Viruses have evolved complex molecular mechanisms to interact with their host genomes and utilize cellular machinery to ensure their reproduction and survival. These molecular mechanisms, which are useful targets for anti-viral drugs, have traditionally been studied in two-dimensional (2-D) cell cultures. However, many groups are reconsidering use of 2-D culture environments (i.e., tissue culture flasks, Petri dishes, and well plates) as increasing evidence suggests that cellular properties such as cytoskeletal arrangement, signal transduction, and cell differentiation, differ when cells are grown as 2-D monolayers compared to in a three-dimensional (3-D) environment.12.–3 These findings make intuitive sense, because a 3-D environment, including an extracellular matrix, more closely mimics a cell’s natural chemical and mechanical tissue microenvironment in the body.4,5
Differences in host-virus interaction dependent on culture environment have been previously reported,6,7 including culture-dependent hepatitis C virus (HCV) host-virus biology.8,9 HCV is a leading cause of chronic hepatitis worldwide, but patient-derived HCV strains cannot be effectively propagated in traditional monolayer cultures.10 So HCV infection could be studied in vitro, a recombinant HCV strain was developed that propagates in immortalized hepatocytes grown as monolayers.11 This recombinant culture system is limited in its relevance, however, motivating investigations utilizing different culture conditions, including hepatocytes cultured in a 3-D gel matrix that have been shown to better support the replication of clinical HCV isolates.12,13 This example illustrates that in order to better characterize host-virus interactions and improve virus culture, it may be worth the added complexity of 3-D culture systems to maintain a more physiologically relevant microenvironment.10 This shift to 3-D cultures introduces the challenge of imaging deeper in a more highly scattering environment.
In this study, we have used two-photon (2P) microscopy utilizing ultrashort, sub-10-fs pulses, which we call ultrashort pulse microscopy (UPM), to investigate differences in host-virus biology due to culture environment using cytomegalovirus (CMV) as a model for infection. Human cytomegalovirus (HCMV) is a ubiquitous virus that poses a serious problem for immune-compromised patients and neonates with immature immune systems, resulting in congenital malformations.14,15 mCMV, a murine homolog of HCMV, is an established model to study various aspects of CMV pathology both in animals (in vivo) and in culture (in vitro). Immortalized NIH 3T3 mouse fibroblasts are permissive to mCMV infection, and we selected this model since its cellular pathology is robust and well characterized. Sub-10-fs pulses utilized in UPM have very high peak powers (MJ), however, the overall average power deposited in cells is lower than in conventional 2P systems. The broadband spectrum of sub-10-fs pulses also leads to a large 2P power spectrum that efficiently excites fluorescence from a broad range of intrinsic and extrinsic fluorophores simultaneously.16,17 Consequently, UPM generates high 2P signals while preserving sample integrity and is thus ideal for time-lapse imaging.
Materials and Methods
Generation of NIH-3T3/H2B-GFP Cell Line and FACS Analysis
NIH-3T3 cells were transfected with 2 mg of H2B-GFP expression vector18 using LipofectAMINE according to manufacturer’s protocol (Gibco BRL, San Francisco, CA). Two days after transfection, medium was changed and 10 mg/ml blasticidine-S (EMD Millipore, Billerica, MA) was added. Five days later, the medium was changed to 2 mg/ml blasticidine-S. After 15 days of drug selection, cells were collected and cloned by limiting dilution with selection. Several clones were expanded and cultured for three months in the absence of blasticidine-S. Five of these clones continued strong GFP-H2B expression, which suggests that chromosome stability is unimpaired by constitutive H2B-GFP expression, and were selected for fluorescence activated cell sorting (FACS) analysis.
