Transforming Growth Factor-β Stimulates Cyclin D1 Expression through Activation of β-Catenin Signaling in Chondrocytes*

Transforming growth factor-β (TGF-β) plays an essential role in chondrocyte maturation. It stimulates chondrocyte proliferation but inhibits chondrocyte differentiation. In this study, we found that TGF-β rapidly induced β-catenin protein levels and signaling in murine neonatal sternal primary chondrocytes. TGF-β-increased β-catenin induction was reproduced by overexpression of SMAD3 and was absent in Smad3-/- chondrocytes treated with TGF-β. SMAD3 inhibited β-transducin repeat-containing protein-mediated degradation of β-catenin and immunoprecipitated with β-catenin following TGF-β treatment. Both SMAD3 and β-catenin co-localized to the nucleus after TGF-β treatment. Although both TGF-β and β-catenin stimulated cyclin D1 expression in chondrocytes, the effect of TGF-β was inhibited with β-catenin gene deletion or SMAD3 loss of function. These results demonstrate that TGF-β stimulates cyclin D1 expression at least in part through activation of β-catenin signaling.

μg/ml ascorbic acid, pH 7.1). The cells were counted and plated at the appropriate density. To remove any remaining fibroblasts, 24-h cultures were treated with 0.05% trypsin for 1 min to lift the fibroblasts from the culture dish while allowing the chondrocytes to remain attached. A similar procedure was used for chondrocyte isolation from β-catenin flox/flox mice (8) and βcatenin reporter TOPGAL transgenic mice, in which a β-galactosidase gene is under the control of a lymphoid enhancer factor/T cell factor (TCF)-and β-catenin-inducible promoter. In these transgenic mice, TOPGAL expression is directly stimulated by a stabilized form of β-catenin (9). The chondrocyte cell line RCJ3.1C5. 18 (C5.18) was cultured in α-minimal essential medium containing 10% FBS. In cyclin D 1 reporter and Western blot assays, all cells were synchronized for 3 days in serum-free medium prior to different treatments.

Adenovirus Production and Infection
The full-length mouse β-catenin cDNA was cloned into the TOPO entry vector using the Gateway system (Invitrogen). By LR reaction, a β-catenin insert was subcloned into the ViraPower™ adenoviral expression vector. The plasmid was linearized using PacI and transiently transfected into 293A cells. After several cycles of amplification, the adenovirus was purified using the CsCl binding method. Ad5-CMV-Cre-GFP and Ad5-CMV-enhanced GFP were purchased from the Baylor College of Medicine. Infection (multiplicity of infection of 10) lasted for 24 h, and cells were allowed to recover for 48 h prior to treatments. β-Catenin flox/flox chondrocytes were infected with Ad5-CMV-Cre-GFP for 24 h and recovered in full medium for 48 h. Ad5-CMV-enhanced GFP was used in the same way as a control.

β-Galactosidase Activity Assay
TOPGAL chondrocytes were plated for 24 h. TGF-β (1 ng/ml) was added to cultures in serumfree medium for 24 h. β-Galactosidase activity was measured with a luminescent βgalactosidase detection kit (BD Biosciences) on a luminometer (Opticom 1, MGM Instruments, Inc., Hamden, CT). Each cell preparation was tested in triplicate, and the values were standardized by protein concentrations. The results are presented as the means ± S.E.

