI (white) for nuclear visualisation. Scale bars represent 50 μM (n = 4). c Representative histogram of germ cells in a WT mouse. Plot shows frequencies of germ cells of WT, Tcrδ−/− and Il17−/− mice (n = 3–5, one to two independent experiments). d Representative microphotographs of the testis of WT and Il17/− mice. Organs are alike in aspect, proportion and volume, with similar contribution of seminiferous tubules (white arrowhead), Leydig cells in the stromal compartment (black arrowhead) and with numerous spermatozoa in the lumen of the epididymis (asterisk). Haematoxylin and eosin staining. Original magnification ×1.25 (top column, bar, 2 mm) and ×20 (middle and lower columns, bar, 100 µm) (n = 3). e Scatter plot displays ng of testosterone/mg of protein in Tcrδ/− and Il17−/ mice compared with the respective littermate controls (n = 16–25, four independent experiments). Data represented as mean ± SD.

We first dissected the spermatogenesis process from WT, Tcrδ/– and Il17−/− mice by flow cytometry, identifying the different germ cell stages according to their DNA content. No differences were found between Tcrδ/− and Il17−/− mice and WT controls, indicating that testicular IL-17 does not impact on germ cell differentiation (Fig. 4c). Furthermore, Tcrδ−/− and Il17/ mice did not show particular abnormalities of their overall testis morphology and histological structures (Fig. 4d). Finally, testosterone levels in the serum of Il17/− and Tcrδ/ mice were similar to their respective littermate controls (Fig. 4e). Altogether, these data support the absence of γδ T-cell overall impact on steady-state testis physiology, and go in line with a normal fertility displayed by our Tcrδ−/− and Il17–/− colonies.

Testicular γδ17 cells promote immune surveillance against Listeria monocytogenes

Finally, as γδ T cells are well known to mediate immune surveillance in mucosal tissues as well as in the skin,7 we hypothesised that surveillance mechanism might be also important during testis infection. This concept has previously been suggested by studies, where depletion of γδ T cells exacerbated testicular inflammation upon bacterial infection.12,33 However, molecular mechanisms and pathophysiological outcomes have not been elucidated.

Here we performed intra-testicular bacterial infection with Listeria monocytogenes (L. monocytogenes) as a model of experimental orchitis.12 We found that both γδ and αβ T cells accumulated in the infected testis (Fig. 5a)—but not in the spleen (Fig. 5b)—and mainly expressed IFN-γ (Fig. 5c, d). While the γδ17 cell Vγ-chain repertoire was mostly conserved upon infection compared with steady state, we observed that the IFN-γ+ population rather displayed a diverse repertoire composed of Vγ1+, Vγ4+ and Vγ1Vγ4 cells (Fig. 5d). Interestingly, the accumulation of testicular IFN-γ-producing γδ T cells after infection with L. monocytogenes was reduced in Il17/− mice compared with their WT littermate controls. Similarly, we observed a reduction of IFN-γ- producing CD8+ and CD4+ T cells in infected testes in Il17−/− as well as Tcrδ–/− mice, suggesting a role for γδ T cells and IL-17 in the amplification of the type 1 response in this model (Fig. 5e). This presence of IFN-γ producers was necessary to resolve intra-testicular bacterial infection, as all Ifnγ−/− animals died within 3 days in response to a low (2 × 103 CFUs) dose of L. monocytogenes, whereas 60% of Il17/−, 80% of Tcrδ−/− and 100% of WT mice were still alive at 8 days after infection (Fig. 5f).

Fig. 5: Testicular γδ17 promotes testis surveillance against Listeria monocytogenes.
figure5

a, b Scatter plots show frequencies and numbers of γδ and αβ T cells among CD3+CD45+ cells after intra-testicular infection with L. monocytogenes (L. mon) (2 × 103 CFU) (white) or PBS (black) in mature testis (n = 10–13, three independent experiments) (a) and spleen (n = 5–8, two independent experiments) (b). c Representative contour plots depicting IL-17+ or IFN-γ+ γδ (left) and αβ (right) T cells 3 days after intra-testicular injection of PBS (top) or L. monocytogenes (bottom). Scatter plots show frequencies of IFN-γ+ (white) and IL-17+ (black) γδ (top) and αβ (bottom) T cells (n = 10–13, three independent experiments). d Pie charts displaying the Vγ1+, Vγ4+ and Vγ1Vγ4 usage of IL-17+ γδ (top) and IFN-γ+ (bottom) γδ T cells 3 days after intra-testicular injection of L. mon (n = 8, two independent experiments). e Scatter plots show numbers of IFN-γ+ CD4 (left), CD8 (middle) and γδ (right) T cells in mature testis of WT (black), Tcrδ/− (grey) and Il17−/− (white) mice after intra-testicular infection with L. monocytogenes (2 × 103 CFU) or PBS (n = 8–19, three independent experiments). f Survival curve of WT (white), Ifnγ−/− (red), Il17−/ (white) and Tcrδ/− (grey) mice after intra-testicular injection of L. monocytogenes (2 × 103 CFU) (n = 6–7, three independent experiments). g Bacterial burden (CFU per testis) of WT (black), Tcrδ/− (grey) and Il17/− (white) mice analysed 72 h after intra-testicular injection of L. mon (2 × 103 CFU) (n = 11–12, three independent experiments). h Survival curve of WT (white), Il17−/− (black) and Tcrδ/− (grey) mice after intra-testicular injection of L. monocytogenes (4 × 103 CFU) (n = 5–7). Data pooled are represented as mean ± SD as evaluated by Kruskal–Wallis test followed by Dunn’s multiple-comparison test or one-way ANOVA followed by Holm–Sidak’s multiple-comparison test. *P < 0.05, **P < 0.01. i Bacterial burden (CFU per testis) of WT (black), Tcrδ–/– (grey) and Il17−/− (white) mice analysed 48 h after intra-testicular injection of L. monocytogenes (4 × 103 CFU) (n = 3–5 animals/group). When possible, Tcrδ+/+ and Il17+/+ littermate controls were used and referred as WT animals.