For FACS analysis, NIH-3T3 cells expressing the H2B-GFP construct were harvested by trypsinization and fixed in 70% ethanol for more than 3 h at 4ºC. Cells were stained with PI (20 mg/ml) containing RNAse (200 ng/ml). Fluorescence was measured using a FACScan (Becton Dickinson, Mountain view, CA). The red (PI) and green (GFP) emissions from each cell were used to measure DNA content and GFP-H2B fluorescence, respectively. Cell debris and fixation artifacts were gated out using Cell Quest software (Becton Dickinson). The brightest clone with normal cell cycle distribution, clone #2, was selected for further use.
Cell and Virus Cultures
NIH-3T3/H2B-GFP cells were maintained at 37°C in a 5% atmosphere in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% calf serum (CS), 2 mM L-glutamine, 100 U/ml penicillin and 100 mg/ml streptomycin. The Smith strain of mCMV (a gift from Dr. Ann Campbell, Eastern Virginia Medical School) was used, and stocks prepared in NIH-3T3 cells. Viral titers were determined by standard plaque assays.
For analyzing viral replication compartment (VRC) formation, NIH-3T3/H2B-GFP cells grown in 12-well dishes at 70% confluence were infected with mCMV at a multiplicity of infection (MOI) of 10 plaque forming units per cell (PFU/cell) with inoculum prepared with DMEM and 2% CS. After 1 h adsorption period at 37°C, the inoculum was removed, the cell cultures were washed once with phosphate-buffered saline (PBS), and fresh DMEM with 10% CS was added. For 3-D cultures, collagen gels were assembled with rat-tail type I collagen (Becton Dickinson), 5X DMEM, and reconstitution buffer, and neutralized with 1 M NaOH. NIH-3T3 cells were seeded in gels at 70% density (v/v) and were subsequently allowed to polymerize and equilibrate at 37°C and 5% in 12-well plates. Gels were infected with mCMV approximately one day later, also at a MOI of 10 under the same conditions as cells grown as monolayers in 12-well dishes.
Ultrashort Pulse Microscopy
The custom-built laser-scanning two-photon microscope used for ultrashort pulse microscopy (UPM) has been previously described.19 Briefly, sub-10-fs pulses from a passively mode-locked Ti:Sapphire oscillator with 800 nm center wavelength and 133 nm full-width half maximum (Femtolasers, Vienna, Austria) were pre-compensated (GSM 270, Femtolasers) and coupled by a galvanometer driven X–Y scanner (Cambridge Technology, Cambridge MA) into an upright microscope (Axioskop2 MAT, Carl Ziess). The beam was directed by a 635 nm short pass dichroic mirror (Chroma, Bellows Falls, VT) through the imaging objective to the sample. The two-photon excited GFP signal was then collected through the imaging objective (63X, 1.2 NA and 40X, 0.8 NA from Carl Zeiss) and separated using a 430 nm long-pass dichroic mirror (Chroma), further discriminated with a 525/50 nm bandpass filter (Chroma), and detected with a PMT (Hammamatsu. Bridgewater, NJ). Data acquisition was controlled with custom LabVIEW software (National Instruments, Austin, TX).
For time-lapse imaging, cell cultures were imaged in custom-built environmental chamber and maintained at 35°C with 5% with 3-5 mW power at the sample. Z-stacks were acquired every fifteen minutes at 0.5 μm steps over the course of imaging.
Z-stacks were converted to raw intensity images of chromatin structure (from GFP-H2B) with custom Matlab software (Mathworks, Natick, MA) and subsequent processing and quantification were performed with custom semi-automated Matlab routines. Three-dimensional reconstructions and VRC tracking were performed with ImageJ open source software.
To quantify chromosomal volume, we segmented the GFP-H2B signal. Each optical section from a z-stack was converted to binary mask with an automated algorithm based on Otsu’s method that minimizes intraclass variance between background (noise) and foreground (GFP-H2B) pixels. The sum of all binary masks in a z-stack was then converted from total number of voxels to spatial volume using the measured dimensions of each voxel for 63X and 40X objectives.
