The PH-BEACH-WD40 (PBW) protein family members play a role in coordinating receptor signaling and intracellular vesicle trafficking. LPS-Responsive-Beige-like Anchor (LRBA) is a PBW protein whose immune function remains elusive. Here we show that LRBA-null mice are viable, but exhibit compromised rejection of allogeneic, xenogeneic and missing self bone-marrow grafts. Further, we demonstrate that LRBA-null Natural Killer (NK) cells exhibit impaired signaling by the key NK activating receptors, NKp46 and NKG2D. However, induction of IFN-γ by cytokines remains intact, indicating LRBA selectively facilitates signals by receptors for ligands expressed on the surface of NK targets. Surprisingly, LRBA limits immunoregulatory cell numbers in tissues where GvHD is primed or initiated, and consistent with this LRBA-null mice also demonstrate resistance to lethal GvHD. These findings demonstrate that LRBA is redundant for host longevity while being essential for both host and donor-mediated immune responses and thus represents a unique and novel molecular target in transplant immunology.
Via a gene-trap approach we identified several novel LPS-responsive genes including the 7a65 gene-trap that harbored a lacZ gene-trap integration into a gene we subsequently cloned and designated LPS-Responsive-Beige-like Anchor (LRBA)1,2. The longest isoform, LRBA-α is a 2,856aa protein that contains a ConA-like/lectin domain (ConA), Armadillo/β-catenin-like repeats (ARM), PKA/C-binding motifs (AKAP), a conserved Domain of Unknown Function (DUF), Pleckstrin Homology (PH) domain, beige and Chediak-Higashi syndrome (BEACH) domain and a series of WD40 repeats at the COOH terminus (Figure S1A)2. In addition, we identified two other murine isoforms, LRBA-β and -γ, those possess unique amino acid stretches at their COOH termini, but also lack all five COOH terminal WD repeats (LRBA-γ) or the two most terminal repeats (LRBA-β)2. The latter is significant because omission of these WD40 repeats may alter the capacity of these shorter isoforms to partner with proteins recognized by these structures. Intriguingly, the LRBA-α, -β, and -γ isoforms are generated by alternative splicing and RT-PCR analysis indicates this regulation results in differential expression of the three isoforms across different tissues and even developmentally within a single cell lineage2. The human and murine LRBA proteins show 90% sequence homology2. LRBA is a member of highly conserved PH-BEACH-WD40 (PBW) protein family3,4. The PBW protein family harbors domains that have capacity to associate with cell membranes (PH, BEACH domains), glycoproteins (ConA-like lectin domain), but also protein-protein interaction domains (WD40 repeats, AKAP motif, ARM domain) and are predicted to serve a scaffolding function uniquely equipped to coordinate vesicle trafficking to sites of receptor signaling at the plasma membrane2,4,5.
LRBA is expressed ubiquitously in normal tissues, but its expression is increased in malignancy, particularly in breast cancer6,7. In immune cells LRBA is found in all membrane compartments associated with receptor signaling including the plasma membrane, golgi complex, clathrin-coated pits and trans-endocytic vesicles2. Based on its domain structure and subcellular localization, we proposed that LRBA coordinates signaling of immune receptors to promote effector function and thus plays a crucial role in immune regulation2. Consistent with this, several recently identified individuals with homozygous or compound heterozygous mutations in LRBA that result in LRBA protein deficiency suffer from immune dysregulation and manifest a spectrum of clinical complications including common variable immune deficiency (CVID), recurrent infections and autoimmunity that also includes inflammatory bowel disease (IBD)8,9,10,11. Further, recently in T-cells LRBA has been shown to regulate CTLA4 turnover hence, modulating CTLA4 mediated immune signaling12. These observations indeed thus support a crucial role of LRBA in immune regulation. However, our understanding of the effector functions regulated by LRBA and how LRBA regulates these immune cell effector functions is still very limited and remains to be studied.
Here, we report the first LRBA-null mouse model. We report that LRBA-null mice show normal life span but exhibit compromised rejection of allogeneic, xenogeneic and missing self bone-marrow (BM) grafts as well resistance to acute graft vs host disease (GvHD). NK cell analysis revealed that NK cells from these mice show defective NK cell activating receptor signaling. Further, LRBA regulates MDSC and Treg numbers in tissues where GvHD is primed. Thus our findings demonstrate a pivotal role of LRBA in NK effector functions and transplant immunology.
