INTRODUCTION

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Herpes simplex virus type 1 (HSV-1) is an important human pathogen which causes recurrent infections in epithelia between long periods of latency in neuronal cells (23, 58). The basis of the differences between lytic infection (which involves active and abundant transcription from the whole viral genome) and latency (a state of transcriptional quiescence of the bulk of the genome) has been the subject of intense research. There is now a wealth of information on the lytic transcriptional program of HSV-1 and the viral regulatory proteins which stimulate viral gene expression, but less is known about the difference in host cell functions which might contribute to the differing outcomes of infection in neuronal and non-neuronal cells.

One aspect of host cell biology which has become of interest in recent years and which could conceivably modulate HSV-1 infection is the function and status of small nuclear substructures known as ND10, PML nuclear bodies, or promyelocytic oncogenic domains (11, 37, 38, 53). At the early stages of infection, the parental genomes of HSV-1 and several other DNA viruses preferentially localize in the vicinity of ND10. It has been demonstrated that transcription of viral immediate-early (IE) genes occurs at these sites, from which viral replication centers later originate (26, 36). Many DNA viruses encode regulatory proteins that interact directly with ND10, first colocalizing with the cellular protein constituents and then disrupting these structures. This is especially well understood in the case of HSV-1 regulatory protein ICP0, which disrupts both ND10 and centromeres by inducing the proteasome-dependent degradation of several of their constituent proteins (12, 37, 38). HSV-1 mutants that do not express active ICP0 have a marked defect in the ability to initiate the lytic cycle after low-multiplicity infection and instead are likely to enter a quiescent state in which all viral transcription is silenced. A number of studies have demonstrated that the ability of ICP0 to affect ND10 and centromeres is concordant with its ability to stimulate virus infection, so it has been proposed that degradation of at least one of the known cellular targets of ICP0, or the mechanism by which this occurs, is an important factor in the balance between active and quiescent infection (12). This background led us to investigate the status of ND10 in neuron-like cells.

A number of previous studies have used neuronal cells of various origins. Rat and mouse neuroblastoma cell lines that can be differentiated into a neuron-like morphology have been found to be poorly infected by HSV-1 (56, 57). This defect has been attributed to poor IE gene transcription (29) and can be overcome in part by treatment with butyrate (1, 28) or release of the cells from growth arrest (47). It has been suggested that poor IE transcription in neuronal cells is caused by the repressive effects of Oct-2 transcription factors which bind to the TAATGARAT IE regulatory elements, thereby inhibiting Oct-1- and VP16-mediated transactivation (33, 34), but these studies have remained controversial (24). Whatever the mechanism of repression, the result is that it is possible to establish cultures of rodent neuron-like cells that harbor quiescent HSV-1 genomes for long periods (2, 56). Experiments with neurons explanted from rat embryonic dorsal root ganglia have extended these studies and demonstrated that in these true neuronal cells long-term quiescent infections can be established and used to investigate the processes controlling viral quiescence and reactivation (51, 59).

Rodent cells are not amenable to examination of their ND10 structures since most of the available antibodies recognize only the human forms of the major constituent proteins. Therefore, we sought to use a suitable human neuron-related cell line for our experiments. Human neuroblastoma cell lines have been used in a number of HSV-1 infection studies. Such cells are permissive for viral replication after high-multiplicity infection (4, 5), and the use of infection at supra-optimal temperatures has allowed the establishment of quiescently infected cultures which can later be reactivated (31). We chose to study the well-characterized neuronally committed teratocarcinoma NT2 cells which grow well in culture but can be differentiated into neuron-like hNT cells after treatment with retinoic acid (41, 42). NT2 cells are permissive for high-multiplicity HSV-1 infection (30), but low-multiplicity infections and the influence of ICP0 have not been analyzed in these cells. It had previously been noted that NT2 cells express low amounts of the major ND10 protein PML (32) and that Sp100 (another major ND10 constituent) appeared to be absent (27), but the fate of these proteins during differentiation and HSV-1 infection had not been studied.

