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Dengue virus M protein contains a proapoptotic sequence referred to as ApoptoM

Olga Kalinina^1,

Marie-Pierre Courageot^1,

¹ Unité Postulante des Interactions Moléculaires Flavivirus-Hôtes, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France
² Plate-Forme de Cytométrie, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France
³ Unité de Biologie des Infections Virales Emergentes, Institut Pasteur, Lyon, France

Correspondence
Philippe Desprès
pdespres{at}pasteur.fr

	ABSTRACT

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The induction of apoptotic cell death is a prominent cytopathic effect of dengue (DEN) viruses. One of the key questions to be addressed is which viral components induce apoptosis in DEN virus-infected cells. This study investigated whether the small membrane (M) protein was involved in the induction of apoptosis by DEN virus. This was addressed by using a series of enhanced green fluorescent protein-fused DEN proteins. Evidence is provided that intracellular production of the M ectodomains (residues M-1 to M-40) of all four DEN serotypes triggered apoptosis in host cells such as mouse neuroblastoma Neuro 2a and human hepatoma HepG2 cells. The M ectodomains of the wild-type strains of Japanese encephalitis, West Nile and yellow fever viruses also had proapoptotic properties. The export of the M ectodomain from the Golgi apparatus to the plasma membrane appeared to be essential for the initiation of apoptosis. The study found that anti-apoptosis protein Bcl-2 protected HepG2 cells against the death-promoting activity of the DEN M ectodomain. This suggests that the M ectodomain exerts its cytotoxic effects by activating a mitochondrial apoptotic pathway. The cytotoxicity of the DEN M ectodomain reflected the intrinsic proapoptotic properties of the nine carboxy-terminal amino acids (residues M-32 to M-40) designated ApoptoM. Residue M-36 was unique in that it modulated the death-promoting activity of the M ectodomain. Defining the ApoptoM-activated signalling pathways leading to apoptosis will provide the basis for studying how the M protein might play a key role in the fate of the flavivirus-infected cells.

Present address: Pasteur Institute of Saint Petersburg, U1 Mira 14, 197101 Saint Petersburg, Russia.

Present address: Laboratoire des Biomembranes et Messagers Cellulaires, CNRS-UMR 8619, Université Paris XI, Orsay, France.

	INTRODUCTION

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Mosquito-borne flaviviruses such as dengue (DEN), Japanese encephalitis (JE), Saint Louis encephalitis (SLE), West Nile (WN) and yellow fever (YF) viruses may cause epidemic disease outbreaks in humans. Infected patients may exhibit a wide range of acute diseases, from nonspecific febrile illness to severe haemorrhagic manifestations (DEN and YF) or encephalitic syndromes (JE, SLE and WN). Flaviviruses (family Flaviviridae) are single-stranded, enveloped RNA viruses (Chambers et al., 1990; Rice, 1996). The virion consists of three structural proteins: C (core protein), M (membrane protein) and E (envelope protein) (Chambers et al., 1990; Rice, 1996). The virion is first assembled as an immature particle, in which prM (the intracellular precursor of M) is noncovalently associated with E in a heterodimeric complex. Late in virus morphogenesis, prM is processed by subtilisin-like proteases to generate the mature M protein (Chambers et al., 1990; Rice, 1996). The M protein (7–9 kDa) consists of a 40 amino acid long ectodomain followed by the transmembrane-anchoring region including two transmembrane domains (TMDs) (Chambers et al., 1990; Rice, 1996). Three-dimensional imaging of the structure of the DEN virion, showing the location of the M protein with respect to the E homodimer, was recently carried out (Kuhn et al., 2002). Several studies have shown that the M ectodomain induces a neutralizing antibody response (Bray & Lai, 1991; Vazquez et al., 2002).

All four serotypes of DEN virus (DEN-1, DEN-2, DEN-3 and DEN-4) and JE, Langat, SLE, WN and YF viruses have been reported to trigger apoptosis in host cells (Desprès et al., 1996, 1998; Duarte dos Santos et al., 2000; Jan et al., 2000; Liao et al., 1997; Marianneau et al., 1997, 1998; Parquet et al., 2001, 2002; Prikhod'ko et al., 2001; Su et al., 2002; Xiao et al., 2001; Courageot et al., 2003; Catteau et al., 2003). Apoptosis is an active process of cell death involving a number of distinct morphological changes (Hengartner, 2000; Kimura et al., 2000). Apoptosis is induced via the activation of intracellular signalling systems, a number of which converge on mitochondrial membranes to induce their permeabilization (Hengartner, 2000; Desagher & Martinou, 2000; Ferri & Kroemer, 2001). Members of the Bcl-2 protein family have been shown to exhibit both anti-apoptotic and proapoptotic activities (Adams & Cory, 2001). For example, increased levels of Bcl-2 lead to cell survival whereas excess of Bax is associated with apoptosis (Yang et al., 1997; Jürgensmeier et al., 1998).

