Chen Jie-Lin, Zou Chang, Chen Yunfang, Zhu Weimin, Liu Wei, Huang Jianghong, Liu Qisong, Wang Daming, Duan Li, Xiong Jianyi, Cui Jiaming, Jia Zhaofeng, Wang Daping
Shenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen 518035, Guangdong Province, China.
Shenzhen Centre for Sports Medicine and Engineering Technology, Shenzhen 518035, Guangdong Province, China.
Oncotarget. 2017 Aug 24;8(53):91316-91327. doi: 10.18632/oncotarget.20509. eCollection 2017 Oct 31.
The transforming growth factor β1 (TGFβ1) plays an important role in cartilage development. However, whether TGFβ1 stimulates chondrocyte proliferation and cartilage regeneration in osteoarthritis (OA) remains elusive, especially in the context of different treatment and tissue environments. In the present study, we investigated the role of TGFβ1 in human chondrocyte culture , focusing on the morphological change of chondrocytes and the expression of angiogenic factors upon TGFβ1 stimulation. We found increased expression of biomarkers indicating chondrocyte hypertrophy and the chondrocytes aggregated to form networks when they were treated with TGFβ1. DNA microarray analysis revealed significantly increased expression of genes related to blood vessel formation in TGFβ1 treatment group compared to control group. Matrigel assay further demonstrated that chondrocytes had the potential to form network-like structure. These results suggested that TGFβ1 induces the hypertrophic change of chondrocytes culture and induce expression of angiogenic biomarkers. Therefore, application of TGFβ1 for chondrocyte culture in practice should be considered prudentially and targeting TGFβ1 or relevant receptors to block the signaling pathway might be a strategy to prevent or alleviate progression of osteoarthritis.
转化生长因子β1(TGFβ1)在软骨发育中起重要作用。然而,TGFβ1是否能刺激骨关节炎(OA)中的软骨细胞增殖和软骨再生仍不清楚,尤其是在不同治疗和组织环境的背景下。在本研究中,我们研究了TGFβ1在人软骨细胞培养中的作用,重点关注TGFβ1刺激后软骨细胞的形态变化和血管生成因子的表达。我们发现,当用TGFβ1处理时,表明软骨细胞肥大的生物标志物表达增加,且软骨细胞聚集形成网络。DNA微阵列分析显示,与对照组相比,TGFβ1处理组中与血管形成相关的基因表达显著增加。基质胶实验进一步证明软骨细胞具有形成网络样结构的潜力。这些结果表明,TGFβ1可诱导软骨细胞培养物发生肥大变化并诱导血管生成生物标志物的表达。因此,在实践中应用TGFβ1进行软骨细胞培养时应谨慎考虑,靶向TGFβ1或相关受体以阻断信号通路可能是预防或减轻骨关节炎进展的一种策略。