Transfections and Luciferase Assay
Transient transfection was performed using a Targefect F-2 reagent kit (Targeting Systems, Santee, CA). To increase the transfection efficiency, Virofect provided in the kit was added to all reactions. The transfection complex was formed after incubation at 37 °C for 20 min. At the same time, chondrocytes were pretreated with hyaluronidase (200 ng/ml; Sigma) at 37 °C for 30 min. The transfection complex was then added to cell culture dishes containing Dulbecco's modified Eagle's medium with 10% FBS. The following plasmids were transfected into chondrocytes for 12 h before treatments: TOPflash and FOPflash reporter plasmids (a gift from Dr. Jennifer Westendorf, Mayo Clinic College of Medicine, Rochester, MN), the cyclin D 1 promoter (-1745CD1-Luc, a gift from Dr. Phyllis LuValle, University of Florida, Gainesville, FL), β-catenin S33Y (constitutively active β-catenin, a gift from Dr. Kenneth Kinzler, The Johns Hopkins University Medical Institutions, Baltimore, MD) (10), F-SMAD3 (a gift from Dr. Yin Sun, University of Rochester, Rochester, NY), and inhibitor of β-catenin and TCF (ICAT; a gift from Dr. Tetsu Akiyama, University of Tokyo, Japan) (11,12). An SV40-Renilla luciferase construct was cotransfected with the above firefly reporters to standardize results for transfection efficiency. Luciferase activity in the cell lysate was determined using a luminometer (Opticom 1). Murine β-transducin repeat-containing protein (β-TrCP) cDNA was amplified by real-time PCR using template RNA extracted from 2T3 osteoblast precursor cells and then cloned into the p3XFLAG-CMV vector (Sigma). The nucleotide sequence was verified by sequencing the entire cDNA.

Western Blotting
Chondrocytes were lysed in Golden lysis buffer supplemented with protease inhibitor (Roche Applied Science), 1 mM sodium orthovanadate, 1 mM ethylene glycol bis(β-aminoethyl ether), 1 mM sodium fluoride, and 1 μM microcysteine (Sigma). The protein concentration was determined using a Coomassie Plus protein assay kit (Pierce). The protein extracts (10 μg) were separated using NuPAGE™ Bis-Tris gels (Invitrogen). After transfer to a polyvinylidene difluoride membrane (PerkinElmer Life Sciences) and blocking with 5% milk, the blots were probed with the following mouse monoclonal antibodies overnight at 4 °C: anti-β-catenin (Upstate, Lake Placid, NY), anti-active β-catenin (Upstate), and anti-cyclin D 1 (Cell Signaling Technology, Beverly, MA). Anti-β-actin monoclonal antibody (Sigma) at a dilution of 1:8000 was used to confirm equal protein loading. Horseradish peroxidase-conjugated secondary antibodies (Bio-Rad) were then applied to the membrane and incubated for 60 min. The immune complexes were detected using SuperSignal West Femto maximum sensitivity substrate (Pierce). For multiple detection of different antibodies in the same membrane, we used ReBlot Plus strong antibody stripping solution (Chemicon International, Inc., Temecula, CA).

Double Immunofluorescence Labeling and Confocal Microscopy
C5.18 chondrogenic cells (13) were plated in 2-well chamber slides (2000 cells/well; Nalgene Nunc International, Rochester, NY) for 24 h and then treated with TGF-β (1 ng/ml) for 4 h. After washes with PBS, the cells were fixed with acetone/methanol (1:1) at 4 °C for 30 min. Nonspecific binding was blocked by incubation with PBS containing 10% normal goat serum at room temperature for 1 h. After excess serum was removed, mouse anti-β-catenin and rabbit anti-SMAD3 antibodies diluted to 1:50 in PBS containing 10% goat serum and 0.1% saponin (Research Organics, Inc., Cleveland, OH) were applied to slides and incubated overnight at 4°C . After thorough washes with PBS, the slides were incubated in the dark for 1 h with fluorescein isothiocyanate (FITC)-conjugated goat anti-mouse and tetramethylrhodamine isothiocyanate (TRITC)-conjugated goat anti-rabbit secondary antibodies (Jackson ImmunoResearch Laboratories, Inc., West Grove, PA) diluted 1:100 in PBS containing 0.1% saponin and 10% goat serum. The slides were then rinsed with tap water for 30 min and mounted with VECTASHIELD medium (Vector Laboratories, Burlingame, CA). Immunofluorescence was detected using a Zeiss microscope with different filters. Similarly, after double labeling, specimens were viewed either through a ×40 objective on a Nikon Diaphot inverted fluorescence microscope or through a ×100 oil immersion objective on a Leica TCS SP confocal laser scanning microscope equipped with two lasers working simultaneously with excitation wavelengths of 543 and 488 nm to detect TRITC and FITC, respectively. The confocal three-dimensional data were processed using the Leica confocal LCS software program.