This notwithstanding, testicular IL-17+ cells were required to control bacterial burden, as Il17/− displayed higher L. monocytogenes loads compared with their WT littermate controls 3 days post infection (Fig. 5g). Importantly, this translated into a poor survival outcome in response to a high (4 × 103 CFUs) dose of L. monocytogenes, as all Il17−/− and Tcrδ−/− animals died within 3 days of infection, whereas 80% of the WT control mice were still alive after 8 days of infection (Fig. 5h). Interestingly, despite the higher susceptibility of Il17/− and Tcrδ−/− animals after low- and high-dose infection, a compensatory expansion of other IL-17-producing lymphocytes, such as NKT and MAIT cells,34 (C. Paget, Personal communication) might have contributed to a lower bacterial burden in Tcrδ−/− animals (Fig. 5i).

Altogether, our data highlight a crucial role for testicular γδ17 cells as a first line of defence against bacterial infection.

Discussion

Over the past few years, tissue-resident γδ T cells have been explored in many specific tissues, such as the skin,35 lung,36 gingiva,29 eye,37 trachea38 and brain meninges,21 and also in the female sexual organs such as the uterus and vagina.8,10,39 Therefore, it is not surprising that γδ T cells are also present in the male reproductive organs. Unexpectedly, γδ T cells accounted for almost 50% of all lymphocytes in “immune privileged” testis. These testicular γδ T cells constituted a rather uniform population as almost all cells showed a terminally differentiated CD69+CD44hiCD62Llow phenotype, and their TCR repertoire was highly biased for Vγ6-containing rearrangements, which are known to take place during foetal life.16 This γδ T-cell phenotype appears to be unique to the testis, as other sex organs of the male reproductive tract, like the accessory glands, exhibit a diverse and heterogeneous population of γδ T cells implying the existence of a specialised immune cell network in immune-privileged testis compared with accessory glands.

In line with their CD44hiCD27RORγt+ phenotype, we found that testicular γδ T cells produce IL-17 after ex vivo stimulation, and are in fact the main producers of this pro-inflammatory cytokine among all lymphocytes, whereas αβ T cells almost mostly secrete IFN-γ in the testis. Importantly, we observed a so-far-unknown expansion of murine testicular IL-17-producing Vγ6+ γδ T cells during puberty, around the age of 5 and 7 weeks. This dramatic accumulation of a cell population known to develop exclusively in the embryonic period16 led us to investigate the underlying mechanisms. At puberty, the testicular microenvironment is defined by specific changes in tissue structure, sexual hormones and microbiome composition.23 We showed that testicular γδ T cells depend on microbial signals and the TLR4–MYD88–IL-1α/IL-23 signalling axis. Interestingly, in contrast with the prominent role of IL-1β in the induction of IL-17 production by γδ T cells in the inflamed CNS,32 we show that testicular γδ17 cell homoeostasis at steady state is dependent on IL-1α. IL-1α is mainly produced by Sertoli and germ cells, and was previously shown to promote growth of immature Sertoli and spermatogonia cells,40,41 to inhibit Leydig cell steroidogenesis42 and to regulate blood–testis barrier dynamics by affecting actin skeleton of Sertoli cells.43 Thus, our work adds an immune-regulatory function of IL-1α within the testicular interstitial space, which is seemingly dependent on the microbiota.

Consistently, microbial cues have been previously reported to regulate γδ17 cell homoeostasis in other tissues, including the gut,44 skin,35 lung,36,45 liver28 and gingiva.29 Moreover, it was recently proposed that bacteria can also reside in organs assumed to be sterile and immune-privileged, such as the retina, where they promote IL-17 production by γδ T cells.37 Hence, it is conceivable that the testis itself could also harbour a resident microbiota that could modulate and shape testicular immune responses. Further investigations will be required to test this hypothesis.