The intracellular production of viral proteins has been shown to be essential for the induction of apoptosis by flaviviruses (Desprès et al., 1996; Duarte dos Santos et al., 2000; Prikhod'ko et al., 2001, 2002). However, potent death-promoting activity has yet to be demonstrated for particular DEN proteins. Here, we showed that the DEN M ectodomain can trigger apoptosis in host cells of various origins. Deletion analysis demonstrated that the nine carboxy-terminal amino acids of the DEN M ectodomain were necessary and sufficient for the induction of apoptosis.

	METHODS

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Cell lines and viruses.
Mouse neuroblastoma Neuro 2a and human hepatoma HepG2 cells were cultured as previously described (Duarte dos Santos et al., 2000). The human epithelial 293A cell line was purchased from Quantum Bioprobe. The monkey kidney COS-7 cell line was generously provided by F. Delebecque (Pasteur Institute). The 293A and COS-7 cell lines and the human epithelial HeLa cell line were cultured in DMEM supplemented with 10 % foetal calf serum (FCS) and 2 mM L-glutamine.

The South American strains of DEN-1 virus FGA/89 (GenBank accession no. AF226687) and BR/90 (S64849) have been reported elsewhere (Desprès et al., 1993). DEN-1 virus strains FGA/89 and BR/90, DEN-2 virus strain Jamaica (M20558), DEN-3 virus strain H-87 (NC 001475), DEN-4 virus strain H-241 (NC 002640), JE virus strain Nakayama (JE virus strain SA[V], D90194) and WN virus strain IS-98-ST1 (AF481864) were produced in cultured Aedes pseudoscutellaris AP61 mosquito cells, as previously described (Desprès et al., 1993). YF virus strain 17D-204 Pasteur (X15062) was produced in human SW13 cells (Desprès et al., 1987).

Plasmids.
pCI-neo, pEGFP-N1 and pEYFP-Golgi were purchased from BD Clontech BioSciences. Viral RNA was extracted from purified flavivirus or infected cell lysates using the RNA-plus reagent (Quantum Bioprobe). The RNA was reverse transcribed using the Titan One-Step RT-PCR kit (Roche Molecular Biochemicals) according to the manufacturer's instructions. All constructs were verified by automated sequencing.

The BR/90 cDNA encoding residues C-95 to C-114 (amino acid residues are numbered as for DEN-1 virus; Desprès et al., 1993) was introduced into NheI/SmaI-digested pEGFP-N1, the eukaryotic expression vector containing the gene encoding enhanced green fluorescent protein (EGFP). The resulting plasmid, pC^95–114-EGFP, encodes the prM translocation signal followed by six vector-specified residues, EPPVAT, fused in-frame with the amino terminus of EGFP.

Synthetic oligonucleotide primers containing recognition sites for BsrGI (5' primer) and NotI (3' primer) were used to amplify specific sequences of the flavivirus genome encoding the full-length M ectodomain (residues M-1 to M-74) (Table 1). We constructed pC^95–114-EGFP-M^1–74 by digesting the RT-PCR products with BsrGI and NotI and introducing the resulting fragment into BsrGI/NotI-digested pC^95–114-EGFP, such that the full-length M was directly fused in-frame with the carboxy-terminal end of EGFP. We constructed pC^95–114-EGFP-M^1–40 by amplifying flavivirus cDNAs encoding the M ectodomain (residues M-1 to M-40) by PCR using pC^95–114-EGFP-M^1–74 as a template and a set of 3' primers containing a stop codon (TGA) followed by a NotI restriction site. The PCR products were introduced into pC^95–114-EGFP, such that the flavivirus M ectodomains were produced as fusions with EGFP.

To construct pGalT^1–80-EGFP-M^1–40/DEN-1, a 0·9 kb fragment containing the entire EGFP-M^1–40/DEN-1 fragment was excised from pC^95–114-EGFP-M^1–40/DEN-1 with BamHI and NotI. This fragment was inserted into BamHI/NotI-digested pEYFP-Golgi, such that EGFP-M^1–40/DEN-1 was fused in-frame with the amino-terminal region of -1,4-galactosyltransferase (GalT).

