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音猬因子在旋转细胞培养系统中促进兔骨髓干细胞的软骨形成。

Sonic hedgehog promotes chondrogenesis of rabbit bone marrow stem cells in a rotary cell culture system.

作者信息

Chen Liyang, Liu Gejun, Li Wenjun, Wu Xing

机构信息

Department of Orthopaedics, Tenth People's Hospital of Tongji University, Tongji University, Shanghai, 200072, China.

School of Medicine, Tongji University, Shanghai, 200072, China.

出版信息

BMC Dev Biol. 2019 Aug 12;19(1):18. doi: 10.1186/s12861-019-0198-4.

Abstract

BACKGROUND

Sonic hedgehog (Shh) is an important signalling protein involved in the induction of early cartilaginous differentiation. Herein, we demonstrate that Shh markedly induces chondrogenesis of rabbit bone marrow stromal cells (BMSCs) under microgravity conditions, and promotes cartilage regeneration.

RESULTS

In the rotary cell culture system (RCCS), chondrogenic differentiation was revealed by stronger Toluidine Blue and collagen II immunohistochemical staining in the Shh transfection group, and chondroinductive activity of Shh was equivalent to that of TGF-β. Western blotting and qRT-PCR analysis results verified the stronger expression of Sox9, aggrecan (ACAN), and collagen II in rabbit BMSCs treated with Shh or TGF-β in a microgravity environment. Low levels of chondrogenic hypertrophy, osteogenesis, and adipogenesis-related factors were detected in all groups. After transplantation in vivo, histological analysis revealed a significant improvement in cartilage and subchondral repair in the Shh transfection group.

CONCLUSIONS

These results suggested that Shh signalling promoted chondrogenesis in rabbit BMSCs under microgravity conditions equivalent to TGF-β, and improved the early stages of the repair of cartilage and subchondral defects. Furthermore, RCCS provided a dynamic culture microenvironment conducive for cell proliferation, aggregation and differentiation.

摘要

背景

音猬因子(Shh)是一种重要的信号蛋白,参与早期软骨分化的诱导。在此,我们证明Shh在微重力条件下能显著诱导兔骨髓间充质干细胞(BMSCs)的软骨形成,并促进软骨再生。

结果

在旋转细胞培养系统(RCCS)中,Shh转染组甲苯胺蓝染色和胶原蛋白II免疫组化染色更强,显示出软骨分化,且Shh的软骨诱导活性与转化生长因子-β(TGF-β)相当。蛋白质免疫印迹和定量逆转录-聚合酶链反应(qRT-PCR)分析结果证实,在微重力环境下用Shh或TGF-β处理的兔BMSCs中,Sox9、聚集蛋白聚糖(ACAN)和胶原蛋白II的表达更强。所有组中检测到的软骨形成肥大、成骨和脂肪生成相关因子水平较低。体内移植后,组织学分析显示Shh转染组软骨和软骨下修复有显著改善。

结论

这些结果表明,在微重力条件下,Shh信号通路促进兔BMSCs的软骨形成,其作用与TGF-β相当,并改善软骨和软骨下缺损修复的早期阶段。此外,RCCS提供了一个有利于细胞增殖、聚集和分化的动态培养微环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8526/6689882/62c72bec0619/12861_2019_198_Fig1_HTML.jpg

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