The aims of this study were severalfold. We set out to investigate in detail the status of ND10 in both NT2 and hNT cells and to monitor the fate of ND10 and the major constituent proteins during HSV-1 infection. We also studied the ability of HSV-1 to infect both NT2 and hNT cells, and we assessed the role of ICP0 in these infections. Finally, we characterized the ability of ICP0 to affect ND10 proteins, to stimulate virus infection, and to activate gene expression in these cell lines. Our results demonstrate that ND10 are highly aberrant in NT2 cells but become more like those in other cultured cells after differentiation. HSV-1 replicated with reduced efficiency in both cell lines, especially in low-multiplicity infections, and this correlated with a reduced ability of ICP0 to disrupt ND10 and centromeres. Finally, we found that ICP0-deficient viruses can attain a quiescent state in infected NT2 and hNT cells and can be subsequently reactivated by superinfection with viruses which express ICP0. These results suggest that NT2 and hNT cells provide a promising system in which to study HSV-1 infection in neuron-related cultured cells of human origin.

	MATERIALS AND METHODS

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Cells and cell culture. The Ntera 2/D1 (NT2) cell line was obtained from Stratagene and was grown in Dulbecco's modified Eagle medium (DMEM) with nutrient mixture F12 (Gibco), supplemented with 4 mM glutamine, 10% fetal calf serum (FCS), and 100 U of penicillin and 100 µg of streptomycin per ml. Differentiation of NT2 cells into the neuronal phenotype hNT cells was done according to the supplier's protocol. Briefly, 10⁶ NT2 cells were seeded into 25-cm² flasks with 5 ml of medium containing 10 µM all-trans-retinoic acid (ATRA). The culture medium was changed three times per week for 6 weeks, and then the cells were transferred to a 75-cm² flask in medium without ATRA and cultured for an additional 2 days. The loosely adherent hNT cells were then recovered in the culture medium by striking the flask sharply, resulting in a population of cells with more than 30% having a significant neuronal morphology, and all the recovered hNT cells expressed high levels of Sp100 (see below).

Viruses. HSV-1 strain 17+ was the wild-type virus used in these experiments, from which the ICP0-null mutant virus dl1403 had been derived (54). Other viruses with lesions in ICP0 were the RING finger deletion mutant FXE (10) and virus M1, which has point mutations in the USP7 binding region (21). Virus tsK contains a temperature-sensitive mutation in ICP4, which results in failure to activate early and late gene expression and high level production of the other IE proteins at the nonpermissive temperature of 38.5°C (44). Virus in1330 carries a human cytomegalovirus (HCMV) lacZ cassette inserted into UL43, the ICP4 tsK mutation, and a deletion in the ICP0 coding region inducing a frameshift in codon 105 (25).

Antibodies. The following antibodies were used: anti-ICP0 monoclonal antibody (MAB) 11060 (16) and anti-ICP0 polyclonal rabbit serum r190 (19), anti-ICP4 MAB 10176 (15), anti-UL39 rabbit serum r76 (6), anti-UL42 MAB Z1F11 (50), anti-UL29 rabbit serum r515 (35), anti-PML rabbit serum r8 (3), and anti-PML MAB 5E10 (55), anti-Sp100 polyclonal rabbit serum SpGH (52), anti-hDaxx rabbit serum r1866 (43), anti-CENP-C rabbit serum r554 (48), and human anti-centromere autoimmune serum GS (ACA-GS) (7). Anti--galactosidase rabbit serum r12741/2 was a gift from Howard Marsden. Secondary antibodies for immunofluorescence were used at the indicated dilutions: fluorescein isothiocyanate-conjugated sheep anti-rabbit immunoglobulin G (IgG; 1/100; Sigma), Cy3-conjugated goat anti-mouse IgG (1/500) and goat anti-rabbit IgG (1/5,000), and Cy5-conjugated goat anti-rabbit IgG (1/500) (Amersham). Horseradish peroxidase-conjugated sheep anti-mouse and goat anti-rabbit secondary antibodies for use in Western blotting were obtained from Sigma.

Immunofluorescence. Cells were seeded onto coverslips in Linbro wells at a density of 10⁵ cells per well 1 day prior to infection or transfection. After appropriate infection or transfection, cells were fixed with formaldehyde (5% [vol/vol] in phosphate-buffered saline [PBS] containing 2% sucrose) and then permeabilized with 0.5% NP-40 in PBS with 10% sucrose. The primary antibodies were diluted in PBS containing 1% NBCS. Antibodies were used at the following dilutions: 11060, 1/1,000; r8, 1/1,000; r190, 1/200; r515, 1/200; SpGH, 1/1,000; r1866, 1/1,000; ACA-GS, 1/20,000; and r12741/2, 1/1,000. After incubation at room temperature for 1 h, the coverslips were washed at least six times and then treated with secondary antibodies. After a further 60-min incubation, the coverslips were again washed at least six times and mounted using Citifluor AF1.