To construct pCR-CD72^1–136, total RNA from the spleens of BALB/cByJRj mice was reverse transcribed to generate cDNA, which was used as template for PCR. An RT-PCR fragment encoding the endodomain followed by the transmembrane domain of mouse CD72 glycoprotein (nt 1–445) was generated, using the following synthetic primers: 5'-TGCTGGAGGAATAGCAGTCTTAAAAATTGGC-3' corresponding to nt 1–31 of the 5' end of the CD72 cDNA and 5'-TATTGGTGGCTTCCCAAATCCTGGTCCCC-3' corresponding to nt 416–445 of the 3' end of the CD72 cDNA. The RT-PCR product was directly inserted into pCR 2.1 TOPO (TOPO TA cloning kit, Invitrogen) according to the manufacturer's instructions to give pCR-CD72^1–136.

We generated pCD72^1–118-EGFP-M^1–40/DEN-1 by amplifying the cDNA encoding the amino-terminal region of CD72 by PCR, using pCR-CD72^1–136 as a template and the following primers: 5'-GAGGCGGCTAGCGCTATGGCTGACGCTATCACG-3' corresponding to the 5' end of the CD72 gene and extended by 11 nucleotides to include a NheI restriction site and 5'-AGACACCCGGGGATAGAGAACTCCCAGGC-3' corresponding to nt 387–402 at the 3' end of the CD72 gene and extended by 14 nucleotides to include a SmaI restriction site. The PCR product was digested with NheI and SmaI and inserted between the NheI and SmaI sites of pC^95–114-EGFP-M^1–40/DEN-1 to generate pCD72^1–118-EGFP-M^1–40/DEN-1.

To construct pC^95–114-EGFP-M^1–40/DEN-1-KDEL, pGalT^1–80-EGFP-M^1–40/DEN-1-KDEL and pCD72^1–118-EGFP-M^1–40/DEN-1-KDEL, PCR fragments containing the DEN-1 M ectodomain (M^1–40/DEN-1) followed by the KDEL motif were generated with the 3' primer 5'-TAAAGCGGCCGCTCACAACTCGTCTTTTGGGTGTCTCAAAGCCCAAGTCTCCAC-3' corresponding to the KDEL sequence and extended by 12 nucleotides to include a stop codon (TGA) followed by a NotI restriction site.

Transient transfection of cells.
Cells were placed in Permanox Lab-Tek chambers (Nalge Nunc International) or six-well plates. After 1 day of culture, cell monolayers were transfected with 6 µg of plasmid per 10⁶ cells in the presence of FuGENE 6 transfection reagent (Roche Molecular Biochemicals), according to the manufacturer's instructions. The fusion proteins were detected by monitoring the autofluorescence of EGFP. Cells were examined under an Axioplan 2 fluorescence microscope (Zeiss). Images were processed on a computer, using RS Image 1.07, Simple PCI 5.1, Adobe Photoshop and PowerPoint software.

Establishment of HepG2 cell clones overexpressing bcl-2.
pZipBcl-2, which contains the sequence encoding human Bcl-2, was generously provided by J. M. Hardwick (Johns Hopkins University, Baltimore, MD, USA). The cDNA encoding human Bcl-2 was inserted into pCI-neo to generate pCI-Bcl-2. We established cell clones that stably produced the Bcl-2 protein by transfecting HepG2 cells with pCI-Bcl-2 in the presence of DOTAP liposomal transfection reagent (Roche Molecular Biochemicals), according to the manufacturer's instructions. The transfected cells were selected on medium containing G418 neomycin (France Biochem). Cell lines stably producing Bcl-2 protein were cloned from single cells by limiting dilution. Western blots were performed with rabbit antiserum directed against the human Bcl-2 protein (kindly provided by R. Mahieux, Pasteur Institute). Indirect immunofluorescence assays were performed with mouse antibodies specific for the human Bcl-2 protein (kindly provided by E. Guillemard, Pasteur Institute).

In situ detection of apoptotic cells.
The cells were fixed by incubation with 3·2 % paraformaldehyde (PFA) in PBS for 20 min. We investigated the nuclear changes associated with apoptotic cell death by incubating fixed cells with 0·1 µg Hoechst 33258 (Sigma) ml^-1 in 0·1 % citrate buffer (pH 6·0) for 10 min at room temperature. Cells were considered to be apoptotic if they exhibited marginated chromatin and nuclear condensation. At least 200 EGFP-expressing cells from three independent cell chambers were used to quantify apoptosis. Apoptosis-induced DNA breaks were detected by the deoxyterminal transferase-mediated dUTP nick-end labelling (TUNEL) method as previously described (Desprès et al., 1996). Nuclear TUNEL assay was performed with Cy3-conjugated streptavidin (Jackson Immunoresearch).

Immunofluorescence.
For immunofluorescence analysis, cells were plated on glass coverslips. Cells were fixed with 3·2 % PFA and permeabilized with 0·1 % Triton X-100 in PBS for 4 min. Rabbit polyclonal antibody to calnexin (SPA-865) was obtained from Stressgen Biotechnologies. Labelling experiments used Cy3-conjugated species anti-IgG antibodies. Cells were observed with an Axiovert 200M fluorescence microscope (Zeiss). Images were processed on a computer, using Simple PCI 5.1, Adobe Photoshop and PowerPoint software.

