Suppr超能文献

人骨髓间充质干细胞成骨和成软骨分化过程中两种胶原受体亚家族(整合素和盘状结构域受体)的表达。

The expression of two collagen receptor subfamilies, integrins and discoidin domains during osteogenic and chondrogenic differentiation of human mesenehymal stem cells.

机构信息

Shenzhen Stomatological Hospital, Southern Medical University, Shenzhen, China.

出版信息

Biomed Mater Eng. 2021;32(4):195-205. doi: 10.3233/BME-201151.

Abstract

BACKGROUND

Collagen receptors are characterized by binding to and being activated by collagens. We know little about the molecular mechanism by which the integrins and discoidin domains (DDRs) recognize collagen.

OBJECTIVE

The aim of this study was to investigate the expression of two main collagen receptor subfamilies, integrins and DDRs, during osteogenic and chondrogenic differentiation of human mesenehymal stem cells (hMSCs).

METHODS

Using qRT-PCR, Western blots and FACS, the levels of DDR1, DDR2, integrin subunits β1, α1, α2, α10 and α11 receptors on hMSCs, were assessed upon activation by collagen type I, as well as during osteogenic and chondrogenic differentiation.

RESULTS

The expression of DDR2 and integrin α11β1 was altered compared with other receptors when the cells were cultured under undifferentiated conditions. During osteogenic and chondrogenetic differentiation, DDR2 and α11 were up-regulated during early stages (6 day) of osteogenesis and chondrogenesis, respectively. The expression and activation of DDR2 was concomitant with another receptor integrin subunit β1 during osteogenetic differentiation.

CONCLUSIONS

The results suggested that DDR2 was more specific for osteogenesis than chondrogenesis, while integrin α11β1 was more specific in chondrogenesis. DDR2 and α11 may play a role in the regulation of osteogenesis and chondrogenesis based on the differential expression of these receptors during lineage-dependent changes.

摘要

背景

胶原受体的特征是与胶原结合并被其激活。我们对整联蛋白和盘状结构域(DDR)识别胶原的分子机制知之甚少。

目的

本研究旨在探讨两种主要胶原受体亚家族——整联蛋白和 DDR 在人间充质干细胞(hMSC)成骨和成软骨分化过程中的表达。

方法

通过 qRT-PCR、Western blot 和 FACS,评估 hMSC 对胶原 I 激活以及成骨和成软骨分化过程中 DDR1、DDR2、整合素亚基β1、α1、α2、α10 和α11 受体的表达水平。

结果

与其他受体相比,在未分化条件下培养时,DDR2 和整合素α11β1 的表达发生改变。在成骨和成软骨分化过程中,DDR2 和α11 在成骨和软骨形成的早期(6 天)上调。DDR2 的表达和激活与成骨分化过程中另一个整合素亚基β1 同时发生。

结论

结果表明,DDR2 比软骨生成更特异于成骨,而整合素α11β1 更特异于软骨生成。DDR2 和α11 可能在基于这些受体在谱系依赖性变化过程中的差异表达来调节成骨和软骨生成中发挥作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验