¹Department of Viral and Cellular Molecular Genetics, Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia

Corresponding author:Igor A. Grivennikov,Department of Viral and Cellular Molecular Genetics, Institute of Molecular Genetics, Russian Academy of Sciences, Kurchatov Sq. 2, 123182 Moscow, Russia. Tel: (+7-499)-1960014; Fax: (+7-499)-1960221; E-mail: igorag@img.ras.ru.

	ABSTRACT
	INTRODUCTION
	METHODS
	RESULTS
	DISCUSSION
	ACKNOWLEDGEMENTS
	REFERENCES

	ABSTRACT

    To examine the effects of the tat and nef regulatory genes of human immunodeficiency virus (HIV-1) on cell differentiation we used the mouse embryonic stem cells (ESC) as a model. Proliferation, embryoid bodies (EB) formation and subsequent differentiation into cardiomyocytes, glial and neuronal cells were investigated in ESC lines transfected with these genes. It has been shown that the transfection of ESC by the tat gene increased their proliferating activity, whereas the nef genetransfected ESC showed its decrease. The number of embryoid bodies formed was higher in the cultures of ESC transfected by the nef and lower in the cells transfected by the tat in comparison with controls. The percentage of embryoid bodies with contracting cardiomyocytes was higher against control in the nef transfected cells and lower in ESC transfected with the tat. There were no reliable differences in the appearance of glial cells between control and the nef and tat transfected cell lines. Spontaneous differentiation of ESC into neuronal cells was almost not observed in the nef transfected cells, in contrast to control and the tat transfected cells. However, addition of retinoic acid (RA) to the nef transfected cells caused even a slight increase in neuron formation as compared to control ESC treated with RA. Thus, for the first time we have shown that the tat and nef regulatory genes of HIV-1 had a visible effect on proliferation of ESC and some first steps of their differentiation. In general, the reverse correlation between the effects of these two viral genes on ESC proliferation and differentiation were observed.

	INTRODUCTION

    Studies on functional anatomy of human immunodeficiency virus (HIV) genome is one of approaches to understanding fine mechanisms of the viral interaction with cells. To fully understand functions of particular viral genes, it seems useful to investigate not only their effect on HIV sensitive human cells but also on other cell types and on cells of other species. In this respect, murine embryonic stem cells (ESC) might be a convenient model allowing one to study the impact of particular HIV genes also on the very early stages of differentiation processes. This point hasn’t yet been studied in detail, although there is some evidence of HIV and some of its genes interference with differentiation of various cell types (1, 2, 3).

    Pluripotent ESC is often used as a model for the study of differentiation processes. These cells retain the ability to differentiate both in vitro system and after introduction in blastocytes (4). One of the main features of ESC in vitro is their ability to differentiate into embryoid bodies (EBs) under specific culture condition. ESC differentiation can be either spontaneous or induced by some chemical compounds and growth factors. It is well known that activin A and transforming growth factor beta-1 (TGFβ-1) induce the mesodermal cell differentiation into cardiomyocytes and skeletal muscle cells. The factors of another group – retinoic acid, fibroblast growth factor (FGF) and epidermal growth factor (EGF) induce a direct differentiation of ESC to mesodermal and ectodermal cells.  Finally, nerve growth factor (NGF) and hepatocyte growth factor (HGF) are involved in the development of all three embryonic germ layers: their action causes the formation of liver, pancreas, muscular, hematopoietic and neuronal cells (5, 6, 7). Genetic control studies of the myogenic and epithelial differentiation of ESC under the action of some growth factors in vitro showed that the expression of tissue-specific genes was the same as in the normal developmental process (5, 8).

    The another way to change proliferation and differentiation of ESC is connected to their genetic modification by the genetic vectors containing some cellular genes. It has been shown, for example, that overexpression of telomerase in ESC confers growth advantage, stress resistance, and enhanced differentiation of these cells towards the hematopoietic lineage (9).

