- Open Access
Rb induces a proliferative arrest and curtails Brn-2 expression in retinoblastoma cells
© Cobrinik et al; licensee BioMed Central Ltd. 2006
- Received: 20 July 2006
- Accepted: 12 December 2006
- Published: 12 December 2006
Retinoblastoma is caused by loss of the Rb protein in early retinal cells. Although numerous Rb functions have been identified, Rb effects that specifically relate to the suppression of retinoblastoma have not been defined.
In this study, we examined the effects of restoring Rb to Y79 retinoblastoma cells, using novel retroviral and lentiviral vectors that co-express green fluorescent protein (GFP). The lentiviral vector permitted transduction with sufficient efficiency to perform biochemical analyses. Wild type Rb (RbWT) and to a lesser extent the low penetrance mutant Rb661W induced a G0/G1 arrest associated with induction of p27KIP1 and repression of cyclin E1 and cyclin E2. Microarray analyses revealed that in addition to down-regulating E2F-responsive genes, Rb repressed expression of Brn-2 (POU3F2), which is implicated as an important transcriptional regulator in retinal progenitor cells and other neuroendocrine cell types. The repression of Brn-2 was a specific Rb effect, as ectopic p27 induced a G0/G1 block, but enhanced, rather than repressed, Brn-2 expression.
In addition to Rb effects that occur in many cell types, Rb regulates a gene that selectively governs the behavior of late retinal progenitors and related cells.
- Green Fluorescent Protein
- Green Fluorescent Protein Expression
- Retinoblastoma Cell
- Retinal Progenitor Cell
Retinoblastomas form due to the inactivation of the RB1 gene together with other genetic changes . Whereas RB1 is also inactivated in other tumors, the cells that give rise to retinoblastoma are exceptionally sensitive to Rb loss. Individuals with bilateral retinoblastoma (and presumed germ line RB1 mutations) develop an average of five retinoblastoma foci, generally within their first 2 years [2, 3], but have only ~1% per year likelihood of developing all other tumor types . Moreover, retinoblastoma is largely a human-specific disease. Tumors with histopathological features of retinoblastoma, including photoreceptor but not amacrine differentiation, have been reported for only two individual animals [5, 6] and appear not to form in response to the loss of Rb family proteins in mice [7–10].
Rb has numerous functions that might mediate the suppression of retinoblastoma . Studies in non-retinal cells have shown that Rb can inhibit cell cycle progression through regulation of E2F1 and p27Kip1 [12–14], and may induce a senescence-like response through E2F-dependent or E2F-independent mechanisms [15–17]. In addition, Rb promotes differentiation through interactions with several widely expressed proteins [18, 19], and may both promote differentiation and suppress tumorigenesis by inhibiting Ras . Besides these general effects, Rb promotes osteogenic, adipogenic, thyroid, and melanocytic differentiation through interactions that are specific to the relevant cell types [21–26]. Thus, to understand how Rb suppresses retinoblastoma, it may be necessary to identify the cell type-specific functions of Rb in the cells that give rise to retinoblastoma tumors.
At present, the cell type that gives rise to retinoblastoma has not been identified. It was proposed that retinoblastomas arise from a primitive neuroectodermal cell , such as a retinal progenitor cell (RPC) or a transition cell that fails to arrest in Rb's absence during early differentiation . More recent evidence suggests a possible origin from post-mitotic cone precursors . However, defining Rb's tumor suppressor role in any of these cell types is problematic, as human retinal cells are poorly suited to growth and manipulation in vitro, and as Rb's tumor suppressor role may not be replicated in vivo, in mouse models. As an alternative to working with the retinoblastoma cell of origin, insight into Rb's role may be gained by examining the effects of restoring Rb to retinoblastoma cells. While signaling in such cells may differ to some extent from that in the cell of origin, cell type-specific retinoblastoma suppressor functions of Rb seem more likely to be manifested in retinoblastoma cells than in other available cell types.