Flow cytometry analysis of early apoptosis.
Apoptotic assays were carried out by surface staining with the Ca²⁺-dependent phosphatidylserine (PS)-binding protein Annexin V. Transfected HeLa cells were labelled by incubation with Annexin V-APC (BD Pharmingen BioSciences) and 5 µg propidium iodide (PI) (Sigma) ml^-1 in a HEPES-based buffer (140 mM NaCl, 2·5 mM CaCl₂, 10 mM HEPES, pH 7·4) for 15 min on ice according to the manufacturer's instructions. The stained cells were analysed in a FACSCalibur (Becton Dickinson) using CellQuest 3.3 software.

Immunoblotting procedure.
For Western blotting, cell lysates were separated on a 15 % SDS-PAGE gel and then transferred onto a PVDF membrane (Roche Molecular Biochemicals). Membranes were probed with the primary antibody in blocking buffer overnight at 4 °C. Primary antibody binding was detected by incubation with alkaline phosphatase-coupled secondary antibody (BioSys). NBT/BCIP reagents were used to detect bound secondary antibodies.

	RESULTS

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Expression of the M ectodomain leads to apoptosis
To examine the role of M in the induction of apoptosis by DEN-1 virus, we inserted the FGA/89 cDNA encoding the M protein into a mammalian expression vector under the control of the human cytomegalovirus IE promoter. We constructed EGFP-fused M protein by fusing the DEN-1 cDNA gene sequence immediately downstream from the reporter gene encoding EGFP (Fig. 1). The EGFP-fused M proteins contained either the complete M protein, including the both TMDs (residues M-1 to M-74), or only the M ectodomain (residues M-1 to M-40) (Fig. 1). The sequence encoding the internal signal sequence (C^95–114), which is located at the junction of the DEN-1 C and prM proteins and directs the translocation of prM into the lumen of the endoplasmic reticulum (ER) (Chambers et al., 1990; Rice, 1996), was inserted upstream from sequences encoding the EGFP-fused DEN proteins (Fig. 1). The EGFP-fused E proteins including either the stem alone (residues E-392 to E-439) or the stem–anchor region (residues E-392 to E-487) of the E protein served as controls (Fig. 1).

View larger version (27K): [in this window] [in a new window]   Fig. 1. Schematic representation of the EGFP-fused DEN-1 proteins. Fusion proteins consisting of the ER targeting sequence (C95–114, designed SS) of prM, the full-length M (M1–74), the ectodomain (M1–40) of the M protein, the stem–anchor (E392–487) and the stem (E392–487) of the E protein fused to EGFP, are depicted. The transmembrane domain (TMD) is shown. The fusion proteins are not drawn to scale. The names of fusion proteins are indicated on the left.

View larger version (16K): [in this window] [in a new window]   Fig. 2. DEN-1 M ectodomain has proapoptotic properties. HeLa cells were transfected with plasmids encoding the fusion proteins described in Fig. 1. Transiently transfected HeLa cells were harvested after 25 h (A and C) or at the times indicated (B). Fixed cells were stained with Hoechst 33258 (A and B) or assayed by the TUNEL method (C). Fusion proteins were detected by monitoring the autofluorescence of EGFP. Each experimental point represents the mean±SD of results obtained from three separate chambers. Fusion proteins were compared statistically with C95–114-fused EGFP: not significant (n.s., P>0·05) or significant (*P<0·05; **P<0·01; ***P<0·001), according to Fisher and Yates's t-tests. EGFP control (white bar).

Transport of the M ectodomain through the secretory pathway leads to apoptosis
Since the EGFP-M^1–40/DEN-1 fusion (Fig. 1) did not induce apoptosis (Fig. 2A), it appeared that the death-promoting activity of ecto-M was abolished if the prM translocation sequence was deleted. This result suggests that the transport of ecto-M through the secretory pathway plays a key role in the initiation of apoptosis.