Confocal microscopy. Samples were examined using 543-nm and 488-nm excitation lasers of a Zeiss LSM 510 confocal microscope (a Zeiss Axioplan with a ×63 oil immersion objective lens, NA 1.4). The data from the channels were collected sequentially using the appropriate band-pass filters built into the instrument. The scanning conditions were adjusted to ensure that signal overlap between channels was essentially eliminated. Data were collected with fourfold averaging at a resolution of 1,024 × 1,024 pixels using optical slices of between 0.5 and 1 µm. Data sets were processed using the LSM 510 software and then exported for preparation for printing using Photoshop.

Western blotting. Sodium dodecyl sulfate-polyacrylamide gels were prepared and run in the Bio-Rad MiniProtean II apparatus, and then the proteins were electrophoretically transferred to nitrocellulose membranes according to the manufacturer's recommendations. After a blocking step in PBS containing 0.1% Tween 20 (PBST) and 5% dried milk overnight at 4°C, the membranes were incubated with primary antibody in PBST-5% dried milk at room temperature for 4 h and then washed in PBST at least six times before incubation with horseradish peroxidase-conjugated secondary antibody in PBST-2% dried milk at room temperature for 1 h. After an extensive washing, the filters were soaked in Amersham or NEN Enhanced ECL reagent and exposed to film. Antibodies were stripped from the membranes following the Amersham ECL protocol, and the membranes were reprobed as necessary.

Plasmids, transfection of cultured cells, and CAT assays. The following plasmids were used for transfection assays: pCI110 (21), pSS80 (18), p175 (9), pCIPIC1 (20), and pgDCAT (8). Plasmid pCI-rtag-cICP0 contains the ICP0 cDNA coding region linked to an N-terminal oligonucleotide encoding an epitope from the C terminus of UL30, inserted into the expression vector pCIneo (Promega). Plasmids were transfected into Vero and NT2 cells using Lipofectamine Plus reagent (Gibco-BRL) using 0.5 µg of total DNA and 1 µl of reagent per 10⁵ cells. For chloramphenicol acetyltransferase (CAT) assay transfections, 10 ng of pSS80 reporter was used, and plasmid pUC9 was used to equalize the total amounts of DNA; the amount of the ICP0 expression plasmid varied between 5 and 500 ng (see Fig. 7). Transfected cells were fixed and stained for immunofluorescence, harvested for Western blotting, or used to prepare CAT assay extracts about 24 h later. The ability of ICP0 to activate gene expression in transfected cells was determined using reporter plasmids pSS80 and pgDCAT, which contain the CAT gene linked to the HSV-1 ICP6 and glycoprotein gD gene promoter regions, respectively. Cells in Linbro wells were transfected as described above, and then whole sonicated cell extracts were prepared and used for estimation of CAT activity using radiolabeled chloramphenicol as substrate, essentially as described elsewhere (8). Initial experiments determined the optimal amounts of reporter and activator plasmids to be used in each cell type. The transfection experiments were repeated on several independent occasions in parallel with positive and negative controls.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Neuronal committed teratocarcinoma NT2 cells have highly abnormal ND10. The first stage of this project was to compare the composition and morphology of ND10 in neuronal committed NT2 and fibroblast HFL cells. Double staining for the major ND10 antigens PML and Sp100 showed the normal extensive colocalization of the two proteins in multiple punctate nuclear foci in HFL cells, but the overwhelming majority of NT2 cells had only background levels of Sp100 (27) and fewer PML foci (Fig. 1A). The distribution of PML was unusual in many NT2 cells, commonly with strings, tracks or lines of small foci extending through the nucleoplasm. One of the NT2 cells shown in Fig. 1 has two moderate examples of this phenotype, but many others had PML tracks similar to those in the hNT cells shown in Fig. 1A. In HFL cells, the PML-associated protein hDaxx (27) was present throughout the nucleus and in local accumulations which in many cases strongly colocalized with PML (Fig. 1A). In contrast, in NT2 cells hDaxx was much less well associated with PML (Fig. 1A) and the distinct accumulations of hDaxx were instead preferentially associated with centromeres (Fig. 1B). This is reminiscent of recent data which showed that hDaxx can be present at both ND10 and centromeres, and its relative association with these structures can be influenced by cell status (22). In contrast to the abnormal ND10, the staining pattern of centromere protein CENP-C in NT2 cells was similar to that in HFL cells (Fig. 1A).