Real-time PCR
Total RNA was extracted from cultures using an RNeasy kit (Qiagen Inc., Valencia, CA). 1 μg of RNA was reversed-transcribed using an Advantage RT-for-PCR kit (BD Biosciences).
Real-time PCR was performed using the Rotor-Gene real-time DNA amplification system (Corbett Research, New South Wales, Australia) and the fluorescent dye SYBR Green I to monitor DNA synthesis (SYBR Green PCR Master Mix, Applied Biosystems, Foster City, CA). The primers used in this study were as follow: β-actin, 5′-TGT TAC CAA CTG GGA CGA CA and 3′-CTG GGT CAT CTT TTC ACG GT; and cyclin D 1 ,5′-GGC ACC TGG ATT GTT CTG TT and 3′-CAG CTT GCT AGG GAA CTT GG. The PCR protocol included a denaturation step at 95 °C for 10 min, followed by 40 cycles of denaturation at 95 °C for 20 s, annealing for 20 s, and extension at 72 °C for 30 s. Detection of the fluorescent product was carried out at the end of the 72 °C extension period. PCR products were subjected to a melting curve analysis, and the data were analyzed and quantified with the Rotor-Gene analysis software. Dynamic tube normalization and noise slope correction were used to remove background fluorescence. Each sample was tested at least in triplicate and repeated for three independent cell preparations.

In Vivo 5-Bromo-2′-deoxyuridine (BrdUrd) Labeling and Histology
Concentrated BrdUrd solution (Zymed Laboratories Inc.) was injected into the peritoneal cavities of 4-day-old neonatal mice (1 ml/100 g of body weight). Mice were killed 4 h later, and lower limb samples centered at knee joints were harvested and processed. Decalcified tissue sections were labeled using a BrdUrd staining kit (Zymed Laboratories Inc.), counterstained with hematoxylin, and mounted with Permount. All BrdUrd-positive chondrocytes in the growth plate were counted, and at least three samples from each group were used.

In Vitro BrdUrd Labeling and Flow Cytometry
BrdUrd (10 μM) was added to cultures containing primary chondrocytes and incubated for 2 h. The cells (∼2 × 10 6 ) were trypsinized, washed with PBS, and fixed with 75% ethanol at 4 °C for 24 h. On the day of flow cytometry, the cells were washed with PBS and incubated with pepsin solution for 30 min. After spinning and decanting, the cells were resuspended with 1 ml of PBS containing 0.5% FBS and 0.5% Tween 20. Then, the cells were incubated with 1 ml of PBS containing 2% FBS at room temperature for 30 min. FITC-conjugated anti-BrdUrd antibody (Roche Applied Science) was added to the above solution and incubated for 60 min in the dark. After washes, cells were treated with RNase A (1 mg/ml) at room temperature for 30 min. Finally, cells were labeled with propidium iodide (20 μg/ml in PBS) for 10 min at room temperature, filtered through 37-μm mesh, and loaded onto a FACSCanto flow cytometer (BD Biosciences).

Statistics
Statistical comparisons were made between groups using either analysis of variance or Student's t test as appropriate. p values <0.05 were considered significant and are denoted in the figures.

TGF-β Stimulates β-Catenin Signaling
Initial experiments examined β-catenin signaling in C5.18 cells and in primary chondrocytes isolated from the sterna of TOPGAL transgenic mice. Cotransfection of the TOPflash reporter with the constitutively active β-catenin expression plasmid β-catenin S33Y in C5.18 cells resulted in stimulation of reporter activity. Similarly, infection of TOPGAL chondrocytes with Ad-β-catenin resulted in increased β-galactosidase activity ( Fig. 1, a and b).
To determine whether TGF-β activates β-catenin signaling in chondrocytes, we examined the effect of TGF-β (1 ng/ml) on β-galactosidase activity in primary chondrocytes isolated from TOPGAL transgenic mice and found that TGF-β stimulated β-galactosidase activity in a dosedependent manner (Fig. 1c). To investigate whether TGF-β increases β-catenin protein levels in chondrocytes, we treated C5.18 cells with TGF-β (1 ng/ml) for different periods of time and examined changes in β-catenin protein levels by Western blot analysis. TGF-β significantly increased the protein levels of the total and active non-phosphorylated forms of β-catenin in a time-dependent manner. TGF-β increased β-catenin protein levels within 15 min, and its maximum effect was achieved at the 2-h time point after TGF-β treatment (Fig. 1d). In contrast, TGF-β had no effect on β-catenin mRNA expression in these cells (data not shown). These results suggest that TGF-β activates β-catenin signaling by increasing β-catenin protein levels in chondrocytes.

