Putative link between Polo-like kinases (PLKs) and Toll-like receptor (TLR) signaling in transformed and primary human immune cells

Toll-like receptors (TLRs) are important sentinels of bacterial and viral infection and thus fulfil a critical sensory role in innate immunity. Polo-like kinases (PLKs), a five membered family of Ser/Thr protein kinases, have long been studied for their role in mitosis and thus represent attractive therapeutic targets in cancer therapy. Recently, PLKs were implicated in TLR signaling in mice but the role of PLKs in TLR signaling in untransformed primary immune cells has not been addressed, even though PLK inhibitors are in clinical trials. We here identified several phospho-serine and phospho-threonine residues in the known TLR pathway kinases, Interleukin-1 receptor-associated kinase (IRAK) 2 and IRAK4. These sites lie in canonical polo-box motifs (PBM), sequence motifs known to direct recruitment of PLKs to client proteins. Interestingly, PLK1 was phosphorylated and PLK 2 and 3 mRNA induced upon TLR stimulation in primary immune cells, respectively. In whole blood, PLK inhibition disparately affected TLR mediated cytokine responses in a donor- and inhibitor-dependent fashion. Collectively, PLKs may thus potentially interface with TLR signaling in humans. We propose that temporary PLK inhibitor-mediated blockade of TLR-signaling in certain patients receiving such inhibitors during cancer treatment may cause adverse effects such as an increased risk of infections due to a then compromised ability of the TLR recognition system to sense and initiate cytokine responses to invading microbes.

IRAK2 DD protein-protein interactions 5 . Work by us and others showed that naturally occurring loss-of-function mutations in MyD88 prevent Myddosome formation 6 and suggest that the Myddosome is a critical post-receptor complex in innate immunity 7 . The IRAK kinase domain (KD) activity is switched on first in IRAK4 then IRAK1 or 2 upon Myddosome formation and initiates the subsequent steps of downstream signaling such as the ubiquitination of TNF receptor-associated factor (TRAF) 6. TRAF6 ubiquitination is sensed by the ubiquitin binding regulatory TAB2/TAB3 subunits of the TAK1 complex which subsequently initiates MAPK and IKKα/β activation 8 . One hallmark of the multi-faceted gene transcription programs regulated by the transcription factors activated by MAPK and IKK, namely AP-1 and NF-κB, is the production of pro-inflammatory cytokines. In some cell types, predominantly plasmacytoid dendritic cells (pDC), MyD88-IRAK-dependent signaling activates IFN regulatory factors (IRF) which are important for type I IFN induction. Thus through triggering expression of pro-inflammatory cytokines such as IFNs, TLRs shape courses of infections 1 . Recent data also point to an involvement of MyD88-dependent signaling in the context of non-Hodgkin lymphomas, where MYD88 gain-of-function mutations promote tumor cell growth 9 . Thus it is of interest to characterize modulators of these signaling events for therapeutic intervention.
Recently an intriguing link between TLR signaling and Polo-like kinases (PLKs) was reported 10 . The human PLK family includes five members, PLK1-5. Especially PLK1 has been extensively studied in the context of cell cycle regulation. In cell cycle regulation, PLK1 cooperates with cyclin-1 dependent kinase 1, cyclin B1 and Aurora kinase and is involved in centrosome maturation, G2/M transition, kinetochore function, mitotic exit and cytokinesis. The roles of other PLKs are more enigmatic but implication as tumor suppressors by interaction with the p53 signaling network have been proposed. PLKs canonically consist of an N-terminal KD and a C-terminal so-called Polo-box domain (PBD) 11 . It is believed that the PBD directs PLKs to substrate molecules by binding to conserved so-called Polo box motif (PBM), typically comprised of Ser-pThr-Pro or Ser-pSer-Pro (SpSP/SpTP) 12 . Binding of the PBD to PBM sequences is then thought to relieve PLK KD inhibition and activate PLK kinase activity. In the context of cell division, many PBM-containing PLK binding partners have been described and proteomics screens identified >600 proteins that interact with PLK1. In the context of cell division, PBM motifs are "generated" through phosphorylation of SSP and STP sequences by cyclin-dependent kinases (CDKs) 13 . Their essential requirement in cell division has given rise to the notion that PLKs constitute attractive targets for cancer therapy (see ref. 14 and www.clinicaltrial.gov). Inhibition of PLKs resulted in an abortive cell cycle and drive cancer cells into apoptosis 14 . Inhibitors such as BI2536, BI6727 (Volasertib) and GSK461364 have been reported to possess nanomolar IC50 values and target PLK1 KD activity 14 . Fewer approaches have targeted the PBD of PLK1, for example poloxin 14 . The specificity of PBD-targeting inhibitors for PLK1 varies but most inhibitors also affect other PLKs, so that the efficacy of PLK1 inhibitors could at least partially result from additional effects on other PLKs, e.g. PLKs 2 to 4 for which off-target effects of PLK1 inhibitors were reported 14 . Several published academia-and industry-driven phase I and II clinical studies using the abovementioned compounds so far show good tolerability, limited side-effects and promising results in terms of efficacy in non-small cell lung cancer and non-Hodgkin lymphoma [15][16][17] . Thus PLK inhibitors may be licensed for use in humans at some stage in the near future.