LRBA Deficiency Compromises Allogeneic, Minor Histocompatibility Antigen (miHAg) Mismatched, Missing Self and Xenogeneic BM Graft Rejection
In order to assess a possible role for LRBA in cellular immunity, we generated LRBA-null mice (Null) by using embryonic stem (ES) cells where the LRBA gene is inactivated via gene-trap integration into the intron between exons 2 and 3 (Figure S1B). LRBA is abundantly expressed in kidney and brain2 and thus RNA from these tissues was used for Northern blot analysis to confirm that LRBA-null mice lack expression of LRBA mRNA (Figure S1C). Homozygous LRBA-null mice on a 129 Sv background had a normal and healthful lifespan that does not differ significantly from 129 Sv wild-type mice (WT) and heterozygous littermates (LRBA+/−) (Figure S1D). Consistent with their normal lifespan, full necropsy and careful histopathology analysis of all major organs performed on multiple LRBA-null mice did not reveal any significant abnormalities or pathologies (Figure S2). This included the gastrointestinal tract where IBD of various clinical types was reported in all humans homozygous for inactivating LRBA mutations8,9,10,11.
To provide an initial assessment of LRBA’s importance in cellular immunity, we compared the ability of LRBA-null mice on a 129Sv (H2b, Ly5.2+) background to acutely reject BM grafts from MHC-I mismatched (H2d) BALB/C donors. To accomplish this, allogeneic BALB/C BM cells were mixed with syngeneic 129Sv BM cells at 1:1 ratio and injected into lethally-irradiated LRBA-null or WT 129Sv hosts. 7 days later mice were bled and the presence of allogeneic donor cells was analyzed by flow cytometry (Fig. 1A). We observed a significantly greater frequency of allogeneic donor cells in LRBA-null hosts relative to WT hosts (Fig. 1A) suggesting that acute rejection of MHC-I unmatched BM is compromised in LRBA-null hosts. We then analyzed BM graft rejection in the context of extensive miHAg mismatch between donor and host. B6.Ly5.1 (H2b, Ly5.1+) BM cells were mixed with syngeneic BM cells at 1:1 ratio and injected into LRBA-null or WT hosts (Fig. 1B). Thirty days post-transplant splenocytes from WT and LRBA-null mice were analyzed for the presence of donor cells. We observed significantly increased frequency of miHAg mismatched (B6.Ly5.1) donor cells in LRBA-null hosts as compared to WT (Fig. 1B). These findings implicate LRBA as being essential for efficient rejection of MHC-I mismatched donor BM stem/progenitors, a cellular immune function primarily mediated by NK cells. However, diminished rejection of miHAg mismatched grafts indicates the residual T-cell immune barrier in lethally irradiated hosts may also be impaired by LRBA-deficiency, and thus LRBA could also contribute to cytotoxic T-cell function. Although NK cells can also contribute to rejection of miHAg mismatched BM grafts, due to allelic variation in mitochondrial antigens13. Thus, enhanced miHAg engraftment may also reflect NK dysfunction in LRBA-null hosts.
As shown by Karre and colleagues for tumor cells14 and subsequently by Bix et al. for β2m−/− BM grafts15, there is a unique immune role for NK cells in the killing and rejection of missing self tumor cells and BM grafts that lack surface expression of MHC-I. To further confirm that LRBA is required for NK function in vivo, we challenged LRBA-null and WT hosts with MHC-I deficient donor BM cells from TAP2−/−β2m−/− hosts. As with allogeneic donor cells, we observed significantly enhanced acute engraftment of CFSE-labeled missing self TAP2−/−β2m−/− cells (Fig. 1C). As NK cells play a unique role in rejection of missing self grafts these findings unequivocally implicate LRBA in the in-vivo cytotoxic function of NK cells. Improved engraftment of missing self BM cells in LRBA-null hosts suggested that a xenogeneic graft might also be rejected to a lesser degree by LRBA-null hosts. To test this possibility we challenged LRBA-null and WT hosts with human BM cells and assessed acute engraftment the next day. As with missing self grafts, we also observed significantly improved human cell engraftment in LRBA-null hosts as compared to WT, when hosts were conditioned prior to transplant with myeloablative radiation doses (Fig. 1D).
