Functional requirements for inhibitory signal transmission by the immunomodulatory receptor CD300a
© DeBell et al.; licensee BioMed Central Ltd. 2012
Received: 9 November 2011
Accepted: 26 April 2012
Published: 26 April 2012
Activation signals can be negatively regulated by cell surface receptors bearing immunoreceptor tyrosine-based inhibitory motifs (ITIMs). CD300a, an ITIM bearing type I transmembrane protein, is expressed on many hematopoietic cells, including subsets of lymphocytes.
We have taken two approaches to further define the mechanism by which CD300a acts as an inhibitor of immune cell receptor signaling. First, we have expressed in Jurkat T cells a chimeric receptor consisting of the extracellular domains of killer-cell immunoglobulin-like receptor (KIR)2DL2 fused to the transmembrane and cytoplasmic segments of CD300a (KIR-CD300a) to explore surrogate ligand-stimulated inhibition of superantigen stimulated T cell receptor (TCR) mediated cell signaling. We found that intact CD300a ITIMs were essential for inhibition and that the tyrosine phosphorylation of these ITIMs required the src tyrosine kinase Lck. Tyrosine phosphorylation of the CD300a ITIMs created docking sites for both src homology 2 domain containing protein tyrosine phosphatase (SHP)-1 and SHP-2. Suppression of SHP-1 and SHP-2 expression in KIR-CD300a Jurkat T cells with siRNA and the use of DT40 chicken B cell lines expressing CD300a and deficient in several phosphatases revealed that SHP-1, but not SHP-2 or the src homology 2 domain containing inositol 5’ phosphatase SHIP, was utilized by CD300a for its inhibitory activity.
These studies provide new insights into the function of CD300a in tuning T and B cell responses.
An appropriate immune response requires a fine balance between a multitude of activating and inhibitory signals and the loss of the ability to limit positive signaling can result in autoreactivity and excessive inflammation [1, 2]. A diverse array of inhibitory receptors participates in the negative control of the immune response. A characteristic of many of these receptors is a consensus amino acid sequence in their cytoplasmic tail, i.e. the immunoreceptor tyrosine-based inhibitory motif (ITIM) [3–8]. Ligand interaction with these receptors results in ITIM tyrosine phosphorylation, usually by a src family kinase, providing sites for binding proteins via their src-homology 2 (SH2) domains [9–14]. Proteins containing consensus sequences for interaction with phosphorylated ITIMs include the SH2 domain-containing tyrosine phosphatase (SHP)-1, SHP-2, and the SH2 domain-containing inositol 5’-phosphatase (SHIP) [10, 13–16]. The recruitment of phosphatases to the phosphorylated ITIMs results in their activation and the subsequent dephosphorylation of their substrates, leading to the down-regulation of activation signals [9–14]. Although several targets of these phosphatases have been proposed, the specific pathways and mechanisms by which each phosphatase participates in the signaling cascade downstream from the inhibitory receptors remain incompletely understood [17–19].
CD300a is one of the seven members of the CD300 family of leukocyte surface receptors that are encoded by genes clustered in human chromosome 17q25 . Like the other members of the CD300 family, CD300a is a type I transmembrane protein, with a single IgV-like extracellular region and three classical and one non-classical ITIMs in its cytoplasmic tail . The CD300a gene has undergone a very significant positive selection, suggesting an essential requirement for the host to maintain its function throughout evolution [21, 22]. CD300a is expressed on cells of both the myeloid and lymphoid lineages . The clinical relevance of this receptor is demonstrated in reports showing the association of a non-synonymous polymorphism within the Ig-V domain with the development of psoriasis , the implication in the development of Alzheimer’s disease by genome wide association studies , the down-regulation of CD300a expression on B cells from HIV-1 infected patients , and the proposed use of CD300a as a biomarker that can differentiate ulcerative colitis from Crohn’s disease and non-inflammatory diarrhea  and for the detection of minimal residual disease in acute lymphoblastic leukemia .