On the other hand, it would be very interesting to identify the initial time point when foetal-derived γδ T cells migrate to the testis as well as molecules or stimuli required for the accumulation/expansion of these cells upon puberty.16 However, in this study, we observed that even in the absence of germs, TLR4, MYD88, IL-1R or IL-23R, a small population of Vγ6+ or γδ17 cells is still present in the testis. Therefore, we speculated that the initial development, but not the accumulation/expansion within the tissue, depends on microbial stimuli. Previously, it was shown that CCR6 promotes the migration of Vγ6+ γδ T cells to tissues at steady state.22 However, CCR6 was only expressed by a small fraction of testicular γδ17 cells, suggesting that other chemokines could be involved in their recruitment, while we also cannot formally exclude a downregulation of CCR6 expression after driving migration. Besides recruitment, in situ proliferation could thus also contribute to the increase in γδ T-cell numbers upon puberty. In line with this, we observed that Vγ6+ γδ T cells strongly proliferated in the pubertal testis, as mainly all of these cells expressed the proliferation marker Ki67. This substantial population then persisted throughout adulthood. In accordance, we found a reduced proliferative capacity of this cell subset after puberty and, moreover, tissue-resident Vγ6+ γδ T cells are characterised by their longevity.46

So what might be the physiological function of γδ17 cells in the testis? In vivo imaging revealed their motile, tissue-screening behaviour, which points to a role in tissue surveillance. Furthermore, we speculated that innate-like γδ T cells might be especially important for the fast–immune response against invading pathogens within the testis. The function of IL-17-secreting γδ T cells is already described in other immune-privileged sites, where they are associated with enhanced disease severity in stroke and experimental autoimmune encephalitis (EAE) within the brain,47,48 or increased protection against bacterial and fungal infection in the eye.37 Hence, rapid IL-17 production within the testis might be similarly important for immune defense against infection with bacteria.49 Interestingly, a unilateral intra-testicular inoculation of L. monocytogenes was shown to induce autoimmune-induced inflammation in the contralateral testis without spread of bacteria.11 While αβ T cells and macrophages play a detrimental role in the infected testis, Vγ6+ γδ T cells were shown to protect both infected and non-infected testis by producing IFN-γ, IL-2, IL-10 and TGF-β.11,12 Accordingly, we observed that intra-testicular infection with L. monocytogenes led to an infiltration of αβ and γδ T cells, in particular of IFN-γ-producing cells. This goes in line with previous data demonstrating that IFN-γ produced by neutrophils, NK or T cells upon L. monocytogenes infection promotes macrophage recruitment and consequently bacterial clearance and tissue.50 This crucial role of IFN-γ in the initial phase of L. monocytogenes infection is clearly demonstrated by the poor survival of Ifnγ−/ mice. On the other hand, Tcrδ−/− and Il17−/ mice survived to the same dose of infection although displaying a higher bacterial load in the testis compared with WT controls. Interestingly, and in agreement with a previous study on the female reproductive tract,51 our results suggest that γδ17 cells boost the production of IFN-γ in situ and/or the recruitment of IFN-γ-producing subsets. Therefore, IL-17 seemingly promotes an amplification loop of the inflammatory response upon infection, as previously reported in EAE.52 Importantly, we observed very high susceptibility of Il17−/− and Tcrδ–/− mice to high (4 × 103 CFU) doses of L. monocytogenes, which firmly establishes the protective role of mucosal γδ17 cells against bacterial infection in situ. Along the same line, recent findings have reported a protective role for Vγ6+ γδ T cells against Candida albicans in the female reproductive tract.39 Together, these examples may serve as a proof of concept for an antimicrobial immune surveillance of mucosal γδ17 cells in the male and female reproductive organs, predicting a similar response to other pathogens, such as Escherichia coli (E. coli) or Chlamydia, although further investigation will be needed to test this hypothesis.

In sum, we demonstrate that γδ17 cells are part of the immune system of the testis at steady state; they expand at puberty and make an important contribution to local tissue immune surveillance.

Methods

Mice

C57BL/6, TcrdH2BeGFP, B6-Trcdtm1MalRag1tm1.1Sadu Gt(ROSA)26Sortm1 (creERT2)Tyj (here: Indu-Rag1×TcrdH2BeGFP),53 C57BL/6-Il23rtm1Kuch (here Il23rgfp/gfp or Il23rgfp/+), Il23r−/−, Il1r−/−, Il1β/−, Il1α/−, Myd88−/−, Tlr2–/− and Tlr4/, Tcrδ−/− and Il17a–/– (referred as Il17−/−) and Il17aeGFP × Il22sgBFP reporter18 mice were kept in the Central Animal Facility at Hannover Medical School or Instituto de Medicina Molecular—João Lobo Antunes. When possible, Tcrδ−/ and Il17−/− mice were compared with their littermate controls that were co-housed from birth until weaning. WT germ-free (GF) mice were maintained in the Central Animal Facility at Hannover Medical School or in the GF facility of IGC (Oeiras, Portugal). Animals were purchased from Charles River or from the Jackson Laboratory. The cages are individually ventilated, so the animals were maintained under specific pathogen-free conditions. All experiments were approved by the animal ethics committee at the institutes and performed according to national and European regulations. For experiments 3–14-week-old males were sacrificed by CO2 inhalation and cervical dislocation. Testes, prostates and seminal vesicles were harvested after opening the abdomen from male mice.