LRBA is Required for Efficient Signaling by Key NK Activating Receptors
To provide mechanistic insights into the NK cell functional deficit identified, we initially assessed NK cell numbers and terminal maturation by CD11b and CD27 staining16. This analysis revealed that NK cells are present at normal numbers in LRBA-null mice and exhibit normal maturation (Figure S3A,B). As NKG2D has been implicated in NK mediated rejection of allogeneic BM grafts17, while NKp46 has been shown to be necessary for NK responses to influenza and certain tumor types18,19, we then examined the expression and signaling capacity of these two key NK activating receptors. Flow cytometric analysis showed that both NKp46 and NKG2D are expressed normally on peripheral NK cells in LRBA-null mice (Figure S3C). Also, LRBA-null mice had unchanged T-cell and B-cell frequency compared to WT mice (Figure S4A–D). We then examined the signaling capacity of these two NK activating receptors by assessing their ability to induce phosphorylation of two key signaling molecules, AKT and ERK1/2 MAPK20,21, and IFN-γ expression. When MACS purified, IL-2 expanded NK cells from WT and LRBA-null mice were stimulated with plate bound agonistic anti-NKG2D and anti-NKp46 antibodies, we observed impaired ERK1/2 and AKT phosphorylation in LRBA-null NK cells compared to WT suggesting signaling defects in LRBA-null NK cells (Fig. 2). We also observed that the engagement of either NKp46 or NKG2D was found to induce IFN-γ expression in a significantly lower proportion of LRBA-null splenic NK cells compared to WT (Fig. 3A). IFN-γ, is a major NK effector cytokine, and ability to induce IFN-γ is widely utilized to test the functional competency of NK cells22,23,24. Inability to induce AKT and ERK1/2 MAPK phosphorylation, and IFN-γ suggests that signaling of both NKp46 and NKG2D is impaired in the LRBA-null NK cells. In order to determine whether LRBA-null NK cells are broadly disabled for induction of IFN-γ we also assessed whether co-stimulation with IL-12 and IL-18 is able to induce IFN-γ in these cells. Multiple independent experiments showed that IFN-γ induction in LRBA-null NK cells was intact following co-stimulation with this cytokine pair (Fig. 3B) that can potently activate NK effector functions independent of activating receptor engagement25. Thus, LRBA-null NK cells are disabled for induction of effector responses triggered by receptors like NKG2D and NKp46 that recognize surface-elaborated ligands on target cells and not soluble factors that promote their differentiation and effector function.
LRBA is Required for MIP-1α Production and Cytolytic Function of NK Cells
We further examined whether defective NKp46 and NKG2D signaling by LRBA-null NK cells also applied to their ligands when expressed on the surface of target cells - a more physiologically relevant means of receptor engagement than antibody cross linking. We tested this by incubating LRBA-null and WT NK cells with PD1.6 and RMA-Rae1 targets cells that express NKp4619 and NKG2D ligands, respectively, and then analyzed production of macrophage activating factor MIP1α (Fig. 4A) and granzyme B secretion (Fig. 4B). The latter assay provides a measure of the capacity of NKp46 and NKG2D to trigger cytolytic function. We observed significantly diminished MIP1α production and cytolytic responses toward PD1.6 and RMA-Rae1 target cells, confirming that both NKp46 and NKG2D signaling are defective in LRBA-null NK cells, and importantly with bonafide cellular targets expressing their respective ligands. The defective NKp46 and NKG2D signaling that we observe using three independent measures indicates LRBA facilitates signaling downstream of these key NK activating receptors.