TGF-β Activates β-Catenin Signaling through SMAD3
To determine whether TGF-β-regulated β-catenin protein levels are mediated by SMAD3, we examined the steady-state protein levels of β-catenin in Smad3 knock-out chondrocytes. Cell lysates were extracted from sternal chondrocytes derived from wild-type and Smad3 knockout mice, and changes in β-catenin protein levels were detected by Western blotting using antiβ-catenin monoclonal antibody. The results showed that both total and active nonphosphorylated β-catenin levels were significantly reduced in Smad3-deficient chondrocytes compared with wild-type chondrocytes (Fig. 2a). In addition, the cyclin D 1 protein level was also reduced in Smad3 -/chondrocytes (Fig. 2a). To further determine whether TGF-β activates β-catenin signaling through SMAD3, we transfected the TOPflash reporter into chondrocytes isolated from wild-type or Smad3 knock-out mice and treated these cells with TGF-β (1 ng/ ml). TGF-β stimulated TOPflash reporter activity in wild-type but not Smad3 knock-out chondrocytes (Fig. 2b). To further determine the role of SMAD3 in β-catenin signaling, the SMAD3 expression plasmid was cotransfected with the β-catenin reporter into C5.18 cells. Although transfection of SMAD3 alone significantly increased β-catenin reporter activity, cotransfection of SMAD3 with β-catenin S33Y only slightly enhanced β-catenin-induced TOPflash reporter activity (Fig. 2c), suggesting that overexpression of β-catenin may have already achieved a maximum level of reporter induction. These results demonstrate that TGFβ activates β-catenin signaling through SMAD3 in chondrocytes.

SMAD3 Interacts with β-Catenin in Chondrocytes
To determine whether SMAD3 directly interacts with β-catenin in chondrocytes, we performed immunoprecipitation assays. C5.18 chondrocytes were cultured in the presence or absence of TGF-β for 30 min, and cell lysates were extracted and subjected to immunoprecipitation using anti-SMAD3 antibody or anti-His control antibody, followed by Western blot analysis using anti-β-catenin antibody. A weak interaction between SMAD3 and β-catenin was detected in the absence of TGF-β. In contrast, a strong interaction between SMAD3 and β-catenin was detected in the presence of TGF-β (Fig. 2d, upper panels). In contrast, SMAD2 did not interact with β-catenin in C5.18 cells (data not shown). These results suggest that β-catenin may interact mainly with phospho-SMAD3 upon TGF-β treatment in chondrocytes.

β-Catenin Induces Cyclin D 1 Expression in Chondrocytes
We then determined the effect of β-catenin on cyclin D 1 gene transcription and expression in chondrocytes. C5.18 chondrocytes were cotransfected with the β-catenin S33Y plasmid and the 1.7-kb human cyclin D 1 promoter. Overexpression of β-catenin S33Y stimulated cyclin D 1 promoter activity in C5.18 chondrocytes (Fig. 5a). Cyclin D 1 protein expression was also increased when C5.18 chondrocytes were infected with Ad-β-catenin (Fig. 5b). In contrast, C5.18 chondrocytes cotransfected with the cyclin D 1 promoter and ICAT had reduced cyclin D 1 promoter activity (Fig. 5c). To further determine the role of β-catenin in cyclin D 1 expression in chondrocytes, we isolated primary chondrocytes from β-catenin-loxP mice (8) and infected these cells with Ad-Cre. Cells infected with Ad-GFP were used as a control. The results showed that, in Ad-Cre-infected chondrocytes, cyclin D 1 expression was significantly reduced compared with Ad-GFP-infected cells (Fig. 5d). Taken together, these results demonstrate that β-catenin plays an important role in cyclin D 1 expression in chondrocytes.