    Thus, ESC is a convenient test-system for the investigation of the effects of different genes on the processes of the cell differentiation. The present study is undertaken to investigate the effects of  the HIV-1 tat and nef genes on the proliferation and differentiation of ESC. The function these accessory of viral genes is studied for a long time.

    Tat protein is expressed early in the viral life cycle and stimulates viral gene expression by interacting with the TAR element found in HIV mRNA (10). Tat has been shown to bind several intracellular and extracellular proteins which suggests that it is capable of modulating various biological effects. Nef protein is an HIV-1 virulence factor shown to promote viral pathogenicity by altering host cell signaling pathways (11, 12). This protein contributes to the replication of primate lentiviruses by altering the trafficking of cellular proteins involved in adaptive immunity (class I and II major histocompatibility complex) and viral transmission (CD4 and DC-SIGN).

    There are a lot of data that demonstrate Tat and Nef effects on cellular metabolism. It has been shown that these regulatory proteins can be influenced by the process off proliferation (13, 14, 15, 16, 17) apoptosis (18, 19) cancerogenesis (17, 20, 21) sensitivity cells to ionizing radiation (22) neurotoxicity (23) and some others.

    The study of HIV regulatory genes attaching the cells which are nonpermissive for the virus is a way to estimate the universality of these genes action on metabolic processes in animal cells. The use of pluripotent embryonic stem cells for this purpose also allows  to investigate the influence of the viral genes not only on the cell proliferation but on cellular differentiation as well.

    The goal of this work is to study the effect of these viral regulatory genes on ESC proliferation, EBs formation and their differentiation in cardiomyocytes, neuronal and glial cells in vitro.

	MATERIALS AND METHODS

Growth of ESC and embryonic fibroblasts
     Mouse R1 line ES? (kindly presented by Dr. A. Nagy, Mount Sinai Hospital, Canada) was isolated from agouti-color (129/Sv × 129/SvJ) F1 line mouse blastocytes (24).  R1 line of ESC was routinely maintained at 37°C humidified air with 5% CO2  in alfa-MEM medium containing 15% fetal bovine serum (FBS) (“Gibco”, USA), 0.1 mM 2-mercaptoethanol, 2 mM L-glutamine, nonessential amino acids (“Gibco”, USA), nucleosides (“Sigma”, USA), vitamins (“ICN”, USA) and gentamycin (20 mg/ml). As a nutrient (feeder) layer for ESC, primary fibroblasts from 11-12 day-old embryo mice whose proliferation had been blocked by mitomycin C (5 μg/ml) were used. DMEM (“Sigma”, USA), containing 10% of FBS and all above mentioned additions except 2-mercaptoethanol, was used as the growth medium for the primary culture of fibroblasts. When ESC were cultivated without feeder, LIF (leukemia-inhibiting factor) (“Sigma”, USA) at a concentration of 10 ng/ml was added to the medium to block spontaneous differentiation of these cells (25). Cell replating accompanied by medium changing was repeated every three day.

Recombinant plasmids
     Mouse R1 line ES? (kindly presented by Dr. A. Nagy, Mount Sinai Hospital, Canada) was isolated from agouti-color (129/Sv × 129/SvJ) F1 line mouse blastocytes (24).  R1 line of ESC was routinely maintained at 37°C humidified air with 5% CO2  in alfa-MEM medium containing 15% fetal bovine serum (FBS) (“Gibco”, USA), 0.1 mM 2-mercaptoethanol, 2 mM L-glutamine, nonessential amino acids (“Gibco”, USA), nucleosides (“Sigma”, USA), vitamins (“ICN”, USA) and gentamycin (20 mg/ml). As a nutrient (feeder) layer for ESC, primary fibroblasts from 11-12 day-old embryo mice whose proliferation had been blocked by mitomycin C (5 mg/ml) were used. DMEM (“Sigma”, USA), containing 10% of FBS and all above mentioned additions except 2-mercaptoethanol, was used as the growth medium for the primary culture of fibroblasts. When ESC were cultivated without feeder, LIF (leukemia-inhibiting factor) (“Sigma”, USA) at a concentration of 10 ng/ml was added to the medium to block spontaneous differentiation of these cells (25). Cell replating accompanied by medium changing was repeated every three day.