To monitor the distribution of ecto-M in relation to cellular organelles possibly involved in induction of apoptosis, we examined the localization of C^95–114-EGFP-M^1–40/DEN-1 and C^95–114-EGFP-M^1–40/DEN-1-KDEL, the latter consisting of the ER retrieval KDEL motif fused to the carboxy-terminal end of the M ectodomain. The KDEL sequence is present in several luminal ER proteins and is recognized by a specific receptor that mediates retrograde transport between the Golgi apparatus and the ER (Pelham, 1996). Immunolabelling experiments revealed extensive colocalization of C^95–114-EGFP-M^1–40/DEN-1-KDEL with the cellular marker for the ER (anti-calnexin) in the perinuclear region, indicating that the ER retrieval sequence promotes the retention of ecto-M within the ER (Fig. 3A, left). In contrast, C^95–114-EGFP-M^1–40/DEN-1 was more dispersed along the secretory pathway. We investigated whether the presence of the M ectodomain in the ER was sufficient to trigger apoptosis by assessing the cytotoxicity of C^95–114-EGFP-M^1–40/DEN-1-KDEL. Expression of KDEL motif-tagged ecto-M did not cause an increase in the number of TUNEL-positive cells relative to the negative control (Fig. 3B), indicating that the ER retrieval sequence may prevent ecto-M-mediated cell death. This finding is consistent with the observation that the presence of the anchor region (C^95–114-EGFP-M^1–74 fusion protein) abolished the death-promoting activity of the M ectodomain (Fig. 2A), possibly by favouring its retention in the ER compartment (Cocquerel et al., 1999).

View larger version (71K): [in this window] [in a new window]   Fig. 3. Subcellular localization of the M ectodomain. Transfected HeLa cells producing fusion proteins were detected by monitoring the autofluorescence of EGFP (A) or analysed for apoptosis (B). (A) EGFP-positive cells were subjected to indirect immunofluorescence staining with anti-calnexin antibodies conjugated to Cy3. Overlap of C95–114-EGFP-M1–40 (M1–40) or C95–114-EGFP-M1–40-KDEL (M1–40-KDEL) with the ER marker is represented by the yellow regions (left). Intracellular distribution of GalT1–80-EGFP-M1–40/DEN-1 (GalT1–80) and CD721–118-EGFP-M1–40/DEN-1 (CD721–118) without (-KDEL) or with (+KDEL) ER retrieval sequence KDEL (right). Scale bar, 10 µm. (B) Nuclear DNA nicks of transfected cells were monitored by the TUNEL assay after 30 h of transfection. C95–114-EGFP, GalT1–80-EGFP and CD721–118-EGFP served as negative controls (white bars). Fusion proteins were compared statistically with their respective negative controls as described in the legend to Fig. 2: not significant (n.s., P>0·05) or significant (*P<0·05; **P<0·01; ***P<0·001).

Thus, our studies at this point suggested that the exit of ecto-M from the Golgi apparatus was required for the induction of apoptosis. To investigate this issue, we engineered a fusion protein, CD72^1–118-EGFP-M^1–40/DEN-1, containing the cytosolic tail of a type II integral membrane glycoprotein, CD72 (Ying et al., 1995), in place of the ER targeting signal of prM. Residues CD72¹ to CD72¹¹⁸ encompass the membrane-anchoring signal peptide that targets the glycoprotein to the plasma membrane (PM). The PM, and to a lesser extent the Golgi apparatus, was clearly labelled in transfected HeLa cells producing CD72^1–118-EGFP, indicating that the CD72 translocation signal mediates the engagement of a transport pathway at the cell surface (data not shown). Both the Golgi apparatus and the cell surface were clearly labelled in HeLa cells producing CD72^1–118-EGFP-M^1–40/DEN-1, whereas only the ER was stained in HeLa cells producing CD72^1–118-EGFP-M^1–40/DEN-1-KDEL (Fig. 3A, right). Upon transfection with pCD72^1–118-EGFP-M^1–40/DEN-1, we observed apoptotic nuclear fragmentation in more than 15 % of fusion protein-expressing HeLa cells after 30 h of transfection (Fig. 3B). In contrast, production of CD72^1–118-EGFP or CD72^1–118-EGFP-M^1–40/DEN-1-KDEL did not result in cell death. Taken together, these results suggest that the export of ecto-M from the Golgi apparatus to the plasma membrane is essential for the initiation of apoptosis. Replacement of the prM translocation sequence by the CD72 membrane-anchoring signal peptide preserved the death-mediating activity of EGFP-fused M^1–40/DEN-1 (Fig. 3B). Thus, ecto-M may exert its cytotoxic effects by activating an apoptotic signalling pathway that does not require a soluble form.

The M ectodomains of JE, WN and YF viruses have proapoptotic properties
As the DEN-1 M ectodomain induced apoptosis, we investigated whether the M ectodomains of other DEN virus serotypes and of other apoptosis-inducing flaviviruses, such as wild-type strains of JE, WN and YF viruses, also cause cell death. Production of the various EGFP-fused M ectodomains was confirmed by Western blotting (data not shown). All flavivirus M ectodomains induced apoptosis after 25 h of transfection (Fig. 4A), suggesting that the proapoptotic properties of ecto-M are conserved among apoptosis-inducing flaviviruses. The M ectodomains of DEN-1 and DEN-2 viruses were the most potent inducers of apoptosis.