Haematoxylin and eosin staining

Frozen sections (5 µm) of mouse testis, prostate and seminal vesicle were fixed in ice-cold acetone for 10 min. The sections were stained with haematoxylin for 10 min and eosin for 30 s. After washing, slides were analysed by bright-field microscopy using a motorised upright Olympus BX61 fluorescence microscope with a ×10//0.4 objective (UPlanSApo, Olympus) and a F-View II camera (Olympus). Images were utilised by cellSens Dimension Software 1.12 (Olympus).

Immunohistology

Frozen sections (7 µm) of mouse testis, prostate and seminal vesicle were fixed in ice-cold acetone for 10 min. After rehydration for 10 min and washing in TBST buffer, slides were blocked with 10% mouse serum diluted in TBST for 10 min. Next, the sections were incubated with diluted primary antibody anti-CD3 (Cy3, 17A2, in-house production with rat hybridoma cell lines), for 1 h at room temperature. After washing three times with TBST, the sections were stained either with diluted secondary antibody anti-rabbit IgG (Cy5, Jackson) for 45 min or with diluted DAPI for 3 min. The slides were washed two times with TBST. Sections were analysed by immunofluorescence microscopy using the previously described Olympus fluorescence microscope with Colour View IIIu camera (Olympus) and cellSens Dimension Software 1.12 (Olympus).

Two-photon laser-scanning microscopy

For ex vivo imaging, extracted testes of TcrdH2BeGFP reporter mice were immobilised in an imaging chamber, which was flushed with oxygenated (95% O2/5% CO2) RPMI-1640 medium (Invitrogen) containing 1% penicillin/streptomycin, 25 mM HEPES and 5 g/litre glucose. The TriM Scope (LaVision BioTec) equipped with an upright Olympus BX51 microscope with a 203/0.95 water-immersion objective and a pulsed Ti sapphire-infrared laser (Mai Tai, SpectraPhysics) turned to 920 nm was used for imaging. The Imaris software 7.7.2 (Bitplane) was used for data analysis.

Cell preparation for flow cytometry

Single-cell suspensions from testis, prostates and seminal vesicles were prepared by dissection of organs with a scalpel and incubation in 0.25 mg/ml collagenase D and 0.025 mg/ml DNase in RPMI-1640 medium with 10% FCS at 37 °C for 1 h. Digested solutions were passed through a 100-µm cell strainer, and lymphocytes were isolated by using a density-gradient centrifugation on 40% and 70% Percoll or Lympholyte. Cell suspensions were stained for flow-cytometry analysis using the following antibodies after blocking with 5% or 10% FC block: antibodies against CD45.2 (APCeF670, 104), CD44 (APC, IM7), CD3e (PECy7, 145-2C11), rat-IgM (PE, RM7B4), IL-17A (eFluor660, eBio17B7), CD69 (APC, H1.2F3), RORγt (APC, AFKJS-9) and T-bet (PE, eBio4B10) were purchased from eBioscience, antibodies against Tcrβ (PeCy7, H57-597), CD27 (PerCPCy5.5, LG.3A10), γδTCR (APC, GL3), Vγ1 (PE, 2.11), Vγ4 (PE, UC3-10A69), IL-17 (PE and PECy7, TC11-18H10.1), CD4 (BV605, RM-4.5) and CD8 (BV711, 53-6.7) were obtained from Biolegend, antibodies against CD45.2 (VioGreen, 104-2), CD3e (APCVio770 and VioBlue, 145-2C11), Tcrβ (APCVio700 and PerCPVio700, REA318), CD44 (VioBlue, IM7.8.1) and γδTCR (PEVio770, REA633) were purchased from Miltenyi, antibodies against CD3e (PE, 145-2C11), CCR6 (A647, 140706) Vγ5 (APC, 536) and ki67 (PECy7, B56) were obtained from BD Biosciences, antibody against IFN-γ (PECy7, XMG1.2) was ordered from Thermo Fisher Scientific and antibodies against Vγ4 (Cy5, 49-2.1), γδTCR (Alexa488, GL3) and 17D1 were produced in-house with rat hybridoma cell lines.

To check the viability, cells were stained either with Zombie Aqua Dead Cells or LiveDead Fixable Viability Dye (Invitrogen) before blocking or with DAPI after surface staining. Samples were acquired using LSRII (BD Biosciences) or FACSFortessa (BD Biosciences). Data were analysed using FlowJo software (Tree Star).