View larger version (33K): [in this window] [in a new window]   FIG. 1.   Distinct expression patterns of ND10 and centromere proteins in HFL, NT2, and hNT cells. Confocal micrographs of the three cell lines are presented, as indicated by white lettering. (A) The labeled proteins are indicated in the top row and are the same in each vertical row of panels. PML was stained with mouse MAb 5E10 (green), and the cells were also costained with SpGH (lefthand panels), rabbit serum r1866 (center panels), or rabbit serum r554 (righthand panels) for Sp100, hDaxx, and CENP-C, respectively. There is no Sp100 expression and less PML expression in NT2 cells, and PML does not colocalize efficiently with hDaxx. In HFL and hNT cells, PML extensively colocalizes (yellow) with Sp100 and hDaxx but not with CENP-C. (B) Localization of hDaxx (green) and centromere proteins (red). Cells were double labeled with r1866 and human serum ACA-GS which contains antibodies against several centromere proteins. In NT2 cells, a significant proportion of centromeres are associated with local accumulations of hDaxx, but this occurs more rarely in HFL and hNT cells.

View larger version (56K): [in this window] [in a new window]   FIG. 2.   Western blot analysis of the expression patterns of Sp100 and PML in HFL, NT2, and hNT cells. The lefthand three tracks show PML species detected by 5E10, with actin detected simultaneously as the internal control. The righthand three lanes show the same filter after stripping and reprobing for Sp100 with SpGH. The arrowheads mark the presumed SUMO-1-modified forms of PML and Sp100. NT2 cells do not express Sp100, whereas in hNT cells long-term induction of retinoic acid results in a drastic increase of both unmodified and modified forms of Sp100 and PML. The extent of SUMO-1 modification of PML is reduced in NT2 cells.

Differentiation of NT2 cells into neuron-like hNT cells restores ND10 structure. NT2 cells can be induced to differentiate into nondividing hNT cells by treatment with retinoic acid for several weeks (41). The resultant hNT cells acquire a neuron-like morphology and express a number of neuron-specific markers (42). Staining of hNT cells for PML and Sp100 revealed that, in great contrast to the parental NT2 cells, hNT cells have striking ND10 with prominent foci of both proteins colocalizing precisely (Fig. 1A). Again, tracks or chains of small beads of PML were common. A further difference between NT2 and hNT cells was that in the latter hDaxx was strongly associated with PML (Fig. 1A) and much less well associated with centromeres (Fig. 1B). These data correlate with strikingly increased amounts of both Sp100 and PML, and particularly SUMO-1-modified PML, in hNT cells (Fig. 2). Since hDaxx does not interact with Sp100 (27), this result strengthens the conclusion that the distribution of hDaxx is dependent on PML and its modification. Thus, either ATRA itself or the process of differentiation induces substantial changes in the quantities of PML and Sp100 present in the cells, with consequent alterations in ND10 appearance and composition. Our previous examination of the precursor NT2 cells had found occasional cells with prominent ND10 containing both PML and Sp100 (data not shown), and it is likely that these cells represent the small number of cells which are known to undergo spontaneous differentiation in NT2 cultures. Time course experiments showed that the increased amounts of Sp100 appeared after at least 3 weeks of treatment with retinoic acid, which implies that these changes result from the process of differentiation rather than from a simple induction of PML and Sp100 transcription by retinoic acid.