View larger version (16K): [in this window] [in a new window]   Fig. 4. The M ectodomains from apoptosis-inducing flaviviruses have proapoptotic properties. HeLa cells were transfected with constructs encoding C95–114-EGFP (control, white bar), C95–114-EGFP-M1–40/DEN-1 (DEN-1), C95–114-EGFP-M1–40/DEN-2 (DEN-2), C95–114-EGFP-M1–40/DEN-3 (DEN-3), C95–114-EGFP-M1–40/DEN-4 (DEN-4), C95–114-EGFP-M1–40/JE (JE), C95–114-EGFP-M1–40/WN (WN) or C95–114-EGFP-M1–40/YF.wt (YF) (A), or with plasmids encoding C95–114-EGFP (control, white bar), C95–114-EGFP-M1–40/YF.wt (M1–40/YF.wt) or C95–114-EGFP-M1–40/YF.17D (M1–40/YF.17D) (B). Transfected HeLa cells were stained with Hoechst 33258 after 25 h of transfection and examined for changes in nuclear morphology. Fusion proteins were compared statistically with their respective controls as described in the legend to Fig. 2: not significant (n.s., P>0·05) or significant (*P<0·05; **P<0·01; ***P<0·001).

The DEN M ectodomains induce apoptosis in tumour and transformed cells
As DEN virus induces apoptosis in mouse neuroblastoma Neuro 2a and human hepatoma HepG2 cells (Desprès et al., 1996; Duarte dos Santos et al., 2000; Jan et al., 2000; Lin et al., 2000; Marianneau et al., 1997; Su et al., 2001), we tested the ability of the DEN M ectodomain to cause death in these susceptible cell lines. We showed that transfected Neuro 2a cells and HepG2 cells producing C^95–114-EGFP-M^1–40/DEN-1 or C^95–114-EGFP-M^1–40/DEN-2 underwent apoptosis after 30 h of transfection (Fig. 5), suggesting that DEN ecto-M induces apoptosis in tumour cells of various origins.

View larger version (23K): [in this window] [in a new window]   Fig. 5. The DEN M ectodomain induces apoptosis in cells of various origins. Tumoral Neuro 2a and HepG2 cell lines and transformed 293A and COS-7 cell lines were transfected with plasmids encoding C95–114-EGFP-M1–40/DEN-1 (hatched bar) or C95–114-EGFP-M1–40/DEN-2 (grey bar). Transfected cells were stained with Hoechst 33258 and examined for chromatin condensation. The percentages of fusion protein-expressing cells with apoptotic nuclei after 30 h of transfection are indicated. Fusion proteins were compared statistically with C95–114-fused EGFP (white bar) as described in the legend to Fig. 2: not significant (n.s., P>0·05) or significant (*P<0·05; **P<0·01; ***P<0·001).

The apoptotic effect of the M ectodomain is blocked by Bcl-2
We investigated whether the overexpression of Bcl-2 protected HepG2 cells against the apoptotic effects of M^1–40/DEN-2 by establishing permanent HepG2 cell lines that stably overexpressed human Bcl-2, by transfection with pCI-Bcl-2. Western blot analysis (Fig. 6A) and an indirect immunofluorescence assay (Fig. 6B) showed that HepG2/bcl-2#5, a clone stably expressing bcl-2, overproduced human bcl-2. In these experiments, the HepG2/neo#1 cell clone served as a negative control. Comparison of HepG2/bcl-2#5 cells with HepG2/neo#1 cells showed that the overexpression of Bcl-2 did not affect the intracellular synthesis of the fusion proteins in transfected cells (data not shown). We then investigated the effect of bcl-2 on M^1–40/DEN-2-induced apoptosis by monitoring changes in nuclear morphology (Fig. 6C). After 30 h of transfection, 7 % of M^1–40/DEN-2-expressing HepG2/neo#1 cells underwent apoptosis. In contrast, less than 2 % of M^1–40/DEN-2-expressing HepG2/bcl-2#5 cells were apoptotic at this time. After 48 h of transfection, M^1–40/DEN-2-expressing cells were still detected among transfected HepG2/bcl-2#5 cells (data not shown). Thus, M ectodomain-induced apoptosis is inhibited by overexpression of Bcl-2.