In vitro studies have shown that CD300a ligation can inhibit NK cell mediated cytotoxicity [28, 29], FcϵRI mediated activation of mast cells , FcγRIIa mediated reactive oxygen species production and Ca2+ flux in neutrophils  and eosinophils responses to eotaxin, GM-CSF and IL-5 . Additionally, it has been shown to inhibit both B cell receptor (BCR) and T cell receptor (TCR) mediated Ca2+ mobilization and NFAT mediated transcriptional activity [25, 33]. Furthermore, in vivo studies in mice have shown that CD300a is able to reverse remodeling and airway inflammation in a model of experimental asthma , to abrogate IgE mediated allergic reactions  and to inhibit stem cell factor (SCF) induced anaphylaxis . Various mechanisms of the CD300a mediated inhibitory signaling have been proposed. Several publications have shown that phosphorylated CD300a is able to recruit different phosphatases depending on the examined cell type, although genetic evidences for the direct involvement of any phosphatase in the delivery of CD300a mediated inhibitory signal is lacking. For example, treatment of human NK cells with pervanadate led to tyrosine phosphorylation of CD300a and its association with both SHP-1 and SHP-2 , while in eosinophils cross-linking of the receptor with monoclonal antibodies (mAb) recruited SHP-1 but not SHP-2 . In mast cells, after pervanadate treatment, SHP-1 and SHIP, but not SHP-2 co-precipitated with CD300a, while upon mAb driven cross-linking, SHIP, but not SHP-1 associated with CD300a . Also in mast cells, precipitation of CD300a from cells treated with an anti-Kit-CD300a bispecific antibody induced its tyrosine phosphorylation and the recruitment of SHIP, but not SHP-1 .
In T and B lymphocytes the expression of CD300a is restricted to certain subsets [25, 33, 37, 38]. Although it has been previously shown that ligation of CD300a with mAb inhibits BCR  and TCR mediated signals , the basis for this inhibition is not known. In this study we investigate the structural and functional requirements for CD300a mediated inhibitory signaling in B and T cells. Importantly, we establish a physiologically relevant model in which we explore ligand driven functions of CD300a. To accomplish this, a KIR-CD300a chimera was expressed in Jurkat T cells. Mixing these cells with MHC class I matched antigen presenting cells that were loaded with superantigen allowed us to determine the importance of the CD300a ITIMs, the means by which they are phosphorylated and the phosphatases that subsequently associate with them. Further studies, using DT40 B cell lines and siRNA mediated knock down of SHP-1 and SHP-2 in Jurkat T cells, were performed to discriminate among signaling intermediates utilized by CD300a.
Intact ITIM motifs are required for CD300a mediated inhibitory signal
The intracellular tail of CD300a inhibits superantigen mediated activation of T cells
To further prove that the intracellular tail of CD300a is responsible for the inhibitory signal we performed additional experiments measuring NFAT transcriptional activity. We transiently transfected the E6.1 Jurkat T cell line and the KIR-CD300a WT and KIR-CD300a 4F expressing Jurkat T cells with a plasmid encoding the luciferase reporter gene under the control of a NFAT dependent promoter. Cells were stimulated through the TCR with SED presented by 721.221, 721.221-Cw3 and 721.221-Cw6 cells. The MHC class I molecule HLA-Cw6 is not a ligand for KIR2DL2 . Results in Figure 3D showed that there was a decrease in the NFAT transcriptional activity only when KIR-CD300a WT Jurkat T cells were stimulated with SED solely presented by 721.221-Cw3 cells, and not 721.221 or 721.221-Cw6 cells. These results confirmed that the inhibition of superantigen mediated activation of Jurkat T cells required both the specific interaction between KIR2DL2 with its ligand, HLA-Cw3, and an intact CD300a intracellular tail.
The src kinase lck is responsible for the tyrosine phosphorylation of CD300a on Jurkat T cells
It has been previously described that the src kinase Lck is required for KIR tyrosine phosphorylation . In our experimental system, in order to identify the kinase responsible for phosphorylation of CD300a ITIMs, the E6.1 Jurkat T cell line and the Jurkat T cell lines deficient in Lck or ZAP-70 were transiently transfected with a plasmid encoding KIR-CD300a WT. These cells were mixed with 721.221-Cw3 or 721.221-Cw6 cells and tyrosine phosphorylation was assessed in KIR2DL2 immunoprecipitates (Figure 4B). Co-incubation of 721.221-Cw3 cells with either the E6.1 Jurkat T cell line or the ZAP-70 deficient cells led to tyrosine phosphorylation of KIR-C300a, indicating that ZAP-70 is not necessary for tyrosine phosphorylation of the intracellular tail of CD300a. However, when Jurkat T cells deficient in Lck were incubated with 721.221-Cw3, tyrosine phosphorylation of KIR-CD300a was not observed in any of the immunoprecipitates. As expected, co-incubation of any Jurkat T cell lines with 721.221-Cw6 cells did not stimulate tyrosine phosphorylation of KIR-CD300a WT. Together, these results show that ligand-receptor interaction leads to tyrosine phosphorylation of the CD300a ITIMs in the absence of an activation signal, and that the src kinase Lck is responsible for tyrosine phosphorylation of the CD300a ITIM motifs in Jurkat T cells.