TGF-β Stimulates Cyclin D 1 Expression and Cell Growth through SMAD3
To determine the role of TGF-β in chondrocyte cell growth, we examined changes in cell proliferation in Smad3 knock-out mice and found that BrdUrd-positive chondrocytes in the proliferating zone of the growth plate were decreased by ∼30% (Fig. 6, a-e). This finding was confirmed by an in vitro BrdUrd labeling experiment using primary chondrocytes isolated from Smad3 knock-out mice and their wild-type littermates. The results showed that BrdUrdpositive cells were significantly reduced in Smad3 knock-out chondrocytes, independent of serum starvation (Fig. 6f). In Smad3 knock-out chondrocytes, expression of cyclin D 1 mRNA and protein was significantly decreased (Fig. 2a and Fig. 6g). Taken together, these results indicate that TGF-β stimulates cyclin D 1 expression and cell growth through SMAD3 in chondrocytes.

TGF-β-induced Cyclin D 1 Expression Is Mediated by β-Catenin
Because both TGF-β and β-catenin stimulate cyclin D 1 expression and because TGF-β activates β-catenin signaling in chondrocytes, we hypothesized that TGF-β induces cyclin D 1 expression through activation of β-catenin signaling. To test this hypothesis, primary chondrocytes were isolated from the β-catenin-loxP mice, infected with Ad-Cre or Ad-GFP, and treated with TGFβ. TGF-β stimulated cyclin D 1 expression in Ad-GFP-infected but not Ad-Cre-infected chondrocytes (Fig. 7a). Consistent with these findings, transfection of the constitutively active type I TGF-β receptor (19) increased cyclin D 1 expression, which was completely inhibited by cotransfection of ICAT (Fig. 7b). ICAT is an 82-amino acid protein that interferes with the binding of β-catenin to TCF and inhibits β-catenin/TCF-induced transcription of downstream target genes (11,12). These results strongly suggest that TGF-β regulates cyclin D 1 expression in a β-catenin-dependent manner.