LRBA Deficiency Promotes Resistance to GvHD
Host vs. graft (HvG) rejection is only one of two immunological hurdles that must be overcome in order for a host to survive a myeloablative allogeneic BMT procedure. The graft vs. host immune response, that culminates in GvHD, constitutes the second and most formidable barrier to host survival26. As documented above LRBA-null hosts have a compromised HvG barrier and thus we considered the possibility that they might also prime a poor GvH response that lead to lethal GvHD. Consistent with this possibility, we find that two major immunoregulatory cells, MDSC and Treg cells, that are known to limit GvHD27,28,29,30,31, are increased in LRBA-null hosts at immune locations where GvHD is initiated. We find that the frequency of MDSC (Mac1+ Gr1+) is significantly increased in both the spleen (Fig. 5A) and mesenteric lymph node (MLN) (Fig. 5B) of LRBA-null mice, while Treg cells, including both native (nTreg) and induced Treg (iTreg) populations are significantly increased in the small intestine of LRBA-null hosts (Fig. 5C). Because of the increased numbers of both immunoregulatory cell types, we then assessed the capacity of LRBA-null splenocytes to prime donor allogeneic T-cell responses in a one-way mixed lymphocyte reaction (MLR) assay. Consistent with the increased numbers of MDSC in LRBA-null spleen we observed that LRBA-null stimulators prime allogeneic T-cell proliferation poorly as compared to WT stimulators (Fig. 5D). The one-way MLR is generally considered an in-vitro surrogate for GvHD; however, it may only be relevant to donor T-cell responses with cells from tissues used in the assay. Thus, we performed a lethal GvHD challenge in LRBA-null hosts to determine if suppression of donor T-cell responses by LRBA host tissues occurs in vivo as measured by host survival. Using a standard lethal acute GvHD BMT model32, we find that LRBA-null hosts exhibit enhanced survival in this setting (Fig. 5E). Thus, LRBA deficiency also abrogates donor allogeneic immune responses that culminate in lethal acute GvHD during MHC-I unmatched BMT.
Recent reports identifying immune dysfunction in LRBA-deficient patients suggest a critical role of LRBA in immune homeostasis. The induction of LRBA expression by mitogen and its ability to traffic to the plasma membrane or sites of receptor-mediated endocytosis suggested LRBA might have a role in receptor signaling by immune effector cells2. However, our understanding of the effector functions regulated by LRBA and how LRBA regulates these immune cell effector functions is very limited and remains to be studied. Here, we studied the role of LRBA in regulating NK effector functions and BM transplantation. We show that LRBA is pivotal for NK cell mediated rejection of allogeneic, missing self and xenogeneic hematopoietic grafts and may also be required for T-cell responses to miHAg mismatched grafts. However, NK cells can also distinguish and reject miHAg mismatched cells based on variation in mitochondrial DNA content via MyD88 signaling13. Thus, it is possible that LRBA could also facilitate MyD88-mediated NK rejection of miHAg mismatched BM grafts. In addition, LRBA is also required for homeostatic control of MDSC and Treg cells and consistent with this LRBA-null hosts show significant resistance to acute GvHD following MHC-I unmatched BMT. Inability to reject allogeneic BM grafts and resistance to acute GvHD observed in LRBA-null mice suggests the possibility that the recently identified LRBA-deficient patients are strong candidates to benefit from allogeneic BMT8,9,10,11.
Our analysis indicates LRBA selectively facilitates receptor signals from major NK activating receptors like NKp46 and NKG2D that interact with ligands expressed on the surface of virally infected, stressed or malignant targets. However, LRBA does not appear to be required for signaling by soluble inducers of NK effector function like IL12 and IL18. This distinction may provide insights into LRBA’s role in promoting NK effector functions. PBW proteins possess domains that can associate with inositol phospholipid species33,34, vesicular membranes2 and plasma membrane sites involved in receptor signaling2. Like other members of the PBW protein family, LRBA possesses domains that could enable its recruitment to the plasma membrane at sites near to the cellular receptors, and thus can coordinate recruitment of vesicles containing effector cytokines or cytolytic proteins to enable efficient secretion and targeting of these cargoes toward their targets. Cytoplasmic granules within CTL and NK cells release Granzyme B that induce apoptosis within virus-infected cells or tumor cells. As predicted, LRBA-null NK cells stimulated with either PD1.6 or RMA-Rae1 exhibited greatly impaired secretion of both MIP-1α and Granzyme B and also exhibited impaired phosphorylation of AKT and ERK1/2 MAPK as compared with WT control suggesting that LRBA can also facilitate the PI3K-RacI-PAK-MEK-ERK pathway that promotes trafficking of lytic granules in NK cells toward targets cells20,35. LRBA thus may be coordinating receptor signaling events with effector functions in NK cells by regulating efficient trafficking of cytolytic granules or cytokines downstream of activating receptors such as NKp46 and NKG2D. In this regard it is intriguing that Neurobeachin, the PBW paralog with the