Both SHP-1 and SHP-2 bind to CD300a ITIM, but only SHP-1 is necessary for CD300a mediated inhibition
In this report, we provide evidence that the primary function of CD300a in T and B cells is to limit antigen receptor mediated positive signaling and that the phosphatase SHP-1 is required for this function. Coligation of the BCR and CD300a with mAb reduced BCR stimulated Ca2+ mobilization and NFAT transcriptional activity. In the absence of SHP-1, but not SHP-2 or SHIP, CD300a mediated inhibition was significantly reduced. Additionally, we show that superantigen induced activation was inhibited when Jurkat T cells expressing the chimeric receptor KIR-CD300a were mixed with antigen presenting cells expressing the KIR2DL2 ligand HLA-Cw3. The interaction of KIR-CD300a with its ligand led to the tyrosine phosphorylation of CD300a ITIM motifs. This phosphorylation required the src kinase Lck, and provided docking sites for the binding of the phosphatases SHP-1 and SHP-2. These early events were followed by the inhibition of superantigen mediated up-regulation of activation markers CD25 and CD69.
The employment of two different models in attempting to understand CD300a inhibitory signal in lymphocytes was very important in our studies. Since DT40 chicken B cells do not express CD300a, the usage of these cells and their knockout counterparts allowed us to specifically express both CD300a and phosphatases, wild type and mutants, and to investigate the role of phosphatases in CD300a signaling transmission. In our hands, and with the available anti-CD300a mAb, we were unable to immunoprecipitate CD300a (data not shown). Due to this inability to immunoprecipitate CD300a and, because we also were interested in an experimental system that relies on receptor-ligand interaction, we generated the chimeric receptor KIR-CD300a. Results obtained with similar chimeric receptors have proved useful in gaining information about the role of the ITIMs. For example, by using a chimeric receptor consisting of KIR extracellular domain fused to the FcγRIIb intracellular tail, Gupta et al. demonstrated that the ITIMs in the intracellular tail, and not the extracellular portion, are responsible for the transmission of the inhibitory signal and determined which phosphatase was employed .
For a more comprehensive understanding of CD300a mediated signaling on lymphocytes, mutational analysis of the ITIMs should prove helpful. Lankry et al. have undertaken these studies using the human YTS NK cell line . Their results indicated that all of the ITIMs, including the non-classical 4th ITIM, were important for the inhibitory function of CD300a, with the 3rd ITIM being the most essential. Results obtained in our laboratory in which we mutated tyrosine residues to phenlyalanine instead of to alanine, as described by Lankry et al. , have confirmed that a single mutation of the 3rd ITIM significantly decreased BCR stimulated Ca2+ release and NFAT transcriptional activity (data not shown).
In our KIR-CD300a chimera, the CD300a ITIMs were phosphorylated upon interaction with the KIR ligand without the requirement of superantigen stimulation. This is not surprising, since phosphorylation of KIR ITIMs by Lck also occurs independently of antigen stimulation [9, 42]. However, it is interesting that a single tyrosine kinase, such as Lck, can be utilized for both inhibitory and activating receptors. While the mechanism by which this occurs is still under investigation, findings obtained by Stefanova et al.  may shed some light on this conundrum. In that report, antagonist and agonist peptides, defined by their different binding affinities to the TCR, were used to dissect the seemingly different roles of Lck in T cell homeostasis. The SHP-1 tyrosine phosphatase was a central player in their findings. When T cells were stimulated with a weak binding ligand, Lck phosphorylated SHP-1. Subsequent association of SHP-1 with Lck mediated the recruitment of SHP-1 to the TCR complex where it was proposed that SHP-1 then dephosphorylated Lck at Y394 leading to TCR desensitization. Alternatively, upon interaction with a strong TCR ligand, Erk was rapidly activated and phosphorylated Lck on serine residues (S59). This serine phosphorylation decreased the ability of Lck to bind SHP-1 and therefore the positive signaling proceeded. Here, we have shown that Lck is involved in CD300a phosphorylation. It may be possible that Lck also phosphorylates CD300a bound SHP-1, subsequently aiding in the recruitment of SHP-1 to the TCR complex, leading to the inhibition of positive signaling. Future studies should address this hypothesis.