Cytokine measurement

Before staining for intracellular cytokines, isolated single cells were stimulated in 96-well plates in RPMI-1640 medium (containing 1% glutamine (100×), 1% PenStrep and 10% FCS) with PMA (final concentration 50 ng/ml) and ionomycin (final concentration 2 µg/ml) and incubated for 3 h at 37 °C with Brefeldin A (final concentration 10 µg/ml). Cells were stained for surface molecules and then treated with Cytofix/Cytoperm according to the manufacturer’s protocol (BD Biosciences). Ultimately, cells were stained for intracellular IL-17 and IFN-γ.

Spermatogenesis assay

Testicular preparations were isolated using a two-step enzymatic digestion to remove interstitial cells, as previously described.54 Briefly, the testis tunica albuginea was removed, and seminiferous tubules were dissociated by enzymatic digestion with 0.5 mg/ml of collagenase D (Roche) and 200 μg/ml DNAseI (Roche) for 20 min at 35 °C in complete DMEM: F12 (Invitrogen), supplemented with 1 mM L-glutamine, 5 mM sodium L-lactate, 1 mM sodium pyruvate and 0.1 mM MEM nonessential amino acids (all from Invitrogen Life Technologies). The suspension was layered over 5% Percoll gradient (GE Healthcare) and allowed to settle for 20 min. The bottom Percoll composed of interstitial cell was digested with 200 μg/ml DNaseI and 1 mg/ml trypsin for 20 min at 35 °C, and foetal bovine serum (FBS) was added to halt the digestion. The digested product was filtered through a 70-μm and a 40-μm cell strainer, washed in PBS and centrifuged at 500 × g for 10 min, and the resulting pellet was resuspended in complete DMEM:F12 supplemented with 5% FBS. Cell suspensions was stained with 7AAD for 1 h at 4 °C for analyses of the cell cycle. Testicular cell population was referred as 4 N (tetraploid testicular cells, premeiotic spermatocyte I), 2 N (diploid testicular cells) and N (haploid spermatids).

Enzyme-linked immunosorbent assay (ELISA)

Levels of testosterone (R&D System) from serum and levels of IL-1α, IL-23 and IL-1β (Invitrogen) from the testis were measured by ELISA, according to the manufacturer’s instructions. Blood was removed from the heart, settled for 30 min at room temperature and centrifuged at 15,000 × g for 10 min at RT. Serum supernatant was collected and stored at −20 °C until used. Total protein content was quantified using the BioRad DC Protein Assay kit.

RNA isolation, cDNA production and real-time PCR

For mRNA expression analysis, total RNA was extracted with the high pure RNA isolation kit (Roche), according to the manufacturer, from sorted γδ T cells, CD4 T cells, CD8 T cells, monocytes, dendritic cells, neutrophils or enriched Sertoli and Leydig cells, as previously described.54 RNA concentration and purity were determined using the NanoDropTM 2000 spectrophotometer (Thermo Fisher Scientific).

For mRNA, reverse transcription was performed with random oligonucleotides (Invitrogen) using Moloney murine leukemia virus reverse transcriptase (Promega). The total RNA was reverse-transcribed into cDNA using the T100® Thermal Cycler (BioRad), and all quantitative PCRs (qPCRs) were performed in MicroAmp® Optical 384-Well Reaction Plate (Applied Biosystems) using the RT-PCR ViiA7TM system (Applied Biosystems). For mRNA expression analysis, primer sets (Sigma) designed by Universal Probe Library Assay Design Center (Roche) were used on the cDNA previously obtained, and relative quantification of specific cDNA species to endogenous references Beta-Actin or Beta2-microglobulin was carried out using SYBR on ViiA7 cycler (Applied Biosystems). Data were analysed using ViiA7TM software v1.2.1.

Listeria monocytogenes infection

Nine- to 12-week-old male mice were used for the experiments (L. monocytogenes strain EGD). Mice were inoculated into both testes under the tunica albuginea with 2 × 103 or 4 × 103 colony-forming units (CFU) of L. monocytogenes in 20 µL of PBS.

Statistical analysis

Statistical analysis was performed using Graphpad Prism. The values presented are mean ± SD of n independent experiments. To test the significance of the differences between two conditions, a Student’s t test and Mann–Whitney were used. P values of <0.05 were considered to be statistically significant. Statistical analyses are described in more detail in figure legends.

References

  1. 1.

    Fijak, M. & Meinhardt, A. The testis in immune privilege. Immunol. Rev. 213, 66–81 (2006).

    CAS  PubMed  Google Scholar 

  2. 2.

    Tung, K. S. K. et al. Egress of sperm autoantigen from seminiferous tubules maintains systemic tolerance. J. Clin. Invest. 127, 1046–1060 (2017).

    PubMed  PubMed Central  Google Scholar 

  3. 3.

    Wang, M. et al. Characterization of the micro-environment of the testis that shapes the phenotype and function of testicular macrophages. J. Immunol. 198, 4327–4340 (2017).