Unfortunately, possibly due to the fact that homozygous PLK1 mice are not viable, relatively little is known about the role of PLK1 in processes other than cell cycle regulation. The same applies to other PLKs. However, a recent report by Chevrier et al. identified PLK2 and 4 in an siRNA screen to be involved in TLR signaling in murine cells and PLK1 inhibitors recapitulated the effects observed by PLK2 and 4 knock-down 10 . Specifically, BI2536 blocked transcription of antiviral genes such as Ifnb1, Cxcl10 and Cxcl1. Unfortunately, the situation in human primary immune cells was not addressed. Other groups reported that PLK1 interacted with NEMO (also known as IKKγ) via the scaffold protein TANK (also known as TRAF2) affecting NF-κB signaling in HEK293 and K562 cell lines 18 . Additionally, TANK and IKKβ were found to be phosphorylated by PLK1 in proteomics approaches analyzing samples from Hela or COS7 and HEK293 cell lines, respectively 19,20 . It is unknown which upstream signal(s) prompt(s) the recruitment and/or kinase activity of PLK1 in this context and by which mechanism. Prolyl isomerase (PIN) 1 is another substrate and interactor of PLK1 in Hela cells 19 . PIN1 also interacts with murine IRAK1, and this interaction was dependent on phosphorylation sites in the IRAK1 linker region (S131, S144, S173) 21 . Thus PIN1 may act as a bridging molecule between IRAKs and PLKs. On the other hand, PLKs and IRAKs may counter-influence each other through direct interactions although this has not been proven. Collectively, there is some reported evidence for a role of PLKs in several innate immune signaling pathways. However, all of the above reported data in human cells were exclusively generated using immortalized cell lines and thus may potentially be confounded by continuous PLK activation during cell division. Studies using primary cells have so far only been conducted in murine cells 10 . Therefore it is unclear if PLKs do in fact play a role in human primary immune cells.
After identifying PBMs in members of the IRAK family, we sought to gather evidence for a link between PLKs andTLR mediated responses. Here we report the presence of Polo-box-motifs (PBMs) in human IRAK2 and IRAK4 which would enable a mechanistic link between TLR-MyD88-IRAK signaling and PLKs. PLK1 was phosphorylated upon TLR stimulation and PLK2 and 3 gene transcription was found to be upregulated in primary human cells. Additionally, we report that PLK inhibitors may interfere with TLR-mediated cytokine production in whole blood in a donor-dependent way.

Results
Human IRAK2 and IRAK4 harbor Polo-box motifs. In a search for regulatory events in TLR pathways, we investigated phosphorylation sites in the human IRAKs and identified phospho-serine 144 (S144) by mass spectrometry of recombinant IRAK2 protein purified from mammalian cells (HEK293T) (Fig. 1A,B). S144 maps to the linker region between the IRAK2 DD and KD (red box in Fig. 1A). The sequence of this linker region is not related to linker regions of the other three IRAK orthologues. Furthermore S144 of IRAK2 is only present in homologues from humans and primates but not in mice. We could also identify several probable auto-phosphorylation sites in IRAK4 after it was purified from E. coli, using a buffer composition and ATP concentration that are conducive to the recombinant protein developing kinase activity. This IRAK4 protein was subjected to tryptic digest and analyzed by mass spectrometry(MS). More than 20 new phospho-sites were identified ( Fig. 1C) and two of these (S8, T62) when mutated affected the interaction of IRAK4 with MyD88 as shown elsewhere 22 . The newly identified phospho-sites included S152 (red box in Fig. 1C). When inspecting these sites more closely, we noted that pS144 in IRAK2 and pS152 in IRAK4 are part of hitherto unrecognized PBMs, both SpSP (red boxes in Fig. 1A,C). Interestingly, both phospho-sites map to the linker regions connecting DD and KD the structural conformation of which regulates activity in murine Irak1 21 . Primary sequence analysis identified several additional putative PBMs in human IRAKs: in IRAK1 residues 