|Home | About | Journals | Submit | Contact Us | Français|
The sensitivity of primary splenic B cells to Fas-mediated apoptosis is modulated in a receptor-specific fashion. Here we used a differential display strategy to detect cDNAs present in B cells rendered Fas resistant but absent in those rendered Fas sensitive. This led to the cloning and characterization of a novel 1.2-kb gene that encodes a Fas apoptosis inhibitory molecule (FAIM). faim-transfected BAL-17 B lymphoma cells were less sensitive by half or more to Fas-mediated apoptosis than were vector-transfected controls, using Fas ligand–bearing T cells or a cytotoxic anti-Fas antibody to trigger Fas, and this was associated with inhibition of Fas- induced poly-ADP ribose polymerase (PARP) cleavage. In primary B cells, the time course of faim mRNA and FAIM protein expression correlated with the induction of Fas resistance by surface (s)Ig engagement. Thus, FAIM is an inducible effector molecule that mediates Fas resistance produced by sIg engagement in B cells. However, faim is broadly expressed in various tissues and the faim sequence is highly conserved evolutionarily, suggesting that its role extends beyond lymphocyte homeostasis. As FAIM has no significant regions of homology to other gene products that modulate Fas killing, it appears to represent a distinct, new class of antiapoptotic protein.
The Fas/Fas ligand (FasL)1 system is one of an expanding family of receptor–ligand pairs involved in cell fate determination in a variety of cell types, notably including those of lymphoid origin (1). Fas engagement initiates an intracellular signaling cascade through oligomerization of caspase 8, mediated via the adaptor protein FADD, which contains both death and death effector homologous domains (2). Caspase 8 appears to be the most proximal of several ICE-like proteases whose sequential activation is responsible for the apoptotic demise of the cell (3–6). Fas engagement also triggers mitochondrial cytochrome c release that, in conjunction with apoptotic protease-activating factor (APAF)-1 and dATP, activates caspase 9 and downstream caspases (7–11). Fas signaling for cell death may be modulated by several distinct antiapoptotic proteins, which directly bind Fas, inhibit caspase activity or activation, or modulate mitochondrial events (9, 10, 12–21).
We and others have shown that the susceptibility of primary B cells to Fas-mediated apoptosis is regulated in a receptor-specific fashion (22–24). Engagement of CD40 upregulates Fas expression and renders B cells sensitive to Fas-mediated apoptosis, whereas concurrent or sequential signaling through the B cell antigen receptor induces a state of Fas resistance (22). Induction of Fas resistance develops progressively over a period of hours, and depends on macromolecular synthesis, suggesting that protection against Fas killing requires the induction and accumulation of one or more gene products (reference 25 and our unpublished observations). Indeed, we recently demonstrated that Bcl-xL expression is upregulated in primary B cells that have been rendered Fas resistant, and showed that overexpression of Bcl-xL diminishes Fas-mediated apoptosis in CD40L-stimulated B cells obtained from transgenic mice (26). However, a role for other gene products is suggested by three observations. First, Bcl-xL–overexpressing B cells were not completely protected from Fas killing (26). Second, treatment of Bcl-xL–overexpressing B cells with anti-Ig produced additional inhibition of Fas-mediated apoptosis (26). Third, Bcl-xL protein appeared in normal B cells after, not before, the first manifestations of anti-Ig–induced Fas resistance (25, 26). These results raise the possibility that additional gene products, induced by surface (s)Ig cross-linking, contribute to Fas resistance. Herein we describe the use of differential display to elucidate, in an unbiased fashion, inducible factors that modulate susceptibility to Fas-mediated apoptosis in B cells, and report the identification of a gene that, when overexpressed in a model B cell line, reduces Fas sensitivity and thus codes for a Fas apoptosis inhibitory molecule termed FAIM.