    CAS  PubMed  Google Scholar 

  4. 4.

    Hales, D. B. Testicular macrophage modulation of Leydig cell steroidogenesis. J. Reprod. Immunol. 57, 3–18 (2002).

    CAS  PubMed  Google Scholar 

  5. 5.

    Redgrove, K. A. & McLaughlin, E. A. The role of the immune response in Chlamydia trachomatis infection of the male genital tract: a double-edged sword. Front. Immunol. 5, 534 (2014).

  6. 6.

    Prinz, I., Silva-Santos, B. & Pennington, D. J. Functional development of γδ T cells. Eur. J. Immunol. 43, 1988–1994 (2013).

    CAS  PubMed  Google Scholar 

  7. 7.

    Hayday, A. C. γδ T cells and the lymphoid stress-surveillance response. Immunity 31, 184–196 (2009).

    CAS  PubMed  Google Scholar 

  8. 8.

    Pinget, G. V. et al. The majority of murine γδ T cells at the maternal-fetal interface in pregnancy produce IL-17. Immunol. Cell Biol. 94, 623–630 (2016).

    CAS  PubMed  Google Scholar 

  9. 9.

    Song, Z.-H. et al. Seminal plasma induces inflammation in the uterus through the γδ T/IL-17 pathway. Sci. Rep. 6, 25118 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Anipindi, V. C. et al. IL-17 production by γδ + T cells is critical for inducing T h 17 responses in the female genital tract and regulated by estradiol and microbiota. ImmunoHorizons 3, 317–330 (2019).

    CAS  PubMed  Google Scholar 

  11. 11.

    Mukasa, A., Lahn, M., Pflum, E. K., Born, W. & O’Brien, R. L. Evidence that the same gamma delta T cells respond during infection-induced and autoimmune inflammation. J. Immunol. 159, 5787–5794 (1997).

    CAS  PubMed  Google Scholar 

  12. 12.

    Mukasa, A. et al. Bacterial infection of the testis leading to autoaggressive immunity triggers apparently opposed responses of αβ and γδ T cells. J. Immunol. 155, 2047–2056 (1995).

    CAS  PubMed  Google Scholar 

  13. 13.

    Munoz, G., Posnett, D. N. & Witkin, S. S. Enrichment of γδ T lymphocytes in human semen: relation between γδ T cell concentration and antisperm antibody status. J. Reprod. Immunol. 22, 47–57 (1992).

    CAS  PubMed  Google Scholar 

  14. 14.

    Azenabor, A., Ekun, A. O. & Akinloye, O. Impact of inflammation on male reproductive tract. J. Reprod. Infertil. 16, 123–129 (2015).

    PubMed  PubMed Central  Google Scholar 

  15. 15.

    Carding, S. R. & Egan, P. J. γδ T cells: functional plasticity and heterogeneity. Nat. Rev. Immunol. 2, 336–345 (2002).

  16. 16.

    Haas, J. D. et al. Development of interleukin-17-producing γδ T cells is restricted to a functional embryonic wave. Immunity 37, 48–59 (2012).

    CAS  PubMed  Google Scholar 

  17. 17.

    Ribot, J. C. et al. CD27 is a thymic determinant of the balance between interferon-gamma- and interleukin 17-producing gammadelta T cell subsets. Nat. Immunol. 10, 427–436 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Perez, L. G. et al. TGF-β signaling in Th17 cells promotes IL-22 production and colitis-associated colon cancer. Nat. Commun. 11, 1–14 (2020).

  19. 19.

    Ono, T. et al. IL-17-producing γδT cells enhance bone regeneration. Nat. Commun. 7, 1–9 (2016).

    Google Scholar 

  20. 20.

    Kohlgruber, A. C. et al. γδ T cells producing interleukin-17A regulate adipose regulatory T cell homeostasis and thermogenesis /631/250/256 /631/250/2504 article. Nat. Immunol. 19, 464–474 (2018).

    CAS  PubMed  Google Scholar 

  21. 21.

    Ribeiro, M. et al. Meningeal γδ T cell-derived IL-17 controls synaptic plasticity and short-term memory. Sci. Immunol. 4, eaay5199 (2019).

  22. 22.

    McKenzie, D. R. et al. IL-17-producing γδ T cells switch migratory patterns between resting and activated states. Nat. Commun. 8, 1–13 (2017).

    Google Scholar 

  23. 23.

    Plant, T. M. et al. Knobil and Neill’s Physiology of Reproduction (Elsevier Academic Press, Amsterdam, 2015).

  24. 24.

    Yurkovetskiy, L. et al. Gender bias in autoimmunity is influenced by microbiota. Immunity 39, 400–412 (2013).

    CAS  PubMed  Google Scholar 

  25. 25.

    Markle, J. G. M. et al. Sex differences in the gut microbiome drive hormone-dependent regulation of autoimmunity. Science. 339, 1084–1088 (2013).