Our results using SHP-1 and SHP-2 knocked down KIR-CD300a WT Jurkat T cells and specific phosphatase deficient DT40 chicken B cells indicated that SHP-1, but not SHP-2 or SHIP was necessary for CD300a mediated inhibition of BCR and TCR signaling. Although mAb cross-linking induced coimmunoprecipitation of SHIP with CD300a in mast cells , the consensus binding sequences for SHIP are different from that of SHP-1 and SHP-2 and are not present in CD300a. SHIP has no preference for binding to residues N-terminal to the phosphorylated tyrosine (pY) but has a strong preference for Leu at the +2 position. Instead, SHP SH2 domains prefer a hydrophobic residue at the −2 position on the ITIM . All three classical ITIMs present in CD300a have hydrophobic residues at −2 and none of them have Leu at +2 position . Therefore, while the detection of SHIP in a complex with CD300a may indicate a role for SHIP in the control of signaling in mast cells, its direct binding to CD300a ITIM motifs is unlikely. On the other hand, the consensus binding motifs for SHP-1 and SHP-2 are similar  and matched sequences are found in the CD300a intracellular tail . Indeed, both SHP-1 and SHP-2 were detected in immunoprecipitates from ligand stimulated Jurkat T cells expressing the KIR-CD300a chimeric receptor. However, according to previously published results that tested the binding of SHP SH2 domains to pY peptide libraries , it may be that the chances of having both SH2 domains of a single phosphatase bound simultaneously to phosphorylated CD300a intracellular tail are greater with SHP-1. While binding of a single SH2 domain may potentiate phosphatase activity, binding of both domains further increases the activity by several fold .
Further evidence that both SHP-1 and SHP-2 bind to CD300a comes from the SHP-1 and SHP-2 reconstitution experiments. As shown in Figure 6, the expression of either SHP-1 CS or SHP-2 CS reduced the inhibitory function of CD300a. The mutation of the cysteine residue renders the phosphatases catalytically inactive, but they still are able to bind the target ITIM sequences and therefore become dominant negative. In that same line of thought, one could argue that since SHP-2 WT also competes for CD300a ITIM occupancy, it could also function as a dominant negative, and in fact, reconstitution of CD300a expressing DT40 chicken B cells lacking SHP-2 with human SHP-2 WT resulted in a decrease in the CD300a mediated inhibitory ability when compared with non-reconstituted DT40 cells lacking SHP-2 (see Figure 6C). Additional studies designed to address the relative binding affinity of SHP-1 and SHP-2 to phosphorylated CD300a ITIMs and their differential role in signaling should prove interesting.
Taken together, we have demonstrated that CD300a inhibits lymphocyte immune receptor signaling via SHP-1. Although both SHP-1 and SHP-2 are recruited to the phosphorylated ITIMs of CD300a, only the absence of SHP-1 limited the ability of CD300a to inhibit activation signals. SHP-1 has historically been associated with negative signaling while SHP-2 has been associated with positive signals . Beyond similarities in their SH2 domains, the two phosphatases display little sequence homology. SHP-1 but not SHP-2 displays localization signals in particular for lipid rafts while only SHP-2 has proline-rich domains which could recruit SH3 domain containing proteins . However, the specific roles of these regions may play in the function of the two phosphatases remains to be defined. With this in mind, the availability of the different phosphatases to bind the CD300a intracellular tail following receptor ligation will determine the final outcome of the CD300a mediated signaling.