Male Balb/cByJ mice at 8–14 wk of age were obtained from The Jackson Laboratory. Mice were housed at least 1 wk before experimentation. Mice were cared for and handled at all times in accordance with the National Institutes of Health and our institutional guidelines.
Splenic B cells from 8–12-wk-old naive Balb/cByJ mice were purified and depleted of T cells and macrophages as previously described (22). RBCs and nonviable cells were removed by sedimentation over Lympholyte M (Cedarlane Labs., Canada). The resulting B cells were cultured at 37°C with 5% CO2 in RPMI 1640 medium (BioWhittaker) supplemented with 5% heat-inactivated fetal bovine serum (Sigma Chemical Co.), 10 mM Hepes (pH 7.2), 50 μM 2-ME, 2 mM l-glutamine, 100 U/ml penicillin, and 100 μg/ml streptomycin.
Total RNA was prepared from primary murine splenic B cells stimulated with CD40L/CD8α fusion protein cross-linked with anti-CD8 antibody (CD40L) for 48 h, in the absence or presence of F(ab′)2 fragments of polyclonal goat anti–mouse IgM (anti-Ig) added for the final 6 h of the culture period, using Phenol/GITC (Sigma Chemical Co.; 27). Reverse transcription and differential display were performed as previously described (28) using the RNAImage Kit (GenHunter). Putatively differentially expressed cDNA fragments were excised from dried sequencing gels, eluted in dH2O, and reamplified using the same primer pair originally used in differential display. These fragments were tested for differential expression by Northern blot analysis; PCR products confirmed by this assay were subcloned into a TA cloning vector (Invitrogen). Plasmid DNA from individual clones was radiolabeled and used to probe additional Northern blots in order to identify the insert responsible for differential expression. Subcloned Northern blot–positive cDNAs were subject to automated fluorescent DNA sequencing (Applied Biosystems) and analyzed by comparison to standard sequencing databases in the public domain (BLAST; National Center for Biotechnology Information).
Total RNA was prepared from primary murine splenic B cells using UltraSpec RNA isolation reagent (Biotecx Laboratories). Purified RNA was electrophoresed on a 1% agarose/formaldehyde gel, transferred to GeneScreen Plus (NEN) in 10× SSC and hybridized to a 234-bp radiolabeled fragment of faim generated by PCR, using the primers CTGGATGGCGAGGACCTGAG (5′) and GGTGTCACTGAGTGAGCTCTG (3′). Initial Northern probing to confirm differential expression was performed as above except that differential display primers were used and the annealing step of PCR was performed for 2 min at 40°C. Autoradiography was performed using intensifying screens at −80°C for 1–3 d. A multiple tissue Northern blot was obtained from OriGene Technologies.
A radiolabeled probe generated as described above was used to screen a directional murine thymic cDNA library that was constructed in pBKCMV (Stratagene) and was provided by Dr. Adam Lerner (Boston University Medical Center, Boston, MA). Plaque lifts were performed using Protran membranes (Schleicher and Schuell). A number of individual clones from among 106 plaques were sequenced, leading to the isolation of a full-length clone as determined by an in-frame stop codon upstream of the start methionine. This clone encodes a novel 179–amino acid protein as discussed below.
Mid-log phase BAL-17 B lymphoma cells in suspension were transfected with 20 μg faim-containing plasmid or pBKCMV empty vector (plus 500 μg carrier salmon sperm DNA) by electroporation at 276 V and 550 μF using a Gene Pulser apparatus (Bio-Rad). Transfected cells were immediately plated to prewarmed medium and cultured at 37°C with 5% CO2 as above (29). After 2 d, transfected cells were split 1:15 into fresh medium containing 2 mg/ml G418 (Sigma Chemical Co.) to obtain pools of transfectants. Separately, individual stably transfected clones were isolated by limiting dilution in medium containing G418.