HSV-1 replicates poorly in NT2 and hNT cells. As detailed in the introduction, previous work found that HSV-1 has a growth defect, particularly in low-multiplicity infections, in rodent neuroblastoma cell lines or cells which could be differentiated into a neuron-like state. Equivalent studies on HSV-1 infection of human neuroblastoma cell lines had not investigated low-multiplicity infections in any detail, and there was no information on the requirement for and functionality of ICP0 in such cells. Therefore, we compared the efficiency of HSV-1 replication in HFL and NT2 cells. An initial time course experiment using a multiplicity of 1 PFU per cell showed that the virus replicated slightly more slowly in NT2 cells than in HFL cells, but by 36 h the yield of virus was only moderately reduced. Extending the incubation period to 48 h did not significantly alter the results from those obtained at 36 h (Fig. 3). A series of parallel infections were conducted on NT2 and HFL cells at multiplicities varying from 50 to 0.01 PFU per cell, and the progeny virus was harvested and titrated 36 h later. This length of incubation allows multiple rounds of viral replication in HFL cells, so the final yields were not significantly affected by input multiplicity in this cell type (Table 1). In contrast, at an input multiplicity of 0.01, the yield of virus was reduced 400-fold in NT2 compared to HFL cells (Table 1). Similar results were obtained after extending the incubation period to 48 h, which indicates that the defect cannot be explained simply by delayed kinetics (Table 2). Comparison of NT2 and hNT cells in parallel experiments demonstrated that HSV-1 17+ replicated slightly less well in the differentiated cells at all multiplicities, but the differences between NT2 and hNT cells were small compared to those between NT2 and HFL cells (Table 1). We attempted to compare the plating efficiency of the virus in the three cell lines but, because of the poor growth in NT2 and hNT cells, plaque formation on these cells was too poor to be scored.

View larger version (16K): [in this window] [in a new window]   FIG. 3.   Growth curves of HSV-1 strain 17+ in HFL and NT2 cells. Cells were infected with the virus at 1 PFU per cell, and both cells and medium were harvested at the indicated times after infection; progeny virus titers were then determined on BHK cells. The data are the average of two independent experiments.

ICP0-deficient mutants also replicate poorly in NT2 and hNT cells. Next, we compared the growth efficiencies in HFL and NT2 cells of ICP0-null mutant virus dl1403 and the USP7-binding negative mutant M1. Deletion dl1403 has been characterized as having a severe multiplicity-dependent growth defect in HFL cells (54), while the interaction with the ubiquitin-specific protease USP7 was found to contribute to ICP0 function in BHK cells and to a lesser extent in HFL cells (13, 21). To compare the yields of these viruses in the various cell types, we first determined the titers of the viral stocks on U2OS cells in which ICP0 function is not required, thus allowing efficient replication of wild-type and all ICP0 mutant viruses (60). We then infected HFL and NT2 cells with each virus at multiplicities based on the titers in U2OS cells and titrated the progeny virus in U2OS cells. Increased input multiplicities of dl1403 were used in order to initiate a productive infection. As expected, at 36 h after infection, dl1403 replicated poorly in HFL cells compared to the wild-type virus; even with the input virus increased 500-fold, yields were reduced by an order of magnitude (Table 2). At the highest multiplicity used, the yield of dl1403 was reduced by a further order of magnitude in NT2 cells compared to HFL cells, and extending the incubation period to 48 h did not significantly affect the results (Table 2). Virus M1 also replicated much less efficiently in NT2 compared to HFL cells at all multiplicities tested (Table 2), indicating that the ability of ICP0 to bind to USP7 is apparently very important for virus replication in NT2 cells. These data provide the most striking indication obtained so far that the ICP0-USP7 interaction is important for HSV-1 replication in certain situations. As with wild-type virus (Table 1), the replication efficiencies of the two mutant viruses in hNT cells were similar to those in NT2 cells, with dl1403 replicating slightly less well and M1 replicating slightly better in the differentiated cells (Table 2).

Viral gene expression is abnormal in NT2 and hNT cells. To investigate the basis of the poor growth of HSV-1 in NT2 and hNT cells, we compared viral gene expression in the two cell types with that in the fully permissive HFL cells. Whole-cell extracts were prepared at various times after infection and probed with a mixture of antibodies recognizing representative IE and early gene products; we probed for ICP0, ICP4, the large subunit of ribonucleotide reductase UL39 (ICP6), the major DNA-binding protein UL29 (ICP8), and the DNA polymerase accessory factor UL42. It should be noted that, because of the varied antibody sensitivities, this Western blot approach compares the relative expression of this group of proteins in the different samples rather than measuring absolute protein levels. At a multiplicity of infection of 5 there was, as might be expected on the basis of the titration data, little difference in the patterns and time course of viral gene expression in HFL and NT2 cells (Fig. 4A). However, reduction of the multiplicity to 1 PFU per cell revealed an intriguing phenotype. At 2 h postinfection, some UL29 expression was detectable in HFL cells, but viral gene expression in NT2 cells was restricted to ICP0 (Fig. 4B). At 3 h UL29 and UL39 expression was well marked in HFL cells but, compared to the expression of ICP0, was much reduced in NT2 cells. By 4 h the early viral gene products accumulated in NT2 cells, but their expression levels compared to ICP0 were still reduced from those seen in HFL cells. These effects were more pronounced at a multiplicity of infection of 0.2 (Fig. 4C). In hNT cells, even at 4 h after infection with a multiplicity of 5, the expression of UL29 and UL39 was only just detectable (Fig. 4A). Since ICP0 is expressed with greater or equivalent efficiency in NT2 and hNT compared to HFL cells, these data suggest that the virus is entering NT2 and hNT cells but that the infection progresses from the IE to later stages inefficiently.