The effect of restoring Rb to retinoblastoma cells was first examined soon after the RB1 gene was cloned. When Rb was restored using Murine leukemia virus (MLV)-based retroviral vectors, transduced cells were analyzed after >4 weeks of selection and displayed either modestly diminished proliferation [30, 31] or no obvious change in proliferative rate [32–35]. In contrast, when Rb was restored by transfer of chromosome 13 (on which RB1 resides), proliferation was clearly impaired . This suggested that expression of Rb under its normal regulatory sequences conferred a stronger antiproliferative effect than was conferred with MLV-based vectors. However, chromosome transfer is too inefficient to be used to define Rb's acute effects, and cannot be used to compare effects of wild type and mutant Rb proteins.
To define the effects of restoring Rb to retinoblastoma cells, we developed retroviral and lentiviral vectors that co-express Rb and enhanced green fluorescent protein (GFP). As MLV-based retroviral vectors have a propensity to be silenced by trans-acting factors and DNA methylation, we used murine stem cell virus (MSCV) and lentivirus vectors that have diminished silencing [37, 38]. Use of the GFP marker permitted the acute effects of Rb to be observed in the absence of antibiotic selection of transduced cells, and permitted the efficiency of transduction to be determined prior to biochemical analysis. These studies demonstrate that several of the Rb effects that have been observed in other cell types are also manifested in retinoblastoma cells. In addition, they identify an Rb-regulated gene that may have a crucial role in retinal cell proliferation.
Restoration of Rb to Y79 cells using the MSCV-GFP retroviral vector
Viral supernatants were combined with Y79 cells, and infection monitored by flow cytometry. GFP+ cells were first detected ~30 h after infection, and peaked at 44 h, typically in 10–20% of cells. At three days after infection, western blotting indicated that similar levels of RbWT and RbΔ21, and slightly higher levels of Rb661W, were produced (Figure 1B).
Antiproliferative effect of retrovirus-transduced Rb
To determine whether restoring Rb with the MSCV-GFP vector affected Y79 proliferation, the percentage of GFP+ cells was determined at various times after infection and normalized to that at 44 h (Figure 1C). The proportion of GFP+ cells remained constant in cultures transduced with MSCV-GFP, indicating that transduced and untransduced cells proliferated at similar rates. In contrast, the proportion of GFP+ cells rapidly declined after transduction with MSCV-GFP-RbWT, suggesting that proliferation of Rb-transduced cells was impaired.
Cultures that were transduced with the low penetrance mutant Rb661W and the tumor-derived mutants RbΔ21 and RbΔ22 displayed an intermediate decline in GFP+ cells (Figure 1C and data not shown). To determine whether this decline required expression of mutant Rb protein, Y79 cells were transduced with MSCV-GFP-Rb76t, which encodes a truncated and apparently unstable product . As Rb76t-transduced cultures displayed a similar decline in GFP+ cells (Figure 1D), the decline observed with each mutant was likely due to a cis effect of RB1 sequences that resulted in silencing of GFP expression.
To better define the anti-proliferative effect of RbWT, transduced cultures were stained with propidium iodide and the cell cycle profile of GFP+ cells examined. RbWT, but not Rb661W or RbΔ21, increased the proportion of GFP+ cells in G0/G1 and reduced the proportions in S and G2/M (Figure 1E). To our knowledge, this is the first demonstration that restoration of Rb alters the cell cycle profile of retinoblastoma cells. RbWT but none of the Rb mutants also increased Y79 cell size, as measured by immunocytochemical staining and the flow cytometry forward scatter parameter (Figure 1F and data not shown).
Culture of Rb-transduced cells selects for low Rb expression
Restoration of Rb using concentrated retroviral and lentiviral vectors
Antiproliferative effect of lentivirus-transduced RbWT and Rb661W
At 60 h after lentiviral transduction, RbWT induced an accumulation in G0/G1 similar to that induced with retroviral transduction (Figure 3C). Lentiviral transduction of Rb661W also induced an accumulation in G0/G1, though to a lesser extent than RbWT. The ability of Rb661W to elicit a cell cycle block after lentiviral but not retroviral transduction was most likely due to higher levels of Rb661W obtained with the EF1α promoter and a higher multiplicity of infection.