View larger version (26K): [in this window] [in a new window]   Fig. 6. Overproduction of bcl-2 protects HepG2 cells against the proapoptotic effects of the DEN-2 M ectodomain. The overproduction of bcl-2 in HepG2 cell clones was assessed by Western blotting (A) and indirect immunofluorescence (B) assays, using antibodies specific for the human Bcl-2 protein. (C) HepG2/bcl-2#5 and HepG2/neo#1 cells were transfected with plasmids encoding C95–114-EGFP (control, white bar) or C95–114-EGFP-M1–40/DEN-2 (hatched bar). After 30 h of transfection, transiently transfected cells were stained with Hoechst 33258 and examined for chromatin condensation. Fusion protein was compared statistically with C95–114-fused EGFP as described in the legend to Fig. 2: not significant (n.s., P>0·05) or significant (*P<0·05; **P<0·01; ***P<0·001).

View larger version (27K): [in this window] [in a new window]   Fig. 7. The carboxy-terminal amino acids of the M ectodomain constitute a proapoptotic sequence. Transfected HeLa cells were assayed for apoptotic nuclear fragmentation after 25 h of transfection (B) or for the early stage of apoptosis after 20 h (C). (A) Amino acid sequence alignments for mutant proteins, the names of which are shown on the right. (B) HeLa cells were stained with Hoescht 33258 and examined for chromatin condensation. C95–114-fused EGFP (control, white bar) served as a negative control. Statistical analysis for fusion proteins was carried out by comparison with the control as described in the legend to Fig. 2: not significant (n.s., P>0·05) or significant (*P<0·05; **P<0·01; ***P<0·001). (C) The rate of early apoptosis was analysed by Annexin V binding, as assessed by flow cytometry analysis. Apoptosis in fusion protein-expressing HeLa cells was defined as EGFP-positive cells that bound Annexin V-APC but excluded propidium iodide (PI). For each sample, data from 10 000 EGFP-positive cells were collected. The percentages of M1–40- and M32–40-expressing cells labelled with Annexin V are indicated (inset squares).

We investigated whether the nine residue sequence of the DEN-2 ecto-M is potent in triggering apoptosis by introducing the substitutions R³⁴T, F³⁶I, V³⁷L and N³⁹H into the EGFP-fused M^{1–40/YF.17D} that had lost its cytotoxicity (Fig. 8A). In transfected HeLa cells, expression of mutant protein C^95–114-EGFP-M^{1–40/YF.17D} (T³⁴, I³⁶, L³⁷, H³⁹) resulted in cell death (Fig. 8B), indicating that residues M-34, M-36, M-37 and M-39 are critical for induction of apoptosis by ecto-M. We evaluated the effect of the F³⁶ mutation on the death-promoting activity of DEN ecto-M by generating a fusion protein, C^95–114-EGFP-M^1–40/DEN-2 (F³⁶), with a phenylalanine residue in position 36 of the DEN-2 M ectodomain (Fig. 8A). In transfected HeLa cells, the resulting mutant protein C^95–114-EGFP-M^1–40/DEN-2 (F³⁶) induced apoptosis less efficiently than the parental fusion protein (Fig. 8B). Thus, the overall apoptosis-inducing activity of the M ectodomain reflected the intrinsic proapoptotic properties of residues M-32 to M-40 and the substitution of a leucine (YF ecto-M) or an isoleucine (DEN-2 ecto-M) for the phenylalanine in position M-36 can affect these properties.

View larger version (20K): [in this window] [in a new window]   Fig. 8. Residues M-34 to M-39 contribute to the death-promoting activity of the M ectodomain. (A) Amino acid sequence alignments of M1–40/YF.17D, M1–40/DEN-2 and mutants M1–40/YF.17D (T34, I36, L37, H39) and M1–40/DEN-2 (F36). Identical amino acids are indicated (*). (B) After 25 h of transfection, fusion protein-expressing HeLa cells were stained with Hoechst 33258 and examined for chromatin condensation. Fusion proteins were compared statistically with C95–114-fused EGFP (control, white bar) as described in the legend to Fig. 2: not significant (n.s., P>0·05) or significant (*P<0·05; **P<0·01; ***P<0·001).

	DISCUSSION

TOP ABSTRACT INTRODUCTION METHODS RESULTS DISCUSSION REFERENCES

The M ectodomains of wild-type strains of JE, WN and YF viruses also have proapoptotic properties, suggesting that the 40 amino acid ectodomain of M may play an important role in flavivirus-induced cytopathic effects. Viscerotropic YF virus causes damage to liver cells in humans and hepatocytic apoptosis has been observed in infected livers (Marianneau et al., 1998; Xiao et al., 2001). Two live attenuated vaccine strains, 17D and French neurotropic virus (FNV), are known to have lost the ability to cause viscerotropic disease (Wang et al., 1995). Little is known about the molecular determinants of virulence in wild-type YF virus. Interestingly, all YF vaccine strains studied to date include a common amino acid leucine to phenylalanine substitution at position M-36 (Monath, 1999; Hahn et al., 1987). We found that this substitution abolishes the death-inducing activity of the YF M ectodomain, suggesting that residue M-36 may play a crucial role in the attenuation of viscerotropic YF virus. Mutant YF viruses produced by infectious clone technology will elucidate the potential role of residue M-36 in YF virus pathogenicity. The I³⁶F substitution results in a reduction of the cytotoxicity of the DEN-2 M ectodomain. Thus, residue M-36 may be essential for the efficient induction of apoptosis by the DEN and YF M ectodomains.