    CAS  PubMed  Google Scholar 

  26. 26.

    Ivanov, I. I. et al. Induction of intestinal Th17 cells by segmented filamentous bacteria. Cell 139, 485–498 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Benakis, C. et al. Commensal microbiota affects ischemic stroke outcome by regulating intestinal γδ T cells. Nat. Med. 22, 516–523 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  28. 28.

    Li, F. et al. The microbiota maintain homeostasis of liver-resident γδ T-17 cells in a lipid antigen/CD1d-dependent manner. Nat. Commun. 7, 1–14 (2017).

    Google Scholar 

  29. 29.

    Wilharm, A. et al. Mutual interplay between IL-17-producing γδT cells and microbiota orchestrates oral mucosal homeostasis. Proc. Natl Acad. Sci. USA 116, 2652–2661 (2019).

    CAS  PubMed  Google Scholar 

  30. 30.

    Iwasaki, A. & Medzhitov, R. Regulation of adaptive immunity by the innate immune system. Science 327, 291–295 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  31. 31.

    Ribot, J. C. et al. Cutting edge: adaptive versus innate receptor signals selectively control the pool sizes of murine IFN-γ- or IL-17-producing γδ T cells upon infection. J. Immunol. 185, 6421–6425 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  32. 32.

    Sutton, C. E. et al. Interleukin-1 and IL-23 induce innate IL-17 production from gammadelta T cells, amplifying Th17 responses and autoimmunity. Immunity 31, 331–341 (2009).

    CAS  PubMed  Google Scholar 

  33. 33.

    Mukasa, A., Yoshida, H., Kobayashi, N., Matsuzaki, G. & Nomoto, K. γδ T cells in infection-induced and autoimmune-induced testicular inflammation. Immunology 95, 395–401 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  34. 34.

    Sandrock, I. et al. Genetic models reveal origin, persistence and nonredundant functions of IL-17-producing γδ T cells. J. Exp. Med. 215, 3006–3018 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Gray, E. E., Suzuki, K. & Cyster, J. G. Cutting edge: identification of a motile IL-17–producing γδ T cell population in the dermis. J. Immunol. 186, 6091–6095 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Misiak, A., Wilk, M. M., Raverdeau, M. & Mills, K. H. G. IL-17–producing innate and pathogen-specific tissue resident memory γδ T cells expand in the lungs of Bordetella pertussis-infected mice. J. Immunol. https://doi.org/10.4049/jimmunol.1601024 (2017).

  37. 37.

    St. Leger, A. J. et al. An ocular commensal protects against corneal infection by driving an interleukin-17 response from mucosal γδ T cells. Immunity 47, 148–158.e5 (2017).

    PubMed Central  Google Scholar 

  38. 38.

    Palomino-Segura, M., Latino, I., Farsakoglu, Y. & Gonzalez, S. F. Early production of IL-17A by γδ T cells in the trachea promotes viral clearance during influenza infection in mice. Eur. J. Immunol. 50, 97–109 (2020).

    CAS  PubMed  Google Scholar 

  39. 39.

    Monin, L. et al. γδ T cells compose a developmentally regulated intrauterine population and protect against vaginal candidiasis. Mucosal Immunol. 1–13, https://doi.org/10.1038/s41385-020-0305-7 (2020).

  40. 40.

    Pöllänen, P., Söder, O. & Parvinen, M. Interleukin-la stimulation of spermatogonial proliferation in vivo. Reprod. Fertil. Dev. 1, 85–87 (1989).

    PubMed  Google Scholar 

  41. 41.

    Petersen, C., Boitani, C., Fröysa, B. & Söder, O. Interleukin-1 is a potent growth factor for immature rat Sertoli cells. Mol. Cell. Endocrinol. 186, 37–47 (2002).

    CAS  PubMed  Google Scholar 

  42. 42.

    Svechnikov, K. V., Sultana, T. & Söder, O. Age-dependent stimulation of Leydig cell steroidogenesis by interleukin-1 isoforms. Mol. Cell. Endocrinol. 182, 193–201 (2001).

    CAS  PubMed  Google Scholar 

  43. 43.

    Sarkar, O., Mathur, P. P., Cheng, C. Y. & Mruk, D. D. Interleukin 1 alpha (IL1A) is a novel regulator of the blood-testis barrier in the Rat1. Biol. Reprod. 78, 445–454 (2008).

    CAS  PubMed  Google Scholar 

  44. 44.

    Ismail, A. S., Behrendt, C. L. & Hooper, L. V. Reciprocal interactions between commensal bacteria and γδ intraepithelial lymphocytes during mucosal injury. J. Immunol. 182, 3047–3054 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Cheng, M. et al. Microbiota modulate tumoral immune surveillance in lung through a γδT17 immune cell-dependent mechanism. Cancer Res. 74, 4030–4041 (2014).

    CAS  PubMed  Google Scholar 

  46. 46.