highest degree of homology to LRBA, is required for synapse function in neuronal cells33,34,36. Perhaps LRBA has a comparable role in the synapse that NK cells form with their targets. This could account for the fact that LRBA deficiency does not impair induction of NK effector function by soluble activators like IL12 and 18, but is critical for responses to ligands presented on the surface of target cells. Also, NK cell IFN-γ is known to have direct and indirect effects on other immune cells like T-cells and DCs37. IFN-γ can induce maturation of DC leading to IL12 production and increased co-stimulation. DC maturation in turns promotes enhanced T-cell responses37. Low IFN-γ production by Null NK cells thus means there could be reduced or compromised DC activation and priming of T cells. That might also explain defective priming of allogeneic T-cells by LRBA-null cells in our MLR and GvHD assays. Further, defective NKG2D and NKp46 signaling observed in LRBA-null NK cells caution us that LRBA-deficient patients may be highly susceptible to tumors and viral infections as these two receptors are crucial for anti-tumor and anti viral immune responses17,18,19. Indeed, in a recent paper Gamez-Diaz et al., reported that in a cohort of 22 LRBA-deficient patients viral infections were the most frequent infections and 9/22 patients (41%) suffered from them. Common viral infections were cytomegalovirus, adenovirus, norovirus, and herpes virus. Thus clearly suggesting NK cell defects11.
Contrary to its apparent positive signaling role in promoting NK effector function, LRBA appears to play a role in signals that limit the numbers of MDSC and Treg cells. Intriguingly, the latter role for LRBA is quite tissue specific as n and iTreg increases were only observed in the small intestine of LRBA-null hosts. Interestingly, GvHD is thought to be initiated in the gut where myeloablative strategies such as total body irradiation compromise the integrity of the gut epithelium leading to commensal encroachment and consequently an inflammatory milieu that supports efficient priming of donor T-cells that mediate lethal GvHD38. Perhaps increased Treg cell numbers there limit the initiation of GvHD in the LRBA-deficient host with increased MDSC numbers further dampening the spread of GvHD to other tissues by donor T-cells that escape control by Treg cells in the small intestine.
The improved durable engraftment of MHC class I- and miHAg-mismatched BM grafts with reduced incidence and severity of GvHD that we observe in LRBA-deficient mice suggests the possibility that the recently identified LRBA-deficient patients are strong candidates to benefit from allogeneic BMT using related HLA haploidentical or HLA-matched donors8,9,10,11. In this regard, the longevity of LRBA-null mice and the absence of any detectable pathology in non-hematopoietic organs and tissues indicate hematolymphoid reconstitution from allogeneic LRBA-sufficient donors would enable long-term survival in these transplanted patients, as LRBA-deficiency does not have a significant effect on the function and longevity of non-hematopoietic tissues and organs. Indeed recently, a small subset of LRBA-deficient patients were treated with HSCT. Out of 6 patients treated so far 4 patients survived and 2 of the patients died11,39,40,41. One patient died from respiratory failure and the 2nd patient died of thrombotic thrombocytopenic purpura11. However, despite that only a handful of patients being treated the success rate of HSCT is remarkable that clearly underlines the importance of our study. Findings from our study thus clearly support that LRBA-deficient patients are good candidate for receiving a HSCT. However, caution should be applied before extrapolating findings from mouse study to humans as LRBA-deficient patients are progeny of consanguine matings, it’s possible that they are homozygous for many other alleles that could, in concert with LRBA deficiency, cause the observed immune phenotypes in these individuals. Indeed, a high degree of variation in the occurrence and severity of spectrum of disease phenotypes in LRBA-deficient patients strongly suggests that LRBA-deficiency is modified by alleles at other loci to promote disease in these patients. However, that is not the case with the LRBA-null mice on a defined genetic background. Further, in case of human subjects results could vary from individual to individual, as there could be many factors that can effect the outcome of a HSCT that includes:- the disease progression stage (early vs late) at which HSCT is performed, the conditioning regiment used for lymphodepletion, the donor source, the post-transplant recovery, post-transplantation viral infections (patient 1) and sepsis and GvHD. Thus, risk of allogeneic HSCT should be weighed against the clinical presentation in each individual case. Further, our finding that xenogeneic human BM cells are rejected less efficiently in LRBA-null hosts may have practical implications for the development of novel immunodeficient mouse models of human immunity and hematopoiesis where LRBA mutation could be combined to other immune deficient mutations. Collectively, our study suggests that LRBA represents truly unique molecular target in transplant immunology, as it plays a pivotal role in both HvG and GvH immune reactions while not being required for host viability.