View larger version (63K): [in this window] [in a new window]   FIG. 4.   Comparison of the rates of viral gene expression in HFL, NT2, and differentiated hNT cells. Cells were infected with 5 (A), 1 (B), or 0.2 (C) PFU of wild-type HSV-1 strain 17+ per cell and harvested before infection (lanes m) and at 1, 2, 3, and 4 h after absorption (hpa) and then processed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blot analysis. A mixture of antibodies recognizing several viral proteins was employed to detect IE proteins ICP0 and ICP4 and also the early genes UL39, UL29, and UL42 (as indicated on the left).

View larger version (74K): [in this window] [in a new window]   FIG. 5.   Inefficient progression of viral infection in NT2 and hNT cells. HFL (top panels), NT2 (middle panels), and hNT (bottom panels) cells were infected with wild-type HSV stain 17+ at 1 PFU per cell. Infected cells were fixed 8 h after absorption and prepared for immunofluorescence and simultaneous staining for ICP0 (lefthand panels) and UL29 (righthand panels), using MAb 11060 and serum r515 as markers of viral IE and E gene expression. In hNT cells, the number of infected cells expressing ICP0 and UL29 is much less than in HFL and NT2 cells. The number of NT2 cells expressing ICP0 is equivalent to the HFL infections, but relatively few NT2 cells are expressing large amounts of UL29.

ICP0 affects ND10 and centromeres more slowly in NT2 cells than in HFL cells. ICP0 causes major effects on the cell by inducing the degradation of PML, Sp100, and CENP-C, thereby disrupting both ND10 and centromeres (12). We therefore compared the efficiency by which ICP0 induced these effects in HFL, NT2, and hNT cells. Cells were infected with HSV-1 17+ at a multiplicity of 1 and then stained for ICP0 and the cellular proteins PML, CENP-C, and hDaxx at various times postinfection. In the early stages of infection, ICP0 colocalized with PML in all cell types, but as time progressed the rate at which the PML foci were disrupted in NT2 and hNT cells was noticeably slower than in HFL cells (Fig. 6 and Table 3). In this experiment, only 4% of infected HFL cells retained PML foci by 2 h postinfection, whereas 56% of NT2 cells did so. Even by 4 h postinfection, 54% of infected NT2 cells retained punctate PML staining (Table 3). Similar results were obtained in infected cells stained for CENP-C (Fig. 6 and Table 3) and hDaxx (Table 3). Loss of CENP-C from centromeres in infected HFL cells was extremely rapid, but in NT2 cells ICP0 markedly colocalized with CENP-C at early times of infection to a greater degree than in any other cell type we have studied (Fig. 6). It is intriguing that ICP0 associates so well with centromeres in this cell type, in which PML is poorly expressed and less well modified by SUMO-1 (Fig. 2) and in which hDaxx becomes more highly associated with centromeres than with ND10 (Fig. 1B). This suggests that ICP0 associates with a factor which can be present in both structures but is predominantly associated with centromeres in NT2 cells. At later times of infection, although about two-thirds of infected NT2 cells had lost CENP-C from centromeres (Table 3), in the remaining one-third ICP0 either remained at centromeres and CENP-C was much less completely degraded or ICP0 became more diffuse yet CENP-C remained in characteristic centromeric foci (Fig. 6). The results in hNT cells were similar to those in NT2 cells, except that with the increased expression of PML and its modification by SUMO-1 in hNT cells (Fig. 2), ICP0 strongly colocalized with PML yet inefficiently disrupted ND10 (Fig. 6). Correspondingly, ICP0 colocalized with centromeres less efficiently in hNT cells and again caused their disruption inefficiently (Fig. 6).