DISCUSSION
TGF-β has been shown to stimulate cyclin D 1 expression and chondrocyte proliferation (2,7,20). A recent study demonstrated that β-catenin controls chondrocyte proliferation and terminal differentiation (21). The interaction of TGF-β and β-catenin signaling in chondrocytes has not been previously described. In this study, we have demonstrated that TGF-β activated β-catenin signaling through SMAD3. SMAD3 directly interacted with β-catenin. TGF-β may increase β-catenin protein levels by preventing β-catenin degradation because TGF-β increased βcatenin protein levels but had no effect on β-catenin mRNA expression. TGF-β lost its ability to induce cyclin D 1 expression when the β-catenin gene was deleted in chondrocytes, suggesting that TGF-β-induced cyclin D 1 expression is mediated by β-catenin in chondrocytes. These findings provide novel insights into the interaction between TGF-β and β-catenin signaling pathways and the regulatory mechanism of chondrocyte proliferation.
TGF-β stimulates cell proliferation through induction of cyclin D 1 (20,2), which is critical for progression through G 1 to S phase of the cell cycle. Regulation of the cell cycle is controlled by a combination of cyclins, cyclin-dependent kinases (Cdks), and Cdk inhibitors, which, together with the retinoblastoma tumor suppressor (Rb), are involved in the tight control of cell cycle machinery. Cdks, in association with their regulatory partners, the cyclins, are key regulators of cell cycle progression. Cdk2-cyclin A/E and Cdk4/6-cyclin D are involved in the G 2 /M transition of the cell cycle (22,23). Cdk4/6-cyclin D promotes the phosphorylation of Rb. Hypophosphorylated Rb proteins are known to inhibit the function of E2F proteins, which promote transcription of factors essential for DNA synthesis (24). Thus, phosphorylation of Rb by Cdk-cyclin D complexes relieves inhibition of Rb on the E2F function, promoting the entry of cells into S phase. In cyclin D 1 knock-out mice, chondrocyte proliferation is inhibited, and the proliferating zone is reduced by >50% in the growth plate, indicating that cyclin D 1 plays a critical role in chondrocyte proliferation (2).
β-TrCP-Skp1 is a ubiquitin-protein isopeptide ligase complex that is involved in β-catenin degradation (14)(15)(16)(17)(18). In this study, we found that β-TrCP-induced β-catenin degradation was reduced in the presence of SMAD3, suggesting that the binding of SMAD3 to β-catenin may protect β-catenin degradation. Skp2 (S phase kinase-interacting protein-2) is a homolog of Skp1 and has been reported to be involved in the ubiquitination of the Cdk inhibitor p27 Kip1 ; in epithelial cells, TGF-β causes cell cycle arrest in part through inhibition of Skp2 and stabilizing p27 Kip1 (25). In contrast to epithelial cells, TGF-β promotes chondrocyte proliferation through activation of cyclin D 1 (Refs. 2 and 19 and this study). TGF-β had no effect on p21 Kip1 expression but slightly increased p27 Kip1 levels in chondrocytes (data not shown), and the effect of TGF-β on Skp2 function in chondrocytes is currently unknown.
It has been reported that TGF-β regulates cyclin D 1 expression through activation of activating transcription factor-2, which directly binds the cyclin D 1 promoter and activates cyclin D 1 gene transcription in chondrocytes (20). Our results indicate that TGF-β also regulates cyclin D 1 gene expression through activation ofβ-catenin signaling. Multiple TCF-binding sites have been identified on the cyclin D 1 promoter (26). These findings suggest that TGF-β may control cyclin D 1 expression through at least two separate pathways and that induction of β-catenin is necessary for TGF-β-induced cyclin D 1 induction. Further studies are required to determine whether β-catenin/TCF interacts with activating transcription factor-2 at the cyclin D 1 promoter.
β-Catenin plays a critical role in chondrocyte development. Although β-catenin suppresses the differentiation of mesenchymal cells into Sox9-expressing chondrocyte precursors (31,32), it promotes chondrocyte maturation in growth plate chondrocytes by stimulating chondrocyte proliferation and increasing chondrocyte marker gene expression. When the β-catenin gene is specifically deleted in Col2a1-expressing chondrocytes, chondrocyte proliferation is decreased, and hypertrophic chondrocyte differentiation is delayed (21). The effect of β-catenin on chondrocyte maturation is regulated by transcription factor SOX9. SOX9 binds the armadillo repeats of β-catenin and inhibits the interaction of β-catenin with TCF (21). Our recent findings demonstrate that Wnt3a stimulates type X collagen expression through activation of bone morphogenetic protein signaling in chondrocytes (33). These observations demonstrate that β-catenin interacts with other transcription factors or signaling pathways during chondrocyte maturation. Although the detailed mechanism of how TGF-β prevents βcatenin degradation and induces β-catenin nuclear translocation requires further investigation, our current findings clearly demonstrate that TGF-β regulates cyclin D 1 expression through activation of β-catenin signaling.
We (6) and others (34) have shown that β-catenin induces prehypertrophic chondrocytes to complete terminal maturation. Overexpression of β-catenin or addition of Wnt3a, which induces the canonical β-catenin signaling pathway, stimulates expression of colX and other maturational markers (6,34). Furthermore, we demonstrated that TGF-β treatment inhibits activation of the TOPflash promoter by β-catenin in chick upper sternal chondrocytes (6). Although these findings seemingly contradict the current observation that TGF-β induces βcatenin signaling through a SMAD3-mediated mechanism, important differences between the culture models likely account for the discrepancy in the findings. The previous work utilized embryonic chick upper sternal chondrocytes (6). These chondrocytes express colX and spontaneously complete maturation and thus are in a relatively differentiated state at the time of harvest (6). Although the murine sternal chondrocytes used in the current experiments respond to BMP-2 and other differentiation signals and are capable of undergoing maturation, under basal conditions, colX expression is absent, and the cells are in a much less mature state and do not undergo spontaneous maturation (35).
It has been established that β-catenin has a complex role during chondrogenesis and subsequent endochondral ossification, and in vivo findings in β-catenin-deficient mice support a role for β-catenin in both proliferation and differentiation (21). In mesenchymal stem cells, β-catenin inhibits chondrogenesis and causes cells to differentiate toward an osteoblast phenotype (32). Interestingly, TGF-β and SMAD3 have been shown to enhance β-catenin signaling in embryonic maxillary mesenchymal cells (36). In prehypertrophic and hypertrophic chondrocytes committed to maturation, β-catenin induces terminal differentiation (6,34). The current findings similarly suggest that, in proliferating and immature chondrocytes, β-catenin acts downstream of TGF-β and functions to stimulate chondrocyte proliferation, consistent with an effect on proliferation in other cell types (37)(38)(39). Thus, a possible explanation of the role of TGF-β signaling in modulating Wnt canonical signaling during cell growth versus differentiation is that SMAD3 enhances β-catenin signaling during cell proliferation but inhibits signaling in more differentiated chondrocytes progressing toward terminal maturation. Although, at a later stage, β-catenin clearly functions to stimulate terminal differentiation, the mechanisms involved in the transition from proliferation to differentiation and the dual role of β-catenin in these processes remain elusive. However, given the current findings, it is likely that interactions with the TGF-β and bone morphogenetic protein signaling pathways are involved.