Recombinant plasmids
     Plasmid pNEF containing the nef gene of HIV-1 HXB3 isolate (the HindIII/TaqI-fragment, nucleotides from 8306 to 8998) under the control of cytomegalovirus (CMV) promoter was generously supplied by Dr. Hammes (26).  To construct a HIV gene tat-carrying plasmid, the SalI/PstI fragment (from nucleotide 5786 through to the 3’ end) of HXB2 isolate with the deleted gene nef-carrying region (the BamHI/BgIII fragment, nucleotides 8475 to 9558) was used. The Sal1/Pst1 fragment containing 2^nd and 3^d exons (the 1^st and the 2^nd translated exons, respectively) of the gene tat and the polyadenylation signal on its own was cloned after blunting the ends in the expression vector pcDNA3 (“Invitrogen”, USA) at the EcoRV site. The obtained plasmid, pTat-neo, carried the gene of resistance to neomycin and contained gene tat under CMV promoter. Recombinant plasmids were purified by standard method (27).
     To produce ESC transfected by the eGFP gene, we used the plasmid pEGFP-C1 (“Clontech”, USA, No 6084-1) carrying this gene under the control of CMV promoter. eGFP-transfected cells were observed under a fluorescence microscope  Axioskop 2 plus (“Carl Zeiss”, Germany).

Cell transfection and selection
     ESC transfection by the vectors containing the tat or nef genes was performed by electroporation on “SUM-4” electroporator (Institute of Molecular Biology RAS, Moscow, Russia) under the following specially selected conditions: impulse duration, 1.5 ms; power, 400 W. 10 μg of plasmid DNA was used for the transfection of 1,000,000 cells. To reveal transfectants with the nef gene, co-transfection of pNef plasmid with plasmid pSV2neo (kindly presented by Dr. Southern P.J.) at a ratio of 10:1 was performed. ESC were transfected also by plasmid pSV2neo or pcDNA3 alone and used as a control. The selection of transfected cells in both cases was performed using G418 (200 μm/ml). The frequency of transfection was near 2 × 10^-4. Polyclonal cultures were used in all further experiments. Every three months additional selection with G418 was performed for all transfected cell cultures to prevent the appearence the cells without transgenes.

The presence of the nef and tat gene transcriptsin transfected cells was analyzed by RT- PCR with “Access RT-PCR System” (“Promega”, USA). The following primers were used:
forthe nef - 5’-GGTGGCAAGTGGTCAAAAAGTAGTG-3’, 5’-AATCAGGGAAGTAGCCTTGTGTGTG-3’
for the tat - 5’-GAGCCAGTAGATCCTAGACTAGAGC-3’, 5’-TCTGATGAGCTCTTCGTCGCTGTC-3’

    Conditions for PCR were the following: 94°C 48 s., 59°C 30 s, 72°C 1 min., 27-30 cycles, then 72°C 7-10 min. The predicted sizes of amplicons were: for the tat - 177 bp, for the nef - 367 bp.

Assay for cell proliferation
     An assessment of the proliferative activity of control and transfected ESC lines was carried out by the cytochemical method using MTT (3-(4,5-dimethyl tiasole-2-il)-2,5-diphenyl tetrasolium bromide) as previously described (28). At the same time, the number of alive cells used in the experiments was evaluated by Trypan Blue exclusion test under the inverted microscope Olympus CKX41 (“Olympus”, Japan) in a hematocytometer. The results were taken on the 3d day after the cell plating.