View larger version (38K): [in this window] [in a new window]   FIG. 6.   Comparison of the stability of ND10 and centromeres in HFL, NT2, and hNT cells at 2 and 4 h after the start of infection. HFL (top panels), NT2 (middle panels), and hNT (bottom panels) cells were infected with wild-type HSV stain 17+ at 1 PFU per cell. After various times of infection, cells were fixed and stained for ICP0 (MAb 11060) and PML (r8) (lefthand pairs of panels) or ICP0 and CENP-C (r554) (righthand pairs of panels). Both ND10 and centromeres, as judged by PML and CENP-C staining, are more stable in infected NT2 and hNT than in HFL cells.

Evidence that ICP0 activates gene expression poorly in NT2 cells. To obtain more direct evidence that ICP0 activates gene expression less efficiently in NT2 cells, we assessed the activation of gene expression induced by HSV-1 IE proteins in transfected cells. Because HFL cells transfect very poorly, we compared the results using Vero and NT2 cells. Initially, we optimized the amount of pSS80 (a reporter plasmid containing the ICP6 promoter linked to the CAT gene) required to give low levels of basal activity, and then we cotransfected the cells with increasing amounts of the ICP0 expression vector pCI-rtag-cICP0. In Vero cells, maximal activation was obtained using 5 to 50 ng of pCI-rtag-cICP0, while higher amounts had less effect (Fig. 7). However, in NT2 cells pCI-rtag-ICP0 did not give any significant activation of gene expression (Fig. 7). Although Western blotting of the extracts showed that ICP0 was slightly less well expressed in NT2 cells, 20 ng of pCI-rtag-ICP0 in NT2 cells gave greater expression of ICP0 than 5 ng in Vero cells, yet it failed to activate gene expression (Fig. 7).

View larger version (42K): [in this window] [in a new window]   FIG. 7.   Comparison of the transactivation of an ICP6 expression cassette by ICP0 in NT2 and HFL cells. Cells were cotransfected with reporter plasmid pSS80 (ICP6 promoter linked to the CAT gene) and the indicated amounts of the ICP0 expression plasmid pCI-rtag-cICP0 (see Materials and Methods). The Western blot analysis of the total cell proteins of samples transfected in parallel with the same amount of plasmid and probed for ICP0 is shown below. The results of this single experiment were reproduced on several independent occasions, and similar results were obtained with a reporter containing the glycoprotein gD promoter.

Low-multiplicity infection of NT2 and hNT cells produces quiescently infected cells which can be reactivated by ICP0 expressed by a superinfecting virus. Previous studies have shown that infection by ICP0 mutant viruses can result in the maintenance of quiescent genomes in nonproductively infected cells and that these genomes can be reactivated by later expression of exogenous ICP0 (46). The poor infection of NT2 cells by both wild-type and ICP0 mutant viruses and the apparently poor function of ICP0 in NT2 cells suggests that a similar situation could be occurring in these cells. Recent studies of this type have used heavily defective viruses to reduce the initial viral infectivity as much as possible, but the very poor growth of dl1403 on NT2 cells allowed the examination of quiescent infection with dl1403/lacZ, a relatively viable virus which carries a lacZ gene driven by the HCMV promoter and the dl1403 ICP0 deletion.

View larger version (79K): [in this window] [in a new window]   FIG. 8.   Establishment of quiescently infected NT2 and hNT cells using an ICP0-deficient virus and reactivation by superinfecting ICP0-positive virus. Cells were infected as described in Materials and Methods. NT2 (upper field) and hNT (lower field) cells were initially infected with dl1403/lacZ virus and then superinfected with HSV-1 strain 17+ (A), tsK (B), FXE (C), in1330 (D), 17+ in the presence of MG132 (E), or else were mock infected (F). NT2 and hNT cells were fixed 8 and 16 h postsuperinfection, respectively, and then stained for -galactosidase expression by immunofluorescence. Quiescent virus can be reactivated by viruses expressing functional ICP0 viruses (A and B) but not by ICP0-deficient viruses (C and D) or if the ICP0 activity is inhibited by MG132 (E).