FIGURE 3. TGF-β induces β-catenin nuclear translocation
a, C5.18 chondrocytes were cultured with or without TGF-β (1 ng/ml). After 4 h of TGF-β treatment, cells were fixed and incubated with either anti-β-catenin or anti-SMAD3 antibody, followed by incubation with either FITC-or TRITC-conjugated secondary antibody. The results showed that treatment with TGF-β induced the nuclear translocation of SMAD3 as well as β-catenin. b, similarly, treated cells were examined under a confocal microscope. In the absence of TGF-β, both β-catenin and SMAD3 stayed in the cytoplasm. Treatment with TGFβ promoted both SMAD3 and β-catenin nuclear translocation and co-localization.

FIGURE 5. β-Catenin induces cyclin D 1 expression in chondrocytes
a, C5.18 chondrocytes were synchronized in serum-free medium for 72 h. The cyclin D 1luciferase (Luc) reporter construct was cotransfected with either the empty vector control (Vect) or β-catenin S33Y (β-cat S33Y ) for 24 h, and luciferase assay was performed. Transfection of β-catenin S33Y increased cyclin D 1 reporter activity by ∼5-fold compared with the empty vector control. b, C5.18 chondrocytes were infected with Ad-GFP or Ad-β-catenin (Ad-βcat) for 24 h. After the medium was changed, cells were cultured in serum-free medium for 72 h. Western blotting showed that overexpression of β-catenin (Ad-β-catenin) increased the protein level of cyclin D 1 in C5.18 chondrocytes. c, C5.18 chondrocytes were synchronized in FIGURE 6. Chondrocyte proliferation is reduced in Smad3 knock-out mice a-d, BrdUrd labeling reagent was injected into the peritoneal cavities of 4-day-old neonatal mice. Mice were killed 4 h later, and hind limbs were harvested. The decalcified tissue sections were stained using a BrdUrd staining kit and counterstained with hematoxylin. a and c, wildtype mice; b and d, Smad3 -/knock-out (KO) mice. e, morphometric analysis revealed that the number of BrdUrd-positive chondrocytes was significant lower in Smad3 -/mice than in wildtype (Wt) mice. f, primary chondrocytes isolated from either wild-type or Smad3-deficient mice were cultured with BrdUrd reagent. After fixation, cells were incubated with FITC-conjugated anti-BrdUrd antibody. The results from flow cytometry showed that the numbers of BrdUrdpositive chondrocytes were reduced in Smad3 -/mice with or without serum starvation. g, primary chondrocytes isolated from either wild-type or Smad3-deficient mice were lysed, and total RNA was extract. After reverse transcription, real-time PCR was performed using cyclin D 1 primers. The results showed that cyclin D 1 mRNA expression was decreased in Smad3 -/chondrocytes.