SLP-65: A New Signaling Component in B Lymphocytes which Requires Expression of the Antigen Receptor for Phosphorylation

Immobilized PT66 antiphosphotyrosine-agarose beads (Sigma-Aldrich, Deisenhofen, Germany) and soluble 4G10 antiphosphotyrosine antibodies (Upstate Biotechnology Inc., Lake Placid, NY) were used for precipitation and immunoblot analysis of phosphotyrosine-containing proteins, respectively. Anti-Vav and anti–Grb-2 rabbit polyclonal antibodies were purchased from Santa Cruz Biotechnology Inc. (Santa Cruz, CA). Polyclonal anti–SLP-65 antibodies were produced by immunizing rabbits with KLH-coupled SLP-65 peptides encompassing amino acids 148–161 (KARLA peptide; see Fig. 1). The glutathione S-transferase (GST)–Grb-2 fusion proteins contain amino acids 1–168 (SH3-SH2) and 49–168 (SH2) of the human Grb-2 protein, respectively. Primer sequences used for amplifications of the respective Grb-2 cDNA fragments are available upon request. The plasmid encoding the GST–Grb-2 (SH3) fusion protein was a gift of Dr. William Wishart, Novartis (Basel, Switzerland). The GST fusion protein encompassing the complete murine Grb-2 was obtained from Upstate Biotechnology Inc.

J558L cell lines, pervanadate/H₂O₂ stimulations, immunoprecipitations, affinity purifications with GST fusion proteins, and Western blot analysis were described previously (5, 8).

In total, 10¹⁰ J558Lδm7.1 cells were stimulated in aliquots of 3 × 10⁷ cells per ml RPMI 1640 medium for 3 min with 50 μM pervanadate/H₂O₂ at 37°C (5). After lysis of the cells in 600 μl of 1% NP-40 lysis buffer (5), postnuclear supernatants were collected and precleared for 3 h with 7.5 ml of mouse IgG agarose (Sigma-Aldrich). Subsequently, the lysate was subjected to antiphosphotyrosine immunoprecipitation with 6 ml of agarose-conjugated PT66 mAb (Sigma-Aldrich). Settled beads were extensively washed with 1% NP-40 lysis buffer, and bound proteins were eluted eight times with 7.5 ml 50 mM phenyl phosphate/200 mM NaCl. Proteins were concentrated with centrifugal filter devices (microsep 10K; Pall Filtron Corp., East Hills, NY), separated by 10% SDS-PAGE, and stained with Coomassie blue. The 65-kD protein band was excised, subjected to in-gel digestion with lysyl endopeptidase C (Lys-C), and the resulting HPLC-purified peptides were sequenced (TOPLAB, Munich, Germany; see Fig. 1).

Several independent clones of a 2-kb cDNA (GenBank accession no. Y17159) were isolated using a combination of standard PCR with primers derived from a partial cDNA sequence in GenBank (accession no. AJ222814) and 5′ rapid amplification of cDNA ends (5′RACE; GIBCO BRL, Gaithersburg, MD) and completely sequenced.

As described previously (9), total cellular RNA was isolated, and 15 μg per sample was separated in a denaturing agarose gel. After blotting, hybridization was performed with a randomly primed 795-bp PstI fragment from nucleotide 650 to 1445 (the open reading frame [ORF] extends from 478 to 1851).

For transient expression of SLP-65 in J558Lμm3 cells, a 1490-bp PCR fragment (amplified with PfuI [Stratagene Inc., La Jolla, CA]) containing the entire ORF was cloned downstream of the CMV promoter in pCGN (10). The resulting expression vector, pCGN-p65, encodes a SLP-65 fusion protein containing an NH₂-terminal, 20 amino acid peptide tag which is derived from the hemagglutinin protein of human influenza virus (HA tag [11]). The conditions for electroporation have been described previously (9).

To identify PTK substrate proteins in B cells, we affinity purified these proteins from the lysate of pervanadate/ H₂O₂-stimulated J558Lδm7.1 cells via antiphosphotyrosine antibody columns and determined their peptide sequence. We focused on a 65-kD protein which is the most rapidly phosphorylated substrate after exposure of J558Lδm7.1 cells to antigen or to pervanadate. Several of the sequenced peptides matched with a partial sequence in GenBank (accession no. AJ222814). Using mouse splenic cDNA as template, we used a combination of conventional and 5′RACE PCR to isolate ∼2 kb of the corresponding cDNA (accession no. Y17159). The cDNA we obtained has an ORF encoding a protein of 457 amino acids (Fig. 1,A). Seven of the peptides sequenced from the purified protein were found in the predicted sequence (Fig. 1,A, underline). The NH₂-terminal portion of the protein contains seven tyrosine residues which are putative targets for phosphorylation (Fig. 1,A, dots). Five of these are found in a YxxP context otherwise found in the PTK substrates Cas, p62dok, Cbl, and SLP-76 (12–15). The central part of the protein is rich in prolines and contains several SH3 domain–binding motifs. The COOH-terminal part contains an SH2 domain which, when compared with the database, is most similar to the SH2 domain of SLP-76, a recently identified PTK substrate in T lymphocytes (15). Both proteins share the same overall structure. A comparison with human and mouse SLP-76 also reveals a modest similarity in the NH₂ terminus (not shown). We conclude that the 65-kD protein substrate is the B cell analogue of SLP-76, and call it SLP-65. In a Northern blot analysis, the 2-kb SLP-65 transcript is found only in spleen and weakly in thymus, but not in liver, testis, or brain (Fig. 1,B). The transcript is also found in B cell lines representing different developmental stages from the pre-B to the plasma cell stage, but not in a T cell or a fibroblast line (Fig. 1 B). These results suggest that SLP-65 is primarily expressed in B lymphocytes but perhaps to some extent also in thymocytes.