Effect of Rb on gene expression
Gene expression effects of retroviral Rb transduction
Probe Set Accession #
Ribonuc. Reductase M1
Ribonuc. Reductase M2
We next sought to identify additional Rb-regulated genes. One of the most strongly down-regulated genes in the microarray analysis was Brn-2 (POU3F2), with a ~20-fold reduction in signal (Table 1). This effect was confirmed with qRT-PCR analysis of lentivirus-transduced cells, in which RbWT repressed Brn-2 by ~90% (Figure 5A). Moreover, Rb661W down-regulated Brn-2 by 50%, while RbΔ21 and Rb76t had no effect. Rb's regulation of Brn-2 was of interest because Brn-2 functions as an oncogene in melanoma cells and is implicated in the control of Chx10 and other genes that are expressed in RPCs [46, 47]. To determine whether this effect indirectly resulted from Rb-induced cell cycle arrest or p27 expression, we examined Brn-2 expression after p27 transduction. Ectopic p27 increased the proportion of cells in G0/G1 (Figure 4B), but induced rather than diminished Brn-2 expression (Figure 5B). This implies that Rb does not repress Brn-2 through its induction of p27, nor by inducing a G0/G1 arrest.
In summary, Rb not only down regulated E2F-responsive genes, which are thought to have general, cell type-independent functions. Rb also down regulated Brn-2, which is particularly important to the regulation of gene expression in RPCs.
Retinoblastoma has long served as a paradigm for cancers that develop due to the loss of a tumor suppressor protein . However, despite that the Rb tumor suppressor was identified 20 years ago, the means by which Rb suppresses this tumor have not been established. In the current study, we examined the effect of restoring Rb to retinoblastoma cells. Our rationale was that Rb might perform functions in retinoblastoma cells that it does not display in other available cell types, and which may relate to Rb's role in the retinoblastoma cell of origin. As the retinoblastoma cell of origin has not been identified, and cell types that are candidates for the cell of origin are not easily manipulated, retinoblastoma cells may serve as the best available setting in which to detect Rb functions that specifically relate to the suppression of this tumor.
Earlier attempts to define Rb's effects in retinoblastoma cells may have been hampered by an inability to efficiently express Rb and thus examine its acute effects. The current study surmounted this obstacle by marking the Rb expression vectors with GFP. This approach revealed that Rb inhibited proliferation, induced a G0/G1 arrest, and increased cell size, similar to Rb's effects in other cell types. Moreover, the studies showed that Rb's anti-proliferative effect was masked when analyzed several weeks after infection, due to the outgrowth of cells that had low Rb levels. This implies that prior studies that failed to demonstrate an antiproliferative effect of Rb after a selection period may have analyzed cells that had ineffective levels or Rb expression. The firm demonstration that Rb inhibits retinoblastoma proliferation validates efforts to restore Rb function as a therapeutic approach . However, our results also revealed that a threshold level of Rb was required to inhibit Y79 proliferation in vitro. Whether a similar Rb level is needed to inhibit growth of retinoblastoma tumors in vivo remains to be established.
The Rb-induced G0/G1 arrest was associated with increased expression of p27 and decreased expression of E2F-responsive genes, as previously observed in other cell types. In osteosarcoma cells, the induction of p27 preceded the decline in proteins encoded by E2F-responsive genes, and was needed for Rb to rapidly induce a cell cycle block . To date, it has not been possible to determine whether the up-regulation of p27 is required for Rb to arrest Y79 cells, as p27 knockdown did not preclude the induction of p27 by Rb (data not shown). However, our finding that Rb was more effective than p27 in inducing a G0/G1 arrest suggests that Rb inhibits Y79 proliferation at least in part through a p27-independent process, such as by repressing cyclin E2 and other E2F-responsive genes. Notably, the low penetrance mutant Rb661W also induced a G0/G1 block, p27 expression, and down-regulation of cyclin E, albeit to a lesser extent than RbWT. This is consistent with the ability of Rb661W to induce a proliferative arrest via p27 in osteosarcoma cells , and with evidence that Rb661W may regulate E2F-responsive genes through an interaction with E2F2 .