Transformed human 293A cells were resistant to the apoptotic effects mediated by the M ectodomain. The embryonic kidney 293A cell line expresses the Ad5 E1A and E1B genes (Louis et al., 1997). The transforming activities of these genes are based on their ability to interact with the transcription factor p53, which is the central component in a complex network of apoptotic-signalling pathways (Burns & El-Deiry, 1999; White, 2001). The viral oncogene E1B encodes two proteins, E1B 55K and E1B 19K, which block intracellular signalling as part of p53-dependent proapoptotic pathways (White, 2001). COS-7 cells, which undergo apoptosis in response to M ectodomain production, possess an anti-apoptosis activity independent of p53 activity (Tsai et al., 2000). The cellular concentration of p53, one of the target genes for NF-B, has been reported to increase during the early stages of DEN virus infection (Jan et al., 2000). We have undertaken experiments to determine whether the death-promoting activity of the M ectodomain requires p53 activation.

Apoptosis induced by flavivirus infection is efficiently prevented by the anti-apoptosis protein Bcl-2 (Liao et al., 1997, 1998; Su et al., 2001). The overexpression of Bcl-2 also protected HepG2 cells against the death-promoting activity of the M ectodomain. Bcl-2 probably regulates apoptosis by controlling the export of mitochondrial cytochrome c and caspase activation (Adams & Cory, 2001; Desagher & Martinou, 2000). It has been suggested that the overproduction of Bcl-2 or of the Ad5 E1B 19K protein, a functional homologue of Bcl-2, prevents apoptosis by modulating the activities of the proapoptotic factor Bax, which is induced by p53 (Lomonosova et al., 2002). Bax is located predominantly in the cytosol, but is translocated to the mitochondria early in apoptosis, leading to the release of apoptogenic factors (Adams & Cory, 2001; Kuwana et al., 2002). A steady increase in the amount of Bax has been reported to occur in response to flavivirus infection (Parquet et al., 2001, 2002). It is therefore of great interest to consider the role of the factor Bax in apoptosis induced by the M ectodomain.

In summary, we have provided evidence that a nine residue sequence designated ApoptoM is directly involved in induction of apoptosis by the M protein. This finding raises the question of whether initiation of apoptosis may result from the interaction of ApoptoM with organelle-specific signalling molecules that elicit death pathways (Ferri & Kroemer, 2001). Such interaction might occur at the same time as the prM precursor glycoprotein is processed in the exocytotic pathway of the trans-Golgi network, resulting in M and a ‘pr’ fragment. Although M is not normally known to undergo proteolysis, an alternative explanation is that apoptosis-signalling pathways are activated through mechanisms that involve cleavage of ApoptoM from the M ectodomain during transport in the late secretory pathway.

The data presented here suggest an important role for the small M protein in flavivirus-induced apoptosis. During the late stage of apoptosis, the plasma membrane disassembles into membrane-enclosed vesicles (apoptotic bodies) that are generally eliminated by macrophage-like cells. The mechanisms of host defence involving phagocytosis of apoptotic bodies associated with the production of cytokines may cause local tissue injury. Our future experiments will assess the role of ApoptoM in the pathophysiological manifestations consecutive to flavivirus infection.

	ACKNOWLEDGEMENTS

 
We would like to thank S. Vigneau and J.-F. Bureau for the CD72 constructs, P. Marianneau for the HepG2/bcl-2 cell clones and S. Davison for the mutant proteins. We thank M.-P. Frenkiel and M.-T. Drouet for technical expertise. We thank J. M. Hardwick (Johns Hopkins University, Baltimore, MD, USA), M.-L. Gougeon, H. Lecoeur and F. Pénin (IBCP, Lyon) for helpful comments. We would also like to thank S. Shorte, E. Perret and P. Roux (Centre d'Imagerie Dynamique, Pasteur Institute, Paris) for assistance with microscopy. This research was supported by grants from the Direction Générale de l'Armement (DSP/STTC, program 99.34.031) and from the Pasteur Institute (Transverse Research Program 21 and Direction de la Valorisation et des Partenariats Industriels). A. C. is funded by a scholarship from the French Ministry of Education, Research and Technology.

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Received 13 February 2003; accepted 21 May 2003.

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