EBs formation and cardiomyocyte differentiation
     To perform the differentiation of ESC into EB, ESC was separated from fibroblast feeder. For this purpose, the cells were treated with trypsin (0.05%, 5 min) and obtained cell suspension were preplated on Petri dish (“Nunc” Denmark, d = 60 mm) during 15 min at 37°C, 5% CO2. This time was sufficient for the main mass of fibroblasts to get attached to the bottom of the plate, whereas ESC was stayed in the suspension. Cells from the suspension were pelleted by centrifugation, and viable cell numbers were determined. The frequency of contaminating embryonic fibroblasts in the undifferentiated (day 0) ESC samples was estimated to be less than 0.2% based on cell size during counting. To form EBs, suspension of ESC (1000 cells per well) was transferred to 96-U plates (“Nunc” Denmark) and then they were placed in CO2-incubator (5% CO2). After 3 days the formed EBs were counted in 10 wells for each cell line. The quantities of the beating clusters of cardiomyocytes in the plates were counted during 3 weeks of the incubation under the inverted microscope Olympus CKX41 (“Olympus”, Japan). Each experiment was repeated at least 4 times.

Neuronal and glial differentiation
     EBs obtained from ESC were incubated for 2 days in the culture medium containing 1 μM of retinoic acid and then seeded by 8-10 EBs per well on gelatin (0.01%) coated 24 well plates (“Nunc” Denmark). The same quantities of EBs were incubated without retinoic acid and served as a control. Plates were placed in CO2-incubator (5% CO2) for differentiation for 20 days. Half of the culture medium was changed every 3 days. To detect different types of ESC differentiation, 10 days later part of the plates were processed for immunocytochemistry with antibodies raised against  nestin, an antigen for neuronal precursor cells (“Chemicon”, USA) and GFAP (glial fibrillary acidic protein) (“Sigma”, USA). The remaining plates were incubated for additional 10 days to obtain neuronal differentiation which was detected with antibodies to MAP2 (mature neuronal phenotype) (“Sigma”, USA). To obtain quantitative characterization of neuronal differentiation of transfected cells the experiments were performed as follow. 8-10 EBs obtained from each of the cell line were transferred to the well of 24-well plate and after 10 days (for nestin) and 20 days (for MAP2) of incubation the quantities of nestin- and MAP2-positive cells were determined in each  well using the microscope Olympus CKX41 (“Olympus”, Japan), as described below (see “Materials and Methods”, Immunocytochemistry). Ten wells for each cell line were counted.

Tests on pluripotency of transfected ESC

    Alkaline phosphatase detection.ESC was plated onto cover glasses with a mitomycin-blocked fibroblast feeder. After one day of cultivation, the cells were fixed by cooled acetone (+4°C) for 1 min, air dried and then incubated in a solution of AS-B1-phosphate and BB-blue dye at 37°C for 1 h (29). The stained cell preparations were studied under the microscope, and cells producing a positive response to alkaline phosphatase activity were regarded as non-differentiated.

    SSEA-1 detection.The colonies of ESC grown on fibroblast feeder were washed two times with PBS and fixed in 100% methanol (-20°?, 5 min). Then cells were washed two times by PBS-0.01% Tween-20 and nonspecific binding was blocked by PBS-0.01% Tween-20 solution containing 5% of dry milk (solution A) and 15% FBS at room temperature for 30 min. Cells were incubated with anti-SSEA-1 mouse monoclonal antibodies (1:10 in solution A) for 1 h at room temperature. After 3 times washing with PBS-0.01% Tween-20 the secondary Alexa Fluor® 546 goat anti-mouse IgG (H+L) (1:1000) from “Molecular Probes” (USA) in PBS-0.01% Tween-20 were added for additional 1 h. After incubation at room temperature samples were washed 3 times with PBS-0.01% Tween-20 and investigated under Axioskop 2 plus microscope (“Carl Zeiss”, Germany).