BAL-17 transfectants stimulated for 24 h with CD40L were tested as targets in standard 4-h, lectin-dependent 51Cr-release assays with AE7 CD4+ Th1 effector cells at effector/target cell ratios of 0.3:1 to 9:1, as previously described (22, 25), or with Jo-2 anti-Fas antibody (PharMingen) at 50, 5, or 0.5 ng/ml. Alternatively, nuclei obtained from CD40L-stimulated BAL-17 transfectants were stained with propidium iodide and the level of subdiploid DNA was determined by flow cytometry, as described (30).
B cell protein lysates were resolved by 15% SDS-PAGE, transferred to Hybond nitrocellulose membranes (Amersham), and blocked with 5% nonfat dry milk in TBS-Tween 20 (TBS-T) for 1 h at room temperature. Membranes were probed with anti-PARP antibody 2-C-10 (Calbiochem) at 1:500 in TBS-T. After washing, blots were incubated with horseradish peroxidase–conjugated goat anti–mouse IgG and developed by enhanced chemiluminescence (NEN), as previously described (31).
B cells were stained with PE-conjugated Jo-2 Fas-specific antibody or anti-TNP isotype control antibody (PharMingen) in the presence of 2% normal rabbit serum and 2.4G2 (anti-FcR) antibody, as previously described (32). Relative fluorescence intensity was detected by flow cytometry with a FACScan® instrument (Becton Dickinson).
Two peptides (amino acids 57–68 and 125–138) corresponding to predicted hydrophilic regions of the FAIM open reading frame (33) were synthesized by Research Genetics Corp. These peptides contain an NH2-terminal cysteine followed by an amino-caproic acid. Each peptide (2 mg) was separately coupled to KLH (Pierce Chemical Co.); the coupled peptides were combined and used to generate anti-FAIM peptide antibodies in chickens (Aves Labs.). B cell protein lysates were resolved by 15% SDS-PAGE, transferred to Hybond nitrocellulose membranes (Amersham), and blocked with 10% Blok-Hen blocking reagent (Aves Labs.) for 1 h at room temperature. The nitrocellulose filters were then probed with FAIM-specific antibodies diluted 1:1,000 in TBS-T containing 10% Blok-Hen for 1.5 h at room temperature. After washing, blots were incubated with horseradish peroxidase–conjugated goat anti–chicken IgY (Aves Labs.) for 1 h and developed by enhanced chemiluminescence (NEN) as described (31).
Affinity purified F(ab′)2 fragments of polyclonal goat anti–mouse IgM were obtained from Jackson ImmunoResearch Labs. and used at 10 μg/ml. Soluble rCD40L was obtained from transfected J558L cells that secrete a chimeric CD40L/ CD8α fusion protein (34), which was collected and dialyzed against 25,000 mol wt cut-off dialysis tubing, as previously described (35). A similarly dialyzed supernatant containing anti-CD8 antibody from the 53-6-72 hybridoma was used to cross-link the fusion protein. CD40L and anti-CD8 containing supernatants were used at final dilutions of 1:10 and 1:80, respectively. G418 was obtained from GIBCO BRL. An expressed sequence tag (EST) encompassing putative human FAIM was obtained from the I.M.A.G.E. consortium (36). 51Cr was obtained from NEN.
In previous work we showed that B cell treatment with anti-Ig for only the final 1–12 h of a 48-h culture with CD40L produced a time-dependent increase in Fas resistance that was abrogated by cycloheximide (25). Additional experiments demonstrated that the induction of Fas resistance in CD40L-stimulated B cells by anti-Ig treatment for 6 h was completely blocked by the addition of actinomycin D (data not shown). These results strongly suggest that transcriptional activation and gene expression are required for the receptor-specific induction of the Fas-resistant state. For this reason, genes that oppose Fas-mediated apoptosis might be captured by identifying transcripts expressed uniquely in Fas-resistant B cells.