To quantify nuclear volume, we outlined the GFP-H2B signal and filled in that region to generate a mask of total nuclear area for each optical section. A binary mask was generated from each optical section of a z-stack with a 50% lower threshold than above, which better preserved the outline of the nucleus from the chromatin structure. To join edges that remained discontinuous in the outline of the nucleus, the binary mask was dilated using a 5 pixel structural disc-shaped element. The mask was then eroded using the same structural element to recover the original boundary with continuous edges and remaining negative spaces within the nucleus converted to 1’s. As with chromosomal volume, the sum of all binary masks in a z-stack was then converted from total number of voxels to spatial volume using the measured dimensions of each voxel for 63X and 40X objectives.
By transfection of NIH-3T3 cells with the H2B-GFP mammalian expression vector18 and selection with blasticidin, we obtained a polyclonal cell population that stably expressed an H2B-GFP transgene for tracking chromatin dynamics. Isolated clones were selected by FACS and by comparison of cell cycle distribution to those of the parental line [Fig. 1(a)]. Using UPM, we imaged these NIH 3T3/H2B-GFP cells infected with mCMV either as adherent monolayers in tissue culture plates or in collagen gels. In both 2-D and 3-D environments, cells were cultured in DMEM with 10% CS and inoculated in DMEM with 2% CS with the same number of plaque forming units (PFU) of virus per cell so that MOI was kept constant at . The collagen gel () used to construct the 3-D culture was seeded so that the cell density at the time of inoculation was 70% (volume), and in 2-D, cells were inoculated at 70% confluence (area). 2P signal generated from the GFP-H2B fusion was used to quantify nuclear parameters, similar to what has been previously reported [Fig. 1(c)].20 Briefly, semiautomated algorithms in Matlab were used to threshold the GFP signal to binary masks that were summed to find a cell’s chromatin volume. Then morphological operations (fill, dilate, and erode) were used on each 2-D mask to generate a smooth mask of the nucleus that was summed in 3-D for calculating total nuclear volume. The difference between the total nuclear volume and chromosomal volume is what we refer to as the interchromosomal volume. The z-axis was oversampled () so no chromosome details would be lost. 3-D reconstructions and VRC tracking were performed with ImageJ.
First, we imaged the cultures at 8 hours post infection (hpi), when the virus is known to be actively replicating.21 We found that at 8 hpi, the nuclear volume increases significantly due to expansion of VRCs (measured indirectly by expansion of interchromosomal space) in both 2-D and 3-D culture environments compared to mock infected controls. Interestingly, however, the increase in nuclear volume for infected NIH 3T3s cultured in collagen gels was significantly larger than the increase for infected NIH 3T3s cultured on well plates [Fig. 1(b)]. No compression of the host chromatin was measured at this point in the infection. Importantly, these data indicate that the extracellular matrix does not impede efficient infection of NIH 3T3s by mCMV and subsequent viral replication. In fact, the 3-D collagen culture environment enhances these processes either directly or indirectly.
We also characterized the dynamics of VRC formation from 8 to 16 hpi using UPM. Mock-infected cells maintain constant nuclear and chromatin volume between 8 and 16 hpi [Fig. 2(a) and 2(b)]. In both 2-D and 3-D culture environments, the nature of mCMV infection changed during the course of imaging, shifting from an expansion of nuclear volume with unchanged chromatin volume from 8 to 12 hpi to a dramatic decrease in both nuclear and chromatin volume from 12 to 16 hpi [Fig. 2(a) and 2(b)], indicating a compression phase. These findings are similar to those previously reported for the related alpha-herpes virus HSV-1.20 We observed a trend of somewhat slower rate of decrease in nuclear and chromatin volume in 3-D culture compared to 2-D culture, but this was statistically insignificant. We also observed a characteristic cytopathic effect of lytic infection begin to appear in both 2-D and 3-D cultures at approximately 16 hpi [arrows, Fig 2(a) and 2(b)]. This pathological feature, marked by the buckling of the nucleus, is more dramatic in the 3-D culture environment. Also of note, chromatin structure of the controls was remarkably stable over time, highlighting the usefulness of UPM for extended periods of live-cell imaging in both 2-D and 3-D culture environments.