Cells and reagents
The E6.1 Jurkat T cell line, the Jurkat T cell lines deficient in Lck (JCaM1.6)  and ZAP-70 (P116) , the DT40 chicken B cell line , the DT40 mutant cell lines lacking SHP-1, SHP-2 and SHIP [14, 49], and the MHC class I deficient human lymphoblastoid B cell line 721.221 and its clones expressing HLA-Cw3 and -Cw6 [50, 51] were all maintained in RPMI medium containing 7.5% FBS.
To generate stable transfectants, 1 x 107 DT40 chicken B cells or E6.1 Jurkat T cells were transfected with the designated plasmids by electroporation. For DT40 chicken B cells, in addition to the CD300a and phosphatase expressing plasmids, cells were also transfected with 5 μg of the pBABE puro vector . After 48 hours in complete medium, cells were selected with neomycin (Invitrogen) or puromycin (Sigma). Cells were tested for CD300a expression, sorted using a FACS Aria sorter (BD Biosciences) and positive cells were further expanded. Cells transfected with plasmids expressing both CD300a and phosphatases were preselected for CD300a expression, then cloned and tested by Western blot for phosphatase expression. All transfected DT40 chicken B cells and Jurkat T cells expressed similar levels of CD300a and KIR-CD300a, respectively (data not shown).
Antibodies used in this study were obtained from the following vendors: PE-Cy7 anti-CD19 (clone HIB19), Alexa Fluor 488 anti-CD25 (clone BC96), PE anti-CD69 (clone FN50) and isotype control murine IgG1κ were purchased from eBioscience; purified anti-CD158b (clone GL183), PE and purified anti-CD300a (clone E59.126) were purchased from Beckman Coulter; PE anti-CD158b (clone DX27) was purchased from BioLegend; purified anti-chicken IgM (clone M1) was purchased from Southern Biotech; FITC goat anti-mouse IgG F(ab’)2 was purchased from KPL; anti-HA high affinity (clone 3F10) and 3F10-HRP were purchased from Roche-Diagnostics; rabbit anti-mouse IgG was purchased from MP Biomedicals; goat anti-mouse IgG was purchased from Jackson ImmunoResearch Laboratories; anti-phosphotyrosine (clone 4G10), biotinylated 4G10, and anti-SHP-1 antibodies were from Millipore; anti-SHP-2 (clone 79/PTP1D/SHP2) was from BD Biosciences; anti-mouse HRP and anti-rabbit HRP were purchased from GE Healthcare and NeutrAvidin-HRP was from Fisher. SHP-1 specific siRNA duplexes were from Sigma, and non-target (NT) and SHP-2 specific siRNA duplexes were from Dharmacon.
A plasmid encoding human CD300a was previously described . The KIR-CD300a chimeric construct was engineered by fusing the extracellular domain of the KIR2DL2 receptor to the transmembrane and cytoplasmic domains of CD300a tagged with HA (Figure 2). A KIR2DL2 expressing plasmid (a generous gift of Dr. Eric O. Long) was used as a template for the extracellular domain of KIR2DL2. The following primers were used for the PCR reaction: a forward primer 5’ GGGGTACCGCCGCCATGTCGCTCATGGTCG 3’ and a reverse primer 5’ GAAGATCTGTGCAGGTGTCGGGG 3’. A pMACS CD300a-HA plasmid (engineered in our laboratory) was used as a template for the transmembrane and cytoplasmic tail of CD300a tagged with HA. The following primers were used for the PCR reaction: a forward primer 5’ GAAGATCTCTCTGCTCCTCTCCCTGC 3’ and a reverse primer 5’ GCTCTAGATCATTAAGCGTAGTCTGG 3’. The PCR products were purified and digested with the restriction enzymes Kpn I/Bgl II and Bgl II/Xba I, respectively. Digested products were ligated into an empty pcDNA3.1 mammalian expression vector digested with Kpn I and Xba I. Mutagenesis of CD300a and KIR-CD300a expressing plasmids were performed with specific primers using a Quick Change Site-directed mutagenesis kit (Stratagene). DNA sequencing analysis confirmed the sequences of each construct. Plasmids expressing human SHP-1 and SHP-2, wild type (WT) and the catalytically inactive (CS mutation), were a generous gift of Dr. Eric O. Long.