B6.Ly5.1 (H2b Ly5.1+) or BALB/c (H2d) were purchased from Jackson and 129Sv (H2b Ly5.2+) or TAP2−/−β2m−/− mice were purchased from Taconic. All mice were used at the age of 8–12 weeks. LRBA−/− mice were derived via blastocyst injection of embryonic stem cells harboring a gene-trap retrovirus42 whose integration in the LRBA gene inactivates its expression by introduction of an artificial exon that terminates endogenous LRBA transcription and splicing to downstream exons. Southern blotting was used to identify murine progeny with significant transmission of the LRBA gene-trap integration and these chimeric mice were then crossed to 129Sv partners to obtain mice that have germline transmission of the LRBA mutant allele on a pure 129Sv genetic background. These LRBA+/− progeny were then intercrossed to obtain LRBA-null homozygous mice with confirmation of the null homozygous genotype by a multiplex PCR. Northern blotting of kidneys and brains, two tissues that have abundant LRBA expression, confirmed that LRBA-null mice lack detectable mRNA expression from the LRBA locus. All animal experiments were approved by Institutional Animal Care and Use Committee (IACUC) of SUNY Upstate Medical University and performed in accordance with approved guidelines.
Flow cytometry analysis
Antibodies were purchased from BD Biosciences (San Jose, CA) or eBioscience (San Diego, CA). Samples were Fc blocked with anti-CD16/CD32 and then stained with the indicated antibodies and acquired on LSRII or Fortessa. Various antibodies used for staining are: CD49b-PE (DX5), CD3-PerCPCy5.5 (145-2C11), CD335-FITC (NKp46, 29A1.4), CD314-PE Cy-7 (NKG2D, CX5), H2d-FITC (34-2-12) and H2b-PE (AF6-88.5) or H2b-PECy7, CD45.1-PE (A20) and CD45.2-FITC (104). For MDSC analysis CD11b-APC-Cy7(M1/70) and Gr1(RB6-8C5)-PE antibodies were used. For Treg cell analysis small intestine lamina propria T cells were isolated as described previously43 and stained with CD3 PECy7 (145-2C11), CD4 FITC (RM4-5), CD25 APC (PC61.5) and Foxp3 PE (FJK-16s) antibodies.
For licensing assays, mice were injected i.p. with 70 μg of Poly IC on day –1. Spleens were harvested next day, RBC lysed and resuspended in RPMI 1640 supplemented with 10% FBS, 1% penicillin-streptomycin, 1% L-glutamine, 1% sodium pyruvate, and 1% nonessential amino acids. 4–6 million splenocytes were incubated with plate bound anti-NKG2D (A10) or anti-NKp46 (29A1.4) in 6-well plates for 5–6 h at 37 °C in the presence of GolgiPlug. The cells were harvested, and stained for CD49b-PE(DX5) and TCR-FITC (H57-597) and then permeabilized and fixed using the eBioscience Fixation/Permeabilization kit and stained with anti-IFN-γ-APC (XMG1.2). To stimulate NK cells using IL12/18, 5–6 million splenocytes were incubated in 6 well plates overnight in presence of 20ng/well IL12 and 100ng/well IL18. The next morning cells were incubated for 3–4 hr at 37 °C in the presence of GolgiPlug and harvested for flow analysis.
LRBA-null or WT NK cells were added to a 96-well granzyme B ELISpot plate at a concentration of 5 × 104 cells/well. 1 × 104 PD1.6 or RMA-Rae1+ cells were then added to the well as a stimulus for NK cells and microplate was incubated for 20 hr at 37□C in a CO2 incubator. Cells were removed and the supernatant was harvested to perform MIP-1α ELISA assay. ELISPOT assay was performed according to the manufacturer’s protocol (EL1865; R&D Systems). The number of spots corresponding to Granzyme B-secreting cells was determined using an automatic CTL ELISPOT Reader (Shaker Heights, OH). The number of background spots in wells without target cells was subtracted from the wells containing target cells and NK cells.