399-401 (S400 is also phosphorylated, not shown); and in the IRAK2 KD at position 275-277 (phosphorylation status of S276 unknown to date, Fig. 1C). To gain a first insight into whether these sites are phosphorylated and possibly regulated in immune cells, we stimulated THP-1 macrophage-like cells with the TLR2 ligand, Pam 2 CSK4, a synthetic deacetylated lipopeptide (here referred to as Pam2), for 30 min and conducted a preliminary phospho-proteomics experiment, analyzing www.nature.com/scientificreports www.nature.com/scientificreports/ changes in phospho-peptides concerning IRAK1, 2 and 4. Pam2 was chosen as it had previously been shown to affected the phospho-status of IRAK1 S402 23 . As shown in Table 1, IRAK1 phospho-peptides encompassing S399, S401 and S402 (and thus the PBM) were identified, in agreement with independent crystallographic and proteomics evidence 24,25 . In stimulated THP-1 cells the sites changed their abundance between 1,8 to >10-fold following Pam2 stimulation compared to unstimulated cells. For IRAK2, a peptide encompassing S143 and S144 was detected. Even though S143 was downregulated approx. 5-fold upon stimulation, S144 was unaltered, indicating it might be a constitutive, not ligand-dependent PBM. IRAK4 S186, T208 and T345 were also confirmed as phospho-residues but not the putative PBM residue S152. The latter was, however, reported in a comprehensive database of phospho-sites, phospho-site.org, in 5 studies that included human primary cellular material [25][26][27][28][29] . Phospho-site.org generally confirmed all PBM sites described here for IRAKs, except S275 in IRAK2 and S186 in IRAK4, see Table 1. The data from THP-1 cells and comprehensive independent evidence from other studies [23][24][25][26][27][28][29][30][31][32][33][34][35][36][37][38] thus suggest that some, if not all, phospho-sites detected here on overexpressed IRAKs in PBMs are potentially physiologically relevant. Since PBMs had not been noted in IRAKs before and the role of Polo kinases in TLR signaling in human primary cells has not been addressed, we took these findings as a starting point for experimentally exploring a possible connection between PLKs and TLR signaling. pLKs are transcribed upon tLR stimulation. Since many TLR pathway signal transducers such as MyD88 are themselves regulated by TLR signaling, we tested whether PLKs were also regulated at the mRNA level in whole blood. Figure 2 shows that treatment of freshly drawn human whole blood with the TLR7/8 agonist R848 or the TLR4 agonist LPS induced cellular PLK2 and PLK3 mRNA levels by approximately 20-fold or 10-fold within 2 h, respectively. For PLK3, mRNA induction remained high up to 6 h whereas PLK2 induction decreased by 6 h. PLK1 and PLK4 were not induced by TLR stimulation. Likewise the TLR3 ligand poly I:C and IL-1 did not induce PLK transcription. This suggests that PLKs may be part of a TLR-elicited feed-forward loop relevant for effector outcomes or to anticipate cellular proliferation. PLK1 is phosphorylated upon TLR stimulation. We next sought to determine whether PLKs are directly activated in response to TLR signaling as well as being transcriptionally upregulated. During mitosis, phosphorylation of PLKs is an indicator of activation 39 . Since there are currently no phospho-specific antibodies for the highly regulated PLKs 2 or 3, we focused on the modification of PLK1 as a representative of the PLK family that has been widely characterized and for which phospho-specific antibodies are available. Whole blood was thus analyzed by anti-phospho-Thr210 flow cytometry 40 after 10 min of R848 stimulation. Figure 3 shows that PLK1 was phosphorylated in gated monocytes, lymphocytes (PBL) and neutrophils (PMN), with monocytes showing the greatest differences in MFI for all donors (n = 3, Fig. 3b). Although further mechanistic details remain to be elucidated, these data suggest that at least PLK1 is activated by TLR triggering and may thus contribute to TLR signal transduction by kinase activity or scaffolding function.

Inhibition of PLK in human primary immune cells disparately affects cytokine induction.