Immunocytochemistry
    The cells generated from EBs were fixed with freshly prepared 4% formaldehyde in PBS during 30 min. After 4-time washing with PBS, cells were incubated in PBS with 0.1% Triton X-100 and 2-5% of FBS (solution B) during 15 min. Then the samples were incubated with the first specific antibodies (anti-nestin 1:500, anti-GFAP 1:100, anti-MAP2 1:500) overnight at +4°C. Next day antibodies were removed by three times washing with solution B and incubated at room temperature for additional 2 h with biotinylated secondary antibodies against mouse immunoglobulins (1:500; “IMTEK”, Russia). After three times washing with solution B streptavidin conjugated with peroxidase (1:100; “IMTEK”, Russia) was added for 1 h. After the incubation and washing (three times with solution B) colour was developed with 3-amino-9-ethylcarbazole (“Sigma”, USA). The detection of stained cells in cultures was performed using the microscope Olympus CKX41 (“Olympus”, Japan).

Statistical analysis
    All statistical analyses were performed using the “Sigma Plot” software package (“Jandel Scientific Corp.”, USA). Results are expressed as mean ?SEM. Differences between groups of data were analyzed by one-way analysis of variance (one-way ANOVA). Statistical significance was accepted if p < 0.05.

	RESULTS

Gene expression under CMV promoter
     The efficiency assessment of the CMV promoter for transgene expression in ESC line R1 was conducted at the first stage of our work. The necessity of this kind of experiment was started in light of a study showing weaker activity of the CMV promoter in ESC lines D3 and J1, as compared with to CBA and EF promoters (30).  The results of our experiments (Fig.1) showed that the expression of EGFP gene under the control of the CMV promoter in R1 line of ESC was efficient.
The data obtained allowed us to take under the experiments on the ESC transfection by constructs with the regulatory tat and nef genes of HIV-1 under the control of the CMV promoter.

View larger version : [in a new window] Figure 1. EGFP expression in ESC transfected by a plasmid carrying the eGFP gene under the control of CMV promoter. a, colonies of ESC in a light microscope; b, the same colonies in a fluorescent microscope; magnification  ×200.

View larger version : [in a new window] Figure 2. tat and nef genes expression assessed by RT-PCR. Lanes 1,3, cell line es-neok (negative control), lane 2, cell line es-tat, lane 4, cell line es-nef.

Characterization of transfected cell lines
     After the transfection of ESC and subsequent selection four different cell lines were obtained:  es-neok (transfected by plasmid pSV2neo, control), es-pcDNA3 (transfected by pcDNA3, control), es-tat (transfected by plasmid pTatneo) and es-nef (transfected by plasmids pNef and pSV2neo).  By RT-PCR expression of the tat gene in es-tat cells and the nef gene in es-nef cells was detected (Fig. 2).
     No changes in morphology were observed in each of the four ESC lines. The alkaline phosphatase and SSEA-1 staining served as markers of the mammalian ESC pluripotent status (25, 30, 31, 32). All the obtained cell lines had the same level of staining of these markers (Fig. 3 and 4).
    Although the expression of the nef gene in the es-nef cell line was easily detected in the first passages, it was entirely lost at later passages. This result is in agreement with the data obtained earlier and the observation that it is difficult to establish stable cell lines constitutively expressing Nef due to its toxicity in transfected cells (33, 34)

View larger version : [in a new window] Figure 3.  Immunofluorescent detection of SSEA -1 expression in transfected ESC lines. a, es-neok (control);  b, es-tat;  c, es-nef; magnification  ×200.

View larger version : [in a new window] Figure 4. Detection of alkaline phosphatase in transfected ESC growing on fibroblast feeder cells. a, colonies of es-nef, stained; b, fibroblast feeder cells, not stained (date for es-neok and es-tat not shown);   magnification ×200.

Influence of the tat and nef genes on proliferation of ESC
     Differences between the lines of ESC transfected by the tat and nef were brought to light when studying their proliferating activity. As follows from the results presented in Fig. 5, ESC proliferation in the es-tat cell line (black column) was about 20% higher and in the es-nef cell line (gray column) was about 20% lower compared to the es-pcDNA3 and es-neok control (white column) cell lines respectively.
    There were no reliable differences in proliferative activity between control cell lines es-neok and es-pcDNA3 in our experiments. The results with only es-neok line are presented in Fig. 5. Transfection of the plasmid containing the tat gene under the control of metallotioneine promoter (16, 17) led to the same effect (data not shown).