In addition to Rb's effect on E2F-regulated genes, Rb strongly repressed Brn-2. This effect is notable in light of evidence that Brn-2 is highly expressed small cell lung cancers , which like retinoblastomas generally lack Rb , and in light of evidence that Brn-2 functions as an oncogene in melanoma cells [46, 52]. Thus, the finding that Rb represses Brn-2 raises the possibility that deregulation of Brn-2 contributes to retinoblastoma tumorigenesis.
During retinal development, Brn-2 is expressed in intermediate and late RPCs as well as in certain post-mitotic cells . Brn-2 may have a widespread transcriptional role in RPCs, as it binds the promoters of the characteristic RPC genes, Chx10 and Nestin, and may bind related promoter sites in Cyclin D1 and Pax6 . In cortical development, Brn-2 is similarly expressed in late progenitors, and is required in combination with Brn-1 for late progenitor cell proliferation . These findings suggest that Brn-2 may promote the expression of genes that maintain late progenitor cell proliferation, and that deregulation of Brn-2 in response to Rb loss may elicit aberrant expression of such genes, increased proliferation, and retinoblastoma tumorigenesis. Alternatively, as Rb is also expressed in post-mitotic retinal cells , Rb-mediated repression of Brn-2 may contribute to the suppression of retinoblastoma in post-mitotic retinal precursors.
Rb was expressed in Y79 cells using novel retroviral and lentiviral vectors. Rb induced a G0/G1 arrest, expression of p27KIP1, and repression of E2F-responsive genes such as cyclin E1 and cyclin E2, similar to Rb's effects in other cell types. In addition, Rb decreased expression of Brn-2, which selectively regulates gene expression in RPCs and related cells. Thus, in addition to Rb's cell type-independent effects, Rb regulates genes that control transcription in the developing retina.
MSCV-GFP was constructed by replacing the HindIII-ClaI fragment of MSCV-Puro (Clontech) with a HindIII-NotI fragment from pEGFP-N2 (Clontech). To produce MSCV-GFP derivatives, BamHI-StuI fragments from pSVE-hRBWT, pSVE-hRBΔ22 , pSVE-hRB661W [DC unpublished data, 40], and pSVE-Rb76t  were inserted to the BglII-HpaI sites of MSCV-GFP. Similarly, MSCV-Puro-RbWT was produced by inserting the pSVE-hRBWT BamHI-StuI fragment in the MSCV-Puro BglII-HpaI site. MSCV-GFP-RbΔ21 was produced by replacing an MluI-MfeI fragment of MSCV-GFP-RbWT with the corresponding sequence from pGST-RbΔ21 .
BE-GFP was produced by replacing the EcoRV-SalI fragment of MA1, containing a PGK-TrkA cassette , with the polylinker sequence 5'-GGGGCTAGCTCTAGAACGCGTCGTACGACTCGAGTGTTTAAAC-3', and inserting an EF1αpromoter fragment between the polylinker NheI-XbaI sites. RbWT, Rb661W, RbΔ21, and Rb76t cDNAs were transferred as BssHII-BsrGI fragments from MSCV-GFP to the BE-GFP MluI-BsiWI sites. p27KIP1 cDNA was transferred as a KpnI-XbaI fragment from cDNA3-p27 (kindly provided by A. Koff) to the corresponding BE-GFP sites.
Cell growth, virus production, infection, and Y79 sublines
Y79 cells were obtained from the ATCC and cultured in RPMI 1640, 10% fetal calf serum (FCS), penicillin, streptomycin, and L-glutamine, in a humidified 5% CO2 incubator. Retroviral supernatants used for direct infections were made by CaPO4-mediated co-transfection of Bing producer cells with the indicated MSCV-GFP constructs and pCL-Ampho . Concentrated retrovirus was produced by CaPO4-mediated co-transfection of GP2 cells (Clontech) with MSCV-GFP constructs and pVSVg . Lentivirus was produced using Lipofectamine 2000 (InVitrogen) to co-transfect 293T cells with the viral vector, pVSVg, and pΔ8.91 DNAs . Cell supernatants were passed through 0.45 μm cellulose acetate filters 48 h after transfection. Virus was concentrated by centrifugation at 25,000 rpm for 90 min in a SW28 rotor, and suspended in 50 mM Tris, pH 7.8, 130 mM NaCl, and 1 mM EDTA. For infections, Y79 cells were plated at 2 × 106 cells per ml and combined with an equal volume of producer cell supernatants, or with up to 0.5 volume of concentrated virus, at 6 μg/ml polybrene. As MSCV-GFP titers were ~10-fold higher than for Rb derivatives, MSCV-GFP supernatants were diluted 10-fold prior to infection.