The data so far suggested that PLKs are regulated duringTLR signaling. If indeed this was the case, PLK inhibition may affect TLR mediated cytokine transcription. Given the reported observation for a role of PLK in murine innate immune responses, we sought to test if pharmacological inhibition of PLK kinase activity using BI2536, BI6727 or GSK461364 41 affected the induction of cytokines in response to R848. As shown in Fig. 4, stimulation IRAK4 Q9NWZ3-1 152 n/a n/a n/a n/a n/a n/a n/a n/a n/a YES 25 www.nature.com/scientificreports www.nature.com/scientificreports/ of whole blood from healthy donors with R848 resulted in robust induction of IL6 and CXCL10 mRNA, albeit with high inter-individual variation. Although the effects were moderate and differed between donors, the application of BI2536 led to a dose-dependent reduction in both CXCL10 and IL6 mRNA levels in 2/3 of the donors, in some instances at an inhibitor concentration as low as 1 nM (Fig. 4a). BI6272 (Fig. 4b) and GSK461364 (Fig. 4c) were only analyzed in two donors, donor 2 and 3. Here donor 3 showed an inhibition of cytokine induction for both PLK inhibitors. Donor 2 remained refractory to all inhibitor treatments. Of note, PLK1 inhibitors did not affect another important innate immune signaling machinery, the NLRP3 inflammasome 42 : this was evident when THP-1 cells were treated with PMA and Nigericin, which triggers IL-1β release in these cells 43 . Conversely to a Bruton's Tyrosine Kinase (BTK) inhibitor 44 , PLK inhibitors BI2536, BI6272 and GSK461364 did not block IL-1β release (Fig. 4d) which is regulated transcriptionally by PMA or TLR ligand, and maturation via the NLRP3 inflammasome 45 . Cellular toxicity upon PLK1 inhibition was not observed (Fig. 4e). Although further donors will therefore need to be assessed, our results thus suggest a putative contribution of PLKs to TLR-dependent cytokine responses in certain donors.

Discussion
Over the last decades there has been much interest in exploring PLKs as targets in cancer therapy 14   www.nature.com/scientificreports www.nature.com/scientificreports/ human primary whole blood, a highly physiological system for assessing immune activity, suggest that PLK inhibitors may interfere with TLR-mediated cytokine production in certain subjects. Specifically and in keeping with the data by Chevrier et al., CXCL10 expression was reduced by PLK inhibition in response to TLR agonists 10 . Generally, a sufficient cytokine response is required for efficient immune cell recruitment to sites of infection and the mounting of an adaptive immune response. Thus, PLK inhibition in patients may entail immunosuppression which is a phenomenon observed for many chemotherapeutic drugs, e.g. inhibitors of BTK, a signaling molecule acting downstream of B cell receptor and TLR signaling pathways 46,47 which we recently found to be a direct regulator of the NLRP3 inflammasome 44 . Our data suggest that PLK inhibitors may compromise innate immunity, potentially via a direct effect on TLR signal transduction. Mechanistically, the suppression of PLK kinase activity may have a negative impact on phosphorylation events that promote signaling. At this point we can only speculate whether this will directly affect IRAKs or other pathway members and whether this occurs by PLKs being associated with Figure 3. PLK1 is phosphorylated in primary immune cells upon TLR stimulation. Freshly drawn whole blood was treated with R848 or left untreated for 10 min before erythrocytes were lysed, cells fixed, permeabilized and stained using anti-phospho-PLK1, -p38, -ERK1/2 or -p65. Gates were set to distinguish monocytes, peripheral blood lymphocytes (PBL) and PMN as shown in Fig. S1. Event # are given as indicated. In (a) one representative donor is shown, in (b) data from 2-3 donors are summarized. Each dot represents one donor. Differences were not statistically significant by one-way ANOVA with Sidak correction for multiple testing due to donor-todonor variations and the low number of donors. (2019) 9:13168 | https://doi.org/10.1038/s41598-019-49017-z www.nature.com/scientificreports www.nature.com/scientificreports/ IRAKs either constitutively or only upon TLR signaling. Apart from a role as kinases, it is conceivable that PLK operate as scaffolds that reinforce interactions in post-receptor signaling. The effect of different TLR agonists on PLK1 phosphorylation, the inhibition conferred by PLK blockers, and the occurrence of PBMs in several IRAKs kinases would support the notion that PLKs connect and potentially operate on components of the Myddosome, where TLR pathways converge 6 . IRAKs and PLKs both were shown to separately interact with the prolyl-isomerase PIN1 21,48 , which is also a PLK substrate. A direct interaction or substrate-kinase relationship between endogenously expressed IRAKs and PLKs has, however, yet to be demonstrated are significant limitations of this study. Since . PLK inhibitors BI2536 and BI6272 donor-independently modulate TLR-but not NLRP3 inflammasome-dependent cytokine responses. Freshly drawn whole blood was treated with 5 µg/ml R848 in the presence or absence of the indicated concentrations of BI2536 (a), BI6272 (b) or GSK461364 (c), respectively, for 3 h or left unstimulated. Subsequently, total RNA was isolated, genomic DNA digested, reverse-transcribed and used in quantitative real-time PCR for IL6 and CXCL10 mRNA relative to TBP. Each sample was measured in triplicates and individual symbols represent the mean for each donor coded by symbol type and color.