SLP-65 has a predicted pI of 8.2, in good agreement with our experimental data showing a pI of 8.5 (data not shown). The predicted molecular mass of 50.7 kD is considerably smaller than the apparent size of 65 kD in SDS-PAGE. To test whether this could be due to aberrant migration, and to obtain further evidence that we had indeed isolated the cDNA encoding the tyrosine-phosphorylated 65-kD substrate, we transiently expressed SLP-65 in J558Lμm3 cells as a fusion protein with an NH₂-terminal HA tag (see Materials and Methods). Anti–SLP-65 peptide antibodies (see Materials and Methods) precipitated the HA-tagged fusion protein from pervanadate/H₂O₂-stimulated J558Lμm3 transfectants but not from control cells. The HA-tagged SLP-65 migrates slightly above the endogenous SLP-65 as detected by antiphosphotyrosine antibodies (Fig. 1 C) and anti-HA antibodies (data not shown). We conclude that the cDNA we isolated encodes the 65-kD substrate for activated PTKs.

In T cells, the SLP-76 adaptor protein is bound by Grb-2 and Vav (16–18). Anti–SLP-65 antibodies, but not the preimmune serum, coprecipitate Grb-2 and Vav from lysates of unstimulated and pervanadate/H₂O₂-stimulated J588Lμm3 cells (Fig. 2, lanes 2 and 4). The phosphorylated form of SLP-65 is only found in the lysates of pervanadate/ H₂O₂-stimulated cells (Fig. 2, top, lane 4). These data show that SLP-65 is constitutively associated with Grb-2 and Vav, supporting the notion that SLP-65 is the B cell analogue of SLP-76. Using different GST–Grb-2 fusion proteins, SLP-65 could be purified from lysates of unstimulated and pervanadate/H₂O₂-stimulated J558Lμm3 cells with the NH₂-terminal SH3 domain of Grb-2 (Fig. 3, bottom, lanes 1 and 2) and to an even stronger extent with the combined SH3 and SH2 domains (Fig. 3, lanes 3 and 4). SLP-65 bound only weakly to the SH2 domain of Grb-2 and not at all to GST alone (Fig. 3, lanes 5, 6, 9, and 10). Probing the same blot with antiphosphotyrosine antibodies showed that, in addition to SLP-65, the Grb-2 SH3 domain coprecipitates a phosphoprotein of 110 kD. This protein may be identical or similar to the SLP-76–associated protein SLAP130/FYB (19, 20). These proteins, as well as other phosphoproteins, were more efficiently purified by the combination of the SH3 and SH2 domains of Grb-2 but not by GST alone (lanes 4 and 10). Two proteins with characteristics similar to SLP-65 have been also found in a human B cell line (21).

We have previously shown that after exposure to pervanadate, a 65-kD protein is rapidly phosphorylated only in BCR-positive cells (5). To verify that SLP-65 is identical to this early PTK substrate, we stimulated the BCR-negative J558L line and its BCR-positive transfectant J558Lμm3 for different times with pervanadate/H₂O₂. Similar amounts of SLP-65 were purified from these cells with the GST–Grb-2[SH3-SH2] fusion protein (Fig. 4, bottom, lanes 1–6). However, the SLP-65 protein remained completely unphosphorylated in the BCR-negative line, even after 2 min of stimulation (Fig. 4, top, lane 3). In the BCR-positive transfectant, SLP-65 is rapidly phosphorylated, 10 s after stimulation (lane 5). Other PTK substrate proteins in the BCR-negative and -positive lines require longer times of stimulation for detection with antiphosphotyrosine antibodies (Fig. 4, top, lanes 3 and 6). Thus, the rapid phosphorylation of SLP-65 in J558Lμm3 B cells is dependent on the BCR surface expression.

Our data suggest that SLP-65 is part of a BCR transducer complex comprising not only kinases, phosphatases, and their substrates, but also adaptor proteins which are necessary to physically and functionally connect these elements. This may be a common theme in signal transduction (6, 7). The early and BCR-dependent phosphorylation of SLP-65, together with its restricted expression pattern, suggest that SLP-65 is critically involved in coupling intracellular signaling elements specifically to the BCR. This may contribute to a basal level of signaling in the absence of antigen, a mechanism that may be necessary for B cell maintenance (22, 23). Such a central role in signal transduction is also suggested for SLP-76. Overexpression of SLP-76 in T cells can augment signal transduction from the TCR, leading to increased nuclear factor of activated T cells (NFAT) activation and IL-2 secretion (24, 25). Furthermore, mice deficient for SLP-76 contained no peripheral T cells as a result of an early block in T cell development, whereas B cells develop normally (26). To better understand the function of the SLP protein family, it will be necessary to reveal exactly how they are connected to the antigen receptors.

We thank Dr. Lise Leclercq for critical reading of the manuscript.

This work is supported by the Deutsche Forschungsgemeinschaft through SFB 388, and by the Leibniz program.

BCR

B cell antigen receptor

GST

glutathione S-transferase

HA

hemagglutinin

ORF

open reading frame

PTK

protein tyrosine kinase

RACE

rapid amplification of cDNA ends

SH2 and SH3 domain

Src homology 2 and 3 domain, respectively

SLP-65

SH2 domain–containing leukocyte protein of 65 kD