Cell activation, immunoprecipitation and western blot analyses
Jurkat T cells, 5–10 x 106, were prewarmed at 37°C, treated with 0.1 mM sodium orthovanadate and 0.3 mM hydrogen peroxide for 3–5 minutes and then lysed with 50 mM Tris HCl containing 1% NP40 plus protease and phosphatase inhibitors as previously described . In other experiments, Jurkat T cells were mixed with an equal number of the indicated antigen presenting cells (721.221 cells), in the absence or presence of staphylococcal enterotoxin D (SED) (Toxin Technology) at 100 ng/ml while maintained on ice and then centrifuged to promote cell to cell contact. The supernatants were removed and the cell pellets were incubated at 37°C and then, cells were lysed as described above. For immunoprecipitation experiments, cell lysates were precleared with Protein A/G beads (Pierce) for one hour followed by precipitation with Protein A/G beads preloaded with 1.6 μg of anti-KIR2DL2 (clone GL183). Eluted proteins were resolved on gradient gels (Invitrogen), transferred to nitrocellulose and probed with the indicated antibodies.
Flow cytometry experiments
Jurkat T cells, 1 x 106, were mixed with an equal number of 721.221 cells and distributed in wells of a 12 well plate without or with 100 ng/ml SED. After 24 h of culture, the expression of CD25 and CD69 by the Jurkat T cells was assessed by flow cytometry using a FACS Calibur (BD Biosciences). Jurkat T cells were electronically gated by size and forward scatter and by their lack of expression of CD19, a marker expressed by the lymphoblastoid human B cell line 721.221. In the knock down experiments, prior to the mixing with 721.221 and 721.221-Cw3 cells, KIR-CD300a WT Jurkat T cells were transfected with 400 μM of the indicated siRNA duplexes using the Amaxa Nucleofection System (Lonza). After 36 hours, the efficiency of the knock down was measured at the mRNA and protein levels by real-time PCR and western blot analysis, respectively. The percentage of inhibition of CD69 expression was calculated according to the following formula: [(SED loaded 721.221 Mediated CD69 induction – SED loaded 721.221-Cw3 Mediated CD69 Induction)/SED loaded 721.221 Mediated CD69 induction] x 100. CD69 expression was measured by median fluorescence intensity (MFI).
NFAT luciferase reporter assays
DT40 chicken B cells expressing CD300a or Jurkat T cells expressing the chimeric KIR-CD300a receptor were transiently transfected with 5 μg of an NFAT luciferase reporter construct and cultured for 16 hours. For experiments with B cells, DT40 transfectants were distributed into duplicate wells of a 24 well plate containing medium alone, prebound anti-mouse IgG plus anti-chicken IgM and either isotype IgG1 control antibody or anti-CD300a mAb. For experiments with T cells, Jurkat transfectants were mixed with an equal number of 721.221 cells and added to wells of a 24 well plate with or without the superantigen, SED (100 ng/ml). As a measure for maximal NFAT activity, cells were treated with 50 ng/ml phorbol myristate acetate (PMA) plus 5 μM ionomycin, purchased from EMD. After 6 h, cells were disrupted in lysis buffer (Promega) and lysates were assayed using luciferin (Promega).
Calcium mobilization assays
DT40 chicken B cells, 1.5 x 106, were washed with PBS containing 1% BSA, resuspended in 3 ml and loaded with 3 μg of Fluo-4 and 7.5 μg of Fura-Red (Invitrogen) for 30 minutes at 30°C. Then, cells were washed twice and aliquots of 1 ml were warmed at 37°C for 5 minutes, followed by acquisition in a flow cytometer (FACS Calibur). To establish a baseline, cells were first acquired for 30 seconds, at which point the anti-IgM mAb plus the anti-CD300a mAb or isotype control IgG1 were added and acquisition was followed for another 30 seconds. Then, the secondary antibody was added and acquisition was followed for 5–6 minutes. Data were analyzed using the FlowJo software (Treestar).
Data were analyzed using GraphPad Prism software. The data were plotted as bar graphs or scatter plots, and pair wise comparisons were examined by two-tailed paired Student’s t-test. NS: non significant; * P < 0.05, ** P < 0.01; *** P < 0.001.
We thank Dr. Lynde Meyaard for the phosphatase deficient DT40 chicken B cells, Dr. John E. Coligan for the 721.221 cells and Dr. Eric O. Long for plasmids encoding the phosphatases and KIR2DL2. This work was funded by the intramural program of the Food and Drug Administration.
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