View larger version : [in a new window] Figure 5. The effect of HIV-1 regulatory genes tat and nef on the proliferation of transfected ESC: white column - es-neok (control), black column - es-tat, gray column - es-nef. *, ?<0,05, n = 20.

Influence of tat and nef genes on EBs formation and their differentiation into cardiomyocytes
    The next stage of our work was the investigation of the effect of tat and nef genes on spontaneous formation of EBs in vitro. EBs derived from ESC involves many events of early embryonic development. The analysis of spontaneous differentiation showed that EBs was formed after 2 or 3 days of ESC plating in the absence of the feeder cells. When EBs was transferred onto gelatin coated 4 well plates it was attached to the substrate so that the migration of the cells from the EBs and their differentiation into the cells of different types were observed. Our experiments allowed to see that the efficiency of EBs formation in R1 cell line was dependent on the number of cells, seeded on the feeder-free surface of the plate and the cultivation time of EBs before the beginning of differentiation.
    After 5-6 days of EBs attachment to the surface, spontaneously contracting cardiomyocyte cells were observed. The time of cardiomyocyte development in vitro varied from 7 to 20 days after cell plating. The pulsation frequency of these cells was also variable and dependent on cultivation time of EBs. The frequency did not exceed 60 contractions per minute during the first day and slowly decreased eventually.
    When analyzing a possible effect of tat and nef genes on ESC differentiation, experiments were conducted to estimate the following parameters for all cell lines: 1) time needed for EBs formation, 2) the number of formed EBs after 3 days of cell plating, 3) EB’s size, and 4) the occurrence of the cells with different tissue specificity (in our case we assessed ESC differentiation into cardiomyocytes). It was demonstrated that the time of EBs formation was similar for all ESC cell lines (es-neok, es-pcDNA3, es-tat, and es-nef). No significant differences in EBs sizes in these lines were revealed either. However, the number of the EBs was different: it was approximately 2 times less in the es-tat cell line than in the es-pcDNA3 line, whereas, some increase (approx. 1.4 time) in the number of  EBs  was observed in the es-nef line as compared to the   es-neok cell line (Table 1). Again no differences in the quantity of EBs between two control cell lines were observed.
The areas of contracting cardiomyocytes started appearing on the 5-6th day after the EBs attachment to the carrier in the es-tat and es-nef ESC lines. The amount of EBs with the clusters of contracting cardiomyocytes was higher in es-nef cell line, and it was considerably lower in the es-tat cell line against control cells (Table 1).

The effects of the tat and nef on ESC differentiation into glial and neuronal cells
    The influence of the tat and nef genes of HIV-1 on the differentiation of mouse ESC into neuronal and glial cells in the presence and absence of retinoic acid was studied. Retinoic acid (RA) is well known inducer of neuronal differentiation (35, 36). To study neuronal and glial differentiation EBs were incubated in the presence or absence of retinoic acid as described in “Material and Methods” and transferred to 4 well plates coated with 0.01% gelatin. After 10 days part of the wells were stained with antibodies to GFAP, nestin or MAP2.
     No significant differences in the number of GFAP-positive cells were observed between all cell lines in the presence and absence of retinoic acid. Thus, both viral regulatory genes did not essentially affect the differentiation of ESC into glial cells.
     The number of nestin-positive cells was unchanged in the tat genetransfected cells, but it was decreased to none in nef-transfected cells (Table 2). Therefore, the nef gene apparently suppressed neuronal differentiation of ESC. However, in the presence of retinoic acid the number of nestin-positive cells was greater in es-nef as compared with es-tat and control cell lines (Table 2).
Terminally differentiated neuron cells were stained with antibodies against MAP2. In contrast to the tat gene transfected and control cells, the cultures of the nef gene transfected ESC in the absence of retinoic acid completely lacked MAP-positive cells. In the presence of retinoic acid, MAP2-positive cells could be observed in all cell lines, but the number of these cells being 2-2.5 fold higher in es-nef cell line as compared with es-tat cell line and control cells (Table 2).