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

In this study we have compared the expression and distribution of selected ND10 proteins in human fibroblast HFL, neuronal precursor NT2, and differentiated neuron-like hNT cells and then compared their infection by HSV-1 and the functionality of ICP0 in the three situations. We found striking differences in ND10 structure between HFL and NT2 cells and further substantial changes in the differentiated hNT cells. Both NT2 and hNT cells were poor hosts for HSV-1 replication, particularly in low-multiplicity infections, and the data suggest that a contributing factor to this poor growth could be the apparently poor functionality of ICP0 in both cell types.

Our results demonstrating negligible expression of Sp100 and low-level expression of PML in NT2 cells correlate well with previous studies (27, 32), but we have extended the previous data by demonstrating highly aberrant PML track structures in many NT2 and hNT cells and a relatively low proportion of SUMO-1-modified PML in NT2 compared to HFL cells. Differentiation of NT2 into nondividing hNT cells resulted in massive increases in the expression of both PML and Sp100, which correlated with the establishment of prominent ND10 foci in which the two proteins strongly colocalized. Since this effect occurred only after several weeks of ATRA treatment, it is likely that it is in some way associated with the process of differentiation rather than with the ATRA treatment itself. This notion is consistent with the presence of low numbers of cells in NT2 populations which express high levels of Sp100, which are probably in the process of spontaneously differentiating.

Previous studies using cultured cells with neuronal features for HSV-1 infection have concentrated on rodent cell lines such as mouse C1300 neuroblastoma cells and derivatives (28, 29) or cells derived from rat PC12 cells (47, 56). Similar to our present results, these rodent cell lines were found to be poor hosts for HSV-1 infection in low-multiplicity infections. The advantage of the human NT2 and hNT cells is that it is possible to correlate the efficiency of viral infection with the effects of ICP0 on ND10 and centromeres since most available antibodies against components of these structures recognize the human but not the equivalent rodent proteins. We found that despite early expression of ICP0 in NT2 and hNT cells, the progression of viral gene expression into the pattern characteristic of lytic infection was delayed. This correlated with relatively slow disruption of ND10, prolonged and striking association of ICP0 with centromeres (in NT2 cells), and inefficient induced loss of centromere protein CENP-C. It is unlikely that these effects are a nonspecific consequence of the generally poor infection because ICP0 can disrupt ND10 and centromeres in the absence of other viral proteins. Indeed, the observations that ICP0 is relatively abundantly expressed in NT2 cells, as detected by Western blotting, and the slow disruption of ND10 and centromeres in cells that are clearly expressing ICP0 suggests that ICP0 function itself may be compromised in these cells. This contention is supported by the transfection experiments which suggest that ICP0 is a poor activator of gene expression in NT2 cells.

Our results are also relevant to the debate on whether the degradation of ND10 proteins PML and Sp100 specifically contributes to ICP0 function or whether it is the process by which this degradation occurs which is important. Although NT2 cells express relatively low levels of PML and no detectable Sp100, while hNT cells express hugely increased amounts of both proteins, hNT cells are only slightly less permissive for HSV-1 infection than are NT2 cells. While many other factors may be affecting the efficiency of viral replication in these two cell types, it is clear that the endogenous expression levels of PML and Sp100 are not dominant factors.

The replication efficiency of ICP0-deficient viruses is known to be very dependent on cell type, such that the probability of an ICP0 mutant establishing a lytic infection in HFL cells is reduced about 2,000-fold in HFL cells compared to U2OS cells (13, 60). NT2 and hNT cells are even more resistant than HFL cells to productive infection by dl1403 (Table 2). It is noteworthy that the poor growth of dl1403 in NT2 and hNT cells is not a trivial consequence of failure of the virus to enter the cells since, in a manner analogous to the establishment of quiescent infection in cultured cells using multiply defective viral genomes (45, 50), at least a proportion of the input dl1403 genomes can be reactivated by superinfection with viruses expressing ICP0. A potential application of these findings could be to investigate the control of gene expression from quiescent viral genomes in cultured human cells with neuronal characteristics.

We have shown that cultured human cells with neuronal characteristics are poor hosts for productive HSV-1 infection in a way that correlates at least in part with poor ICP0 functionality. Cells infected at a low multiplicity progress inefficiently into the lytic cycle, and in the absence of ICP0 many cells become quiescently infected. It is an interesting speculation that, if these observations hold true in human neuronal cells in vivo, a controlling factor in the establishment of latent infections in neurons in natural infections could be the relative activity of ICP0 in these cells.