To identify genes expressed coordinately with the induction of Fas resistance, we used a differential display strategy (28). RNA was extracted from B cells stimulated with CD40L alone for 48 h (Fas-sensitive) and from B cells stimulated with CD40L (for 48 h) plus anti-IgM for the final 6 h of culture (Fas-resistant), and was reverse transcribed. Application of arbitrary decameric primer pairs to these cDNA populations permitted reproducible amplification of a number of transcripts present in Fas-resistant B cells but absent in their Fas-sensitive counterparts. These amplified gene fragments were excised and used as probes in Northern blots of RNA obtained from Fas-sensitive and Fas-resistant primary B cells to confirm differential expression (Fig. (Fig.11 A). Of 40 such fragments, 8 failed to reamplify. Of the remaining 32, 8 displayed differential expression by Northern blot analysis. One of these recognized an ~1.2-kb transcript on Northern blot (Fig. (Fig.11 A) that was widely expressed in multiple tissues, with the highest levels present in murine brain, thymus, kidney, and spleen (Fig. (Fig.11 B). This transcript was chosen for further analysis.
Using a radiolabeled probe generated by PCR, a murine thymic cDNA library was screened and the DNA from positive plaques was sequenced. A number of overlapping clones were identified whose consensus sequence was ~1.2 kb, consistent with the expression data described above. Subsequently a full-length clone was identified that contained an in-frame STOP codon upstream of the START methionine, and possessed, in the 3′ UTR, an RNA instability motif, polyA+ consensus motifs and a polyA+ tail (37). This cDNA appeared to encode a novel 179–amino acid open reading frame (Fig. (Fig.2).2). Structural analysis predicted a β-strand–rich, stable, soluble protein with a slightly acidic pI (pH 5.4). No substantial regions of homology with any other sequence are present.
To determine the capacity of the isolated cDNA clone to produce resistance to Fas-mediated apoptosis, BAL-17 murine B lymphoma cells were transfected with the pBKCMV expression vector. BAL-17 cells were chosen because their activation responses mimic primary B cells in a variety of ways and they are readily transfectable (38–40). Like primary B cells, unstimulated BAL-17 B cells express little Fas, but treatment with CD40L induces Fas expression and sensitivity to Fas-mediated apoptosis (data not shown). After electroporation, pools of BAL-17 B cells stably transfected with either full-length cDNA or empty vector were selected in G418 for 2 wk. These two populations differed in their susceptibility to Fas killing induced by FasL-bearing Th1 effector cells: at each effector/target cell ratio tested, specific lysis of cDNA-transfected BAL-17 B cells, detected by Cr-release assay, was reduced by half or more in comparison to cells transfected with vector alone (Fig. (Fig.33 A), despite equivalent levels of surface Fas expression (data not shown). These results suggest a level of protection of ninefold or more, in terms of the effector/target ratio required to produce equivalent levels of apoptosis in faim- and vector-transfected BAL-17 B cells. The reduction in Fas killing was also apparent when cytotoxicity was induced by lytic Jo-2 anti-Fas antibody (data not shown). In addition, stably transfected clones were isolated by limiting dilution and tested for susceptibility to Fas killing. The results obtained with individual clones completely mimicked those obtained with G418-resistant pools in that Fas-mediated apoptosis (produced by Jo-2) was reduced by one-half to two-thirds in stably transfected cDNA-expressing BAL-17 B cells in comparison to BAL-17 cells transfected with empty vector, as detected by propidium iodide staining for subdiploid DNA (Fig. (Fig.33 B). These data indicate that the novel cDNA transcript initially identified in inducibly Fas-resistant B cells codes for a Fas apoptosis inhibitory molecule (FAIM) that counteracts Fas signaling for cell death when overexpressed.
To characterize the nature of the FAIM-induced block in Fas signaling for cell death, the fate of PARP, a terminal caspase cleavage product, was examined by Western blot of size-separated whole cell extracts (41). Proteolytic fragments of PARP were readily detected when vector-transfected BAL-17 B cells were treated for 40 min with Jo-2 anti-Fas antibody. In contrast, there was little or no PARP cleavage in faim-transfected BAL-17 B cells up to 60 min after anti-Fas treatment (Fig. (Fig.33 C). Thus, FAIM blocks Fas apoptosis at a step proximal to the cleavage of the caspase substrate, PARP.