Cells transduced with MSCV-Puro or Rb derivatives were selected with 1.5 μg/ml puromycin for 11 days, and re-infected with MSCV-GFP and Rb derivatives 20 days after the initial infection.
Analysis of infected cells
GFP expression and forward scatter were determined using a Becton-Dickenson FACSCaliber and CellQuest Software. Cell cycle positions of retrovirus-transduced cells were determined by fixing in 0.75% paraformaldehyde (PFA) for 30 min at 22°C, washing in PBS + 3% FCS, fixing in 70% ethanol at -20°C, staining in 0.05 mg/ml propidium iodide, 0.6% Nonidet-P40 in PBS, and 1 mg/ml RNAse A, and gating on diploid GFP+ cells. Cell cycle positions of lentivirus-transduced cells were determined as above but without PFA fixation or GFP gating.
For immunofluorescent detection of Rb, Y79 cells were attached to poly-L-lysine coated slides, fixed in 4% PFA for 10 min and stained with anti-Rb antibody G3-245 (1:200, Becton-Dickenson) and Cy3-conjugated donkey anti-mouse. For immunoblotting, lysates were separated and immunoblotted to Hybond-P and probed using ECL-Advance (Amersham), with mouse anti-Rb G3-245 (1:1,200), rabbit anti-p27 (1:150, SantaCruz sc-528), and rabbit anti-α-actin (1:1,000, Sigma A2066). To compare Rb expression after retroviral infection, infected cell lysates were combined with mock-infected cell lysates to normalize for the proportion of GFP+ cells.
RB1 cDNA expressed following retroviral transduction was detected by RT-PCR with forward primer 5'-GCTTGAGTTTGAAGAAACAGAAGAACC and reverse primer 5'-CTTTAGCTAATAAAAATGTGATCCAAGAAACTT, and with a GAPDH control.
Gene expression analysis
RNA was prepared 60 h after lentivirus infection or after retrovirus infection followed by FACS enrichment to >97% GFP+ cells. In the latter case, cells were suspended in Buffer RLT (Qiagen) within 10 min after sorting. RNA was prepared using RNeasy (Qiagen) including on-column DNAse digestion, and RNA quality confirmed by Agilent BioAnalyzer. For microarray analysis, 10 ng of each RNA was used to prepare probes with the Ovation Biotin Amplification System (Novogen), and probing Affymetrix U133 Plus 2.0 GeneChip. For real-time quantitative PCR (RT-qPCR), oligo dT-primed cDNA was prepared from 750 ng RNA and ImProm-II reverse transcriptase (Promega), and cDNA transcribed from 5 ng of RNA subjected to RT-qPCR using iTaq SYBR Green Supermix (Bio-Rad), and normalized to β-actin RNA measured by Taqman (Applied Biosystems). PCR primers were for cyclin E1 (forward 5'-CGTGCGTTTGCTTTTACAGA, reverse 5'-AGCACCTTCCATAGCAGCAT); cyclin E2 (forward 5'-CCTCCATTGTGAGATAAGGACA, reverse 5'-GCCTATGTACAGCAAGTTTTCA); Brn-2 (forward 5'-CAGAGAGATGGCAAGCACTG, reverse 5'-TCAGGAAGCTGCATTTTGTG); and HSP70A1B (forward 5'-CCGAGAAGGACGAGTTTGAG, reverse 5'-GCAGCAAAGTCCTTGAGTCC).
We thank Drs. L. Naldini, P. Hinds, W. Kaelin, F. Kaye, and A. Koff for DNA constructs, and Dr. Jenny Xiang of Weill Medical College Microarray Core Facility for assistance with microarray analysis. This work was supported by grants from the C.V. Starr Foundation, the Fred Gluck Foundation, Research to Prevent Blindness, and the New York Community Trust.
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