    Tan, L. et al. Single-cell transcriptomics identifies the adaptation of Scart1+ Vγ6+ T cells to skin residency as activated effector cells. Cell Rep. 27, 3657–3671.e4 (2019).

    CAS  PubMed  Google Scholar 

  47. 47.

    Blink, S. E. et al. γδ T cell subsets play opposing roles in regulating experimental autoimmune encephalomyelitis. Cell. Immunol. 290, 39–51 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  48. 48.

    Arunachalam, P. et al. CCR6 (CC chemokine receptor 6) is essential for the migration of detrimental natural interleukin-17-producing γδ T cells in stroke. Stroke 48, 1957–1965 (2017).

    CAS  PubMed  Google Scholar 

  49. 49.

    Anders, H. J. & Patole, P. S. Toll-like receptors recognize uropathogenic Escherichia coli and trigger inflammation in the urinary tract. Nephrol. Dial. Transplant. https://doi.org/10.1093/ndt/gfh922 (2005).

  50. 50.

    Wang, G. et al. IFN-γ protects from apoptotic neutrophil-mediated tissue injury during acute Listeria monocytogenes infection. Eur. J. Immunol. 48, 1470–1480 (2018).

    CAS  PubMed  Google Scholar 

  51. 51.

    Bagri, P. et al. Novel role for interleukin-17 in enhancing type 1 helper t cell immunity in the female genital tract following mucosal herpes simplex virus 2 vaccination. J. Virol. https://doi.org/10.1128/jvi.01234-17 (2017).

  52. 52.

    Pikor, N. B. et al. Integration of Th17- and lymphotoxin-derived signals initiates meningeal-resident stromal cell remodeling to propagate neuroinflammation. Immunity 43, 1160–1173 (2015).

    CAS  PubMed  Google Scholar 

  53. 53.

    Düber, S. et al. Induction of B-cell development in adult mice reveals the ability of bone marrow to produce B-1a cells. Blood 114, 4960–4967 (2009).

    PubMed  Google Scholar 

  54. 54.

    Chang, Y. F., Lee-Chang, J. S., Panneerdoss, S., MacLean, J. A. & Rao, M. K. Isolation of sertoli, leydig, and spermatogenic cells from the mouse testis. Biotechniques 51, 341–344 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We thank the precious assistance of the staff of the Flow Cytometry, Histology and Rodent facilities of iMM and Hannover Medical School; Bruno Silva-Santos for insightful suggestions and critical reading of the paper; Natacha Gonçalves-Sousa, Afonso Almeida, Pedro Papotto, Miguel Muñoz‐Ruiz, Francisco Caiado, Karine Serre, Sofia Mensurado, Julie Darrigues, Sara Pereira, Gina Fiala, Gisela Gordino, André Simoes, Daniel Inacio, Carolina Cunha, Afonso Antunes, Daniel Gomes da Costa (iMM Lisboa, Portugal), Andreas Krueger, Daniel J. Pennington (Blizard Institute, Queen Mary, London, UK), Adrian Hayday (The Francis Crick Institute, London, UK), Youenn Jouan and Christophe Paget (INSERM, Tours, France) for helpful discussions and technical support. We are also grateful to Siggi Weiß for provision of Indu-Rag1 mice, Thomas Korn for Il23rgfp/gfp mice, Mohammed Oukka (University of Washington, USA) and Fiona Powrie (Oxford University, UK) for Il23r−/− mice, Shizuo Akira (Osaka University, Japan) for Myd88–/– mice and Instituto Gulbenkian de Ciência for Il1α−/−, Il1β−/−, Il1r−/− and GF mice. Funding: This work was funded by the Fundação para a Ciência e Tecnologia (IF/00013/2014 to J.C.R., PD/BD/114103/2015 to H.C.B.), and by the Deutsche Forschungsgemeinschaft (DFG) grants PR727/8-1 and PR727/11-1 to I.P.; A.W. was a scholar of Hannover Biomedical research School. This publication was supported by UID/BIM/50005/2019, a project funded by Fundação para a Ciência e a Tecnologia (FCT)/Ministério da Ciência, Tecnologia e Ensino Superior (MCTES) through Fundos do Orçamento de Estado.

Author information

Affiliations

Authors

Contributions

A.W. and H.C.B. performed most of the experiments, analysed the data and contributed to the paper writing; I.S., M.R., T.A., A.R., A.D., L.H. and T.S. assisted in the experiments; T.C. performed the histology analysis; I.P. and J.C.R. designed the study, supervised the research and wrote the paper.

Corresponding authors

Correspondence to Immo Prinz or Julie C. Ribot.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Wilharm, A., Brigas, H.C., Sandrock, I. et al. Microbiota-dependent expansion of testicular IL-17-producing Vγ6+ γδ T cells upon puberty promotes local tissue immune surveillance. Mucosal Immunol (2020). https://doi.org/10.1038/s41385-020-0330-6

Download citation