	DISCUSSION

    An increase in proliferating activity was observed in the mouse ESC under the influence of the tat gene and its suppression under the influence of the nef gene. The result was consistent with our previous data obtained in different rat cell lines (Rat-2 line pseudonormal cells and pheochromocytome cells line PC-12) (17).

    Data obtained in this work is shown for the first time that both viral regulatory genes affect not only ESC proliferation, but have the profound effects both on early stages of ESC differentiation (EBs formation) and on the processes of their differentiation into cardiomyocytes and neuronal cell types.

    The effects of the tat and nef genes on ESC were apparent as early as at the stage of EB formation, and they were strictly opposite. Whereas tat hampered the EB formation, the nef gene significantly stimulated this process. The impact of these genes was detected also at later stages of ESC differentiation.

    HIV-1 cardiomyopathy has become one of the major causes of death in AIDS patients, but its pathogenesis is unclear. Here, we have for the first time shown that the expression of the tat gene reduced spontaneous differentiation of ESC into cardiomyocytes. The Tat protein of HIV-1 is a powerful activator of viral genes expression. Besides this essential function of the HIV-1 promoter, the Tat also exerts a remarkable number of other biological activities including the effects on cell proliferation, differentiation and cell death (37).  Moreover it has been shown that Tat can induce apoptosis in different cells, including cardiomyocytes (38). Our results showing the suppression of cardiomyocytes formation in tat-transfected cultures are in agreement with these data.

    From the other hand, it is well known that Tat protein has been suspected of causing neuronal disfunction that often leads to the development of HIV-associated dementia in AIDS patients. The treatment of neuronal cells with Tat affects the nerve growth factor (NGF) signaling pathway (39). However, we did not find any essential influence of tat on the processes of neuronal or glial differentiation in vitro, using the mouse ESC model.

    The effects of the nef gene on ESC are generally opposite to those of the tat gene. We have shown earlier that the nef gene decreased cell proliferation in different rat cell lines in vitro (16, 17). In the present work we have shown that proliferation of ESC was also decreased in the nef-transfected cell line. Moreover, our results allowed us to reveal a new potential of the nef gene. It was found to induce spontaneous differentiation of ESC cells into EB and cardiomyocytes, but at the same time to completely inhibit spontaneous neuronal differentiation. The latter is in agreement with earlier data that Nef can mediate neural cell death (12, 23, 40, 41). The nef gene does not express in neurons of HIV-infected patients, therefore, some observed pathological effects in nervous system may be due to its expression in glial cells.

    Unexpectedly, the nef gene does not suppress the retinoic acid induction of ESC differentiation into neurons, it can even slightly stimulate this process. It might be due to a possible anti-apoptotic effect of Nef (42) on neuronal cells partially neutralizing the pro-apoptotic effect of retinoic acid (43) when Nef cytotoxicity is attenuated by this acid.  Such a ‘neutralization’ might occur e.g. due to retinoic acid suppression of synthesis of interferon-inducible protein 10 (IP-10) (44) also involved in the Nef protein mediated neuronal cell death (12).

    In common, the reverse correlation between the effects of the tat and nef viral genes on ESC proliferation and differentiation were observed.  Genetic modifications of ESC is a perspective approach not only for the investigations of the role of different genes in the processes of cellular and tissue differentiation but for the creation of the models for drug testing and for development of the new approaches to human cell therapy in the  future.

	ACKNOWLEDGEMENTS

    The authors are grateful to Tishchenko N.A. for technical assistance, Dolotov O.B. for secretarial assistance, Varshaver N.B. for helpful discussion of the results and M. Lagarkova for kindly presenting of SSEA-1 antibodies.

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