Liao Junyi, Hu Ning, Zhou Nian, Lin Liangbo, Zhao Chen, Yi Shixiong, Fan Tingxu, Bao Wei, Liang Xi, Chen Hong, Xu Wei, Chen Cheng, Cheng Qiang, Zeng Yongming, Si Weike, Yang Zhong, Huang Wei
Department of Orthopaedic Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Department of Radiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
PLoS One. 2014 Feb 13;9(2):e89025. doi: 10.1371/journal.pone.0089025. eCollection 2014.
Bone morphogenetic protein 2 (BMP2) is one of the key chondrogenic growth factors involved in the cartilage regeneration. However, it also exhibits osteogenic abilities and triggers endochondral ossification. Effective chondrogenesis and inhibition of BMP2-induced osteogenesis and endochondral ossification can be achieved by directing the mesenchymal stem cells (MSCs) towards chondrocyte lineage with chodrogenic factors, such as Sox9. Here we investigated the effects of Sox9 on BMP2-induced chondrogenic and osteogenic differentiation of MSCs. We found exogenous overexpression of Sox9 enhanced the BMP2-induced chondrogenic differentiation of MSCs in vitro. Also, it inhibited early and late osteogenic differentiation of MSCs in vitro. Subcutaneous stem cell implantation demonstrated Sox9 potentiated BMP2-induced cartilage formation and inhibited endochondral ossification. Mouse limb cultures indicated that BMP2 and Sox9 acted synergistically to stimulate chondrocytes proliferation, and Sox9 inhibited BMP2-induced chondrocytes hypertrophy and ossification. This study strongly suggests that Sox9 potentiates BMP2-induced MSCs chondrogenic differentiation and cartilage formation, and inhibits BMP2-induced MSCs osteogenic differentiation and endochondral ossification. Thus, exogenous overexpression of Sox9 in BMP2-induced mesenchymal stem cells differentiation may be a new strategy for cartilage tissue engineering.
骨形态发生蛋白2(BMP2)是参与软骨再生的关键软骨生成生长因子之一。然而,它也具有成骨能力并引发软骨内骨化。通过用软骨生成因子(如Sox9)引导间充质干细胞(MSC)向软骨细胞谱系分化,可以实现有效的软骨生成以及对BMP2诱导的成骨和软骨内骨化的抑制。在此,我们研究了Sox9对BMP2诱导的MSC软骨生成和成骨分化的影响。我们发现,Sox9的外源性过表达增强了体外BMP2诱导的MSC软骨生成分化。此外,它还抑制了体外MSC的早期和晚期成骨分化。皮下干细胞植入表明,Sox9增强了BMP2诱导的软骨形成并抑制了软骨内骨化。小鼠肢体培养表明,BMP2和Sox9协同作用刺激软骨细胞增殖,且Sox9抑制BMP2诱导的软骨细胞肥大和骨化。本研究有力地表明,Sox9增强了BMP2诱导的MSC软骨生成分化和软骨形成,并抑制了BMP2诱导的MSC成骨分化和软骨内骨化。因此,在BMP2诱导的间充质干细胞分化中,Sox9的外源性过表达可能是软骨组织工程的一种新策略。