Assessment of MIP-1α levels by ELISA assay
MIP-1α ELISA kit (MMA00) was purchased from R&D Systems Inc. (Minneapolis, MN) and MIP-1α ELISA was performed according to the manufacturer’s protocol.
Dye labeling and flow cytometry based detection of donor cells in vivo
For dye labeling BM cells were labelled with CFSE or DDAO-SE (Invitrogen, Carlsbad, CA) at a concentration of 5μM in PBS at 37 °C for 15 minutes. For missing self acute engraftment, 1 × 107 TAP2−/−β2m−/− BM cells stained with CFSE and 1 × 107 129Sv (H2b+) BM cells stained with DDAO were mixed at 1:1 ratio and injected intravenously into lethally irradiated (1100Rad, split dose 600 + 500) WT or LRBA-null hosts. After 18hr PBMC from these mice were analyzed by flow cytometry for CFSE+ and DDAO+ cells. For 7 days acute engraftment, 2 × 106 Balb/c (H2d) BM cells and 2 × 106 syngeneic 129Sv (H2b) BM cells (4 × 106 BM cells total/host) were infused intravenously via retro-orbital injection into lethally irradiated WT or LRBA-null hosts. To assess engraftment, peripheral blood mononuclear cells were harvested 7 days after BMT and stained for H2d and H2b and analyzed by flow cytometry. For minor histocompatibility antigen (miHAg) mismatched BM graft rejection splenocyte from recipients were harvested one month following BMT and analyzed. For xenogeneic transplantation human BM from healthy donors was purchased from Lonza (Allendale, NJ). CFSE labeled 5 × 106 human BM cells were intravenously injected into WT or LRBA-null hosts that received either 550 or 1100Rads. After 18 hours the recipients were bled and analyzed by flow cytometry.
For Immunoblot analysis MACS purified NK cells were expanded in presence of recombinant human IL2 for 7 days. Cells were IL2 starved overnight and stimulated with plate bound NKG2D (A10) and NKp46 antibodies for 15 minutes. After 15 minutes cells were lysed in cell lysis buffer (Cell Signaling Technology) and equal amount of protein was run on SDS-PAGE. Proteins were transferred to nitrocellulose membrane and probed with p-ERK1/2, ERK1/2, p-AKT (Ser473) and AKT antibodies, all from Cell Signaling Technology except AKT which was from Santa Cruz. Immuno-reactive bands were visualized using ECL reagent (Thermo Scientific).
129Sv WT and LRBA-null mice were lethally irradiated followed by infusion of 107 CD3-depleted BALB/c bone marrow cells plus 2 × 106 splenic MACS purified T-cells via tail vein injection. Mice were monitored for survival and difference in animal survival were analyzed using a Kaplan-Meier log-rank test.
Mixed Lymphocyte Reaction (MLR)
RBC lysed splenocytes from LRBA-null and WT mice were irradiated at 2000 rad (Stimulators) and co-cultured with CFSE labeled RBC lysed BALB/c splenocytes (responders) at a ratio of 2:1 in a one way MLR assay28,44. On day 4th proliferation of responder T cells (H2d+CD3+) was assessed by flow cytometric analysis of CFSE dilution44.
Data were analyzed for statistical significance using Prism (GraphPad, San Diego, CA). Students t-test was used to calculate the significance between groups. Differences in animal survival (Kaplan Meier curves) were analysed by log-rank test. Results were considered significant if p value is ≤0.05.
How to cite this article: Park, M. Y. et al. LRBA is Essential for Allogeneic Responses in Bone Marrow Transplantation. Sci. Rep. 6, 36568; doi: 10.1038/srep36568 (2016).
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We thank Sandra Fernandes for assistance with establishing the GvHD model used in this study. This work was supported in part by grants from the NIH (RO1 HL72523, R01 HL085580, R01 HL107127) and the Paige Arnold Butterfly Run. WGK is the Murphy Family Professor of Children’s Oncology Research, an Empire Scholar of the State University of NY and a Senior Scholar of the Crohn’s and Colitis Foundation of America.
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