As a control for these experiments, FAIM expression in faim- and vector-transfected BAL-17 B cells was determined by Western blotting with polyclonal anti-FAIM antibody. Antibody was prepared by immunizing chickens with two relatively hydrophilic peptides derived from the FAIM sequence (amino acids 57–68, DGKEEIRREWMF; and 125–138, RLDGEDLRVVLEKD) coupled to KLH; the resultant antibody (purified from the IgY fraction of egg yolks) specifically recognized a protein of the expected size, ~20 kD, on Western blot, whereas pre-immune IgY did not. Using this antibody, the expression of FAIM protein was found to be much increased in faim-transfected, as opposed to vector-transfected, BAL-17 B cells (Fig. (Fig.33 C).
To further evaluate the association between FAIM expression and inducible Fas resistance, primary B cells were studied by Northern and Western blotting after stimulation with CD40L and anti-Ig. CD40L stimulation alone, which induces Fas expression and Fas sensitivity, elicited little or no increase in faim expression over the low basal level present in unstimulated B cells. However, addition of anti-IgM, which induces Fas resistance, to CD40L-stimulated B cells produced a marked, time-dependent increase in faim mRNA, beginning at 1 h and reaching a maximum after 6 h of anti-Ig treatment (Fig. (Fig.44 A). Similar results were obtained when the expression of FAIM protein was monitored. FAIM was absent in unstimulated B cells and B cells stimulated for 48 h with CD40L alone; however, addition of anti-IgM to CD40L-stimulated B cells produced a marked increase in FAIM protein, first seen after 18 h of anti-Ig treatment (Fig. (Fig.44 B). In some experiments FAIM protein expression was detected after 6 h of anti-Ig treatment (data not shown).
The correlation between sIg-induced FAIM expression and Fas resistance was tested further by examining tolerant, autoreactive B cells obtained from double transgenic, anti– hen egg lysozyme (HEL)/HEL mice. In these B cells, in vitro studies showed that specific antigen (soluble [s]HEL) is an insufficient stimulus to produce Fas resistance, whereas Fas resistance is induced by more extensive sIg cross-linking with anti-Ig (42). In keeping with this, sHEL failed to induce upregulation of FAIM protein expression in B cells drawn from double transgenic anti-HEL/HEL mice, whereas FAIM protein was induced by anti-Ig in these B cells (Fig. (Fig.44 C). In this situation, as with anti-Ig–treated B cells from normal mice, above, induction of FAIM expression correlates with production of Fas resistance.
To evaluate the possibility that faim is phylogenetically conserved, public databases were searched for evidence of similar genes in other species. Human faim was obtained by identifying a consensus sequence from overlapping human ESTs with homology to mouse faim, followed by sequencing of a single EST clone that completely spanned putative human faim (36). The consensus/EST sequence was used to predict an amino acid sequence, which showed human FAIM to be 90% identical to the predicted amino acid sequence of mouse FAIM (see Fig. Fig.2).2). These results are complemented by Southern blot analysis of genomic DNA showing hybridization by a mouse faim probe to all mammalian species tested (human, monkey, rat, mouse, dog, cow, and rabbit; data not shown).
C. elegans FAIM was obtained by amplifying cDNA with primers based on the predicted exon structure of a random genomic sequence of unknown function, and then sequencing the resultant DNA. The predicted amino acid sequence of this C. elegans FAIM is 50% identical to the predicted amino acid sequence of mouse FAIM (see Fig. Fig.2).2). The extensive evolutionary conservation manifest in the sequences of human, mouse, and C. elegans faim strongly suggests that the faim gene product is a key apoptotic regulatory molecule that has been retained with minimal change throughout phylogeny.