The effects of inhibition were tested with reference to R848 + DMSO control using an unpaired two-tailed t-test. Technical triplicates that were statistically significantly (p < 0.05) higher or lower than the donor's R848 + DMSO are marked by *. A combined statistical analysis did not yield significant differences due to high inter-individual variation. (d) ELISA analysis of IL-1ß in supernatants from PMA-differentiated THP-1 cells treated for 1 h with the indicated PLK1 inhibitors and then stimulated with the NLRP3 agonist, nigericin. (e) Cell viability using CCK8 reagent normalized to DMSO control. In D and E data are representative of two independent experiments. www.nature.com/scientificreports www.nature.com/scientificreports/ co-overexpression and co-immunoprecipitation in transformed cells, e.g. in HEK293T cells may be confounded by overexpression artefacts, absence of endogenous signaling events or repetitive cell cycling, we attempted to co-immuno-precipitate PLKs and IRAKs from primary monocytes. Unfortunately, this failed in our hands due to the unavailability of specific PLK antibodies to endogenous PLKs Thus further mechanistic work thus remains clearly warranted in future, e.g. studying the effect of the newly identified PBM phospho-sites in IRAK2 and IRAK4 on PLK interactions and TLR post-receptor signaling: Discovering both the kinase(s) phosphorylating the PBMs in IRAKs, as well as substrated phosphorylated by PLKs after recruitment via these phosphorylated PBMs would be interesting next steps. That IRAK phosphorylation may critically regulate TLR post-receptor signaling at the level of the Myddosome complex 6,49 was recently shown by our groups for serine 8 in IRAK4 22 . In depth studies of the novel IRAK phospho-and PBM sites identified here may thus provide further insights into how TLR signaling is regulated and how PLK inhibitors may interfere with the TLR arm of innate immunity. Elucidating the latter appears mandatory to anticipate the potential impact on innate immunity in patients undergoing PLK inhibitor treatments. Although the number of donors analyzed for the inhibitor study was very limited and needs to be expanded (ideally to healthy donors and cancer patients) before drawing more generally applicable conclusions, our results suggest that suppression of TLR signaling could be an unwanted side-effect for the use of PLK inhibitors in humans, they at the same time open up the possibility that PLK inhibitors may offer therapeutic opportunities under disease conditions where excessive TLR-driven cytokine production is pathophysiological, for example in rheumatoid arthritis, psoriasis or lung inflammation Further investigations in experimental in vivo models or monitoring the effects on TLR signaling in clinical studies are clearly warranted.

IRAK2-HA expression and purification.
Human IRAK2 with StrepHA tag 50,51 was expressed from HEK 293 FlipIn TRex as outlined in supplemental methods. In brief, IRAK2-StrepHA-containing lysates were loaded onto a Strep-tactin Sepharose (IBA) column, washed 3 times and eluted with Buffer E (100 mM Tris, pH 8.0; 150 mM NaCl, 1 mM EDTA, 2.5 mM des-thiobiotin). Elution fractions were checked on silver stained gel for protein yield and purity (verified by SDS-PAGE followed by standard silver staining) and pooled for MS/MS. Mass spectrometry analysis of IRAK2. Protein samples were dissolved in denaturation buffer (DB), reduced and alkylated before LysC (Waco) digestion. Phospho-peptides were enriched using TiO 2 beads, subjected to liquid chromatography on an EasyLC nano-HPLC (Proxeon Biosystems) with a nano-HPLC column with C18 spheres (Dr. Maisch) and MS/MS analysis performed on a LTQ-Orbitrap XL mass spectrometer (Thermo Fisher Scientific). Further details are provided in Supplemental Methods. IRAK4 expression and purification. Human IRAK4 was cloned into the pETG30 vector and expressed in BL21 Codon Plus cells as previously described 22,49 . Briefly, IRAK4 was expressed as a GST fusion protein and Prescission protease was used to cleave it from its fusion partner. It was thereafter purified by both ion exchange and size exclusion chromatography.

Dimethyl-labeling of THP-1 cells and global phosho-proteome mass spectrometry analysis.
THP-1 cells (Invivogen) were primed with PMA (300 ng/mL, InvivoGen) overnight and then stimulated with PBS or 5 µM Pam2 for 30 minutes. Dimethyl-labeling of equal amounts of lysate, sample workup, MS acquisition, peak annotation and database searches was done as described in Supplemental Methods. Data were deposited in the PRIDE database (identifier PXD007542).