Finally, utilizing the sub-cellular resolution of UPM, we tracked the dynamics of individual replication compartments within NIH 3T3 cells infected with mCMV in 3-D collagen cultures from 8 to 24 hpi [Fig. 3(a) and Video 1]. Our goal was to see if individual VRCs coalesce to form larger VRCs, as has been previously reported for the related alpha-herpes virus HSV-1.22 In this study, two easily distinguishable VRCs were identified at 8 hpi, marked by arrows [Fig 3(bI)). Sections from the lines on the image illustrate the separation of these VRCs by host chromatin and that they are indeed distinct from each other. Another separate VRC was identified at 9 hpi and marked also with an arrow [Fig. 3(bII)]. The two VRCs with arrows marked with an asterisk coalesce at 20 hpi [Fig. 3(bIII), but by 24 hpi, the two originally identified VRCs remain distinct. These data demonstrate similarities in the mechanisms of replication compartment formation and marginalization of host chromatin between alpha-herpesvirus HSV-1 and beta-herpesvirus mCMV.
Using UPM, we have demonstrated differences in host-virus interactions dependent on culture environment using mCMV as a model. Based on our studies, we conclude that the 3-D culture environment promotes expansion and prolongation of inter-chromosomal VRCs upon mCMV infection. Although the density of the extracellular matrix would be expected to impede the attachment of virus particles to the host cell, we found that this was not the case, in fact virus infection and replication was enhanced when 3T3 fibroblasts were cultured in a collagen matrix. While other studies of virus infection of cells in a 3-D collagen gels are rare, there is some precedent. Using a GFP labeled Sindbis virus, it was shown that virions penetrated the collagen matrix to infect baby hamster kidney cells.23 Our work supports their study, as we have clearly seen pathological phenotypes of mCMV infected NIH 3T3 fibroblasts cultured in collagen gels.
The immortalized NIH 3T3 cellular phenotype may change significantly in 3-D culture in response to mechano-chemical cues, contributing to the differences we see in this study. Relevant to the differences previously reported in HCV, differentiation of human embryonic stem cells into hepatocytes has been shown under 3-D fluid culture conditions.24 In fact, by 3-D culture, immortalized hepatocytes that have been cultured in a 2-D environment for long periods of time can be induced to switch to a phenotype that more closely matches liver tissue.10 This switch highlights the plasticity of cells and their sensitivity to their microenvironments. It would be interesting to profile the gene expression of NIH 3T3 fibroblasts in 2-D versus 3-D environments to identify candidate host proteins that may interact with virus proteins to account for the differential productivity of infection of 3T3s by mCMV in these contrasting environments.
Using 3-D culture and time-lapse UPM, we have also drawn important conclusions about the relatedness of alpha- and beta-herpes viruses by showing that, similar to what has been reported before for HSV-1, mCMV replication compartments follow the expansion-marginalization model20 and coalesce to form larger replication compartments.
Our study points toward the growing need to study environmental factors resulting in culture dependent host-virus biology. We did not explore how mechanical properties of the ECM may affect host-virus interaction, though recently it has been shown that some cells are more or less sensitive to TGF-β induced apoptosis depending on extracellular matrix stiffness when chemical composition is kept constant.25 In the future, with combined nonlinear optical microscopy and optical coherence microscopy26 which can optically differentiate extracellular matrix components such as collagen, fibrin, and elastin,27,28 we can examine in more detail this intersection of mechano-transduction and immune signaling.29,30
We would like to acknowledge the Texas-UK Collaborative Initiative, National Science Foundation, and Wellcome Trust for supporting this work.
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