Fas engagement contributes to cell fate determination in a variety of cell types, and plays an important role in modulating immune responses and regulating autoreactive B lymphocytes (23, 42). The results reported here identify a novel gene, isolated by differential display (28) and termed faim, that opposes Fas-mediated apoptosis when overexpressed in a model B cell line, and whose expression in primary B cells is coordinately regulated with sIg signals that block Fas killing. Thus, FAIM is an inducible effector molecule that mediates Fas resistance produced in B cells by sIg engagement, and does so by blocking a step in the Fas signaling pathway before the activation of caspase 3, an effector caspase responsible for PARP cleavage (41). The influence of FAIM appears to be specific to Fas-induced cell death, because BAL-17 B cells stably transfected with faim are not more resistant to apoptosis produced by staurosporine or ultraviolet radiation than vector-transfected controls (data not shown). As FAIM bears no regions of homology with other gene products that modulate Fas killing, it appears to represent a distinct new class of antiapoptotic protein.
Overexpression of FAIM in stably transfected BAL-17 B cells produced substantial, but less than complete, resistance against Fas-mediated apoptosis, and was less effective in blocking Fas killing than optimal sIg signaling in primary B cells. This suggests that receptor-mediated Fas resistance in primary B cells cannot be explained on the basis of FAIM induction alone. Recently we reported that Bcl-xL is induced in primary B cells after sIg engagement that produces Fas resistance, and that the Fas sensitivity of CD40L-stimulated B cells from Bcl-xL overexpressing transgenic mice was substantially reduced compared with littermate control B cells (26). These results infer a key role for Bcl-xL in sIg-mediated Fas resistance. However, further inhibition of susceptibility to Fas-mediated apoptosis in Bcl-xL transgenic B cells was produced by anti-Ig treatment, implicating additional antiapoptotic factors (26). Thus, sIg-triggered Fas resistance may result, at least in part, from the combined effects of inducible FAIM and Bcl-xL expression. In support of this, Fas-resistant faim transfectants express no more Bcl-xL than do vector-transfected controls (data not shown), so there is no direct linkage between FAIM and Bcl-xL, the only other antiapoptotic gene presently implicated in B cell Fas resistance. Thus, inducible resistance against Fas is multigenic in nature. Although FAIM and Bcl-xL may inhibit separate and distinct intracellular pathways leading from Fas to terminal apoptotic events (43), the possibility that these antiapoptotic molecules interfere with the same death mediators has not been ruled out. Notably, the multigenicity of inducible protection against Fas killing suggests the intricacy of regulatory controls asserted over apoptotic death by environmental cues.
FAIM shares no regions of homology with known antiapoptotic proteins and contains no known protein–protein interaction motifs, implying that an as yet unidentified structure is responsible for its antiapoptotic function. Preliminary results suggest that the activity of this structure is broad and crosses species boundaries, in that human HeLa cells transiently transfected with mouse faim display Fas resistance in comparison to vector-transfected controls (data not shown). Moreover, FAIM-like genes are expressed in other species, including C. elegans. In fact, the degree of amino acid identity between C. elegans and mouse FAIM (50%) is much greater than that between C. elegans ced-3 and mouse ICE, and between C. elegans ced-9 and mouse bcl-2 (both <25%), two pairs of genes with accepted similar functions related to apoptosis (44, 45). This remarkably high degree of evolutionary conservation across a broad phylogenetic chasm suggests that FAIM plays a key role in cellular physiology. Furthermore, three specific regions of FAIM, encompassing 21, 17, and 17 amino acids, respectively, exceed 75% identity between mouse, human, and C. elegans FAIM; one or more of these regions may well be indispensable to the antiapoptotic function of FAIM.
This work was supported by United States Public Health Service grant AI40181 awarded by the National Institutes of Health, and by a grant from the Arthritis Foundation.