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钙黏蛋白 11 通过 PDGFRβ-ERK1/2 信号通路调节人骨髓间充质干细胞的增殖。

Cadherin-11 Regulates Cell Proliferation via the PDGFRβ-ERK1/2 Signaling Pathway in Human Mesenchymal Stem Cells.

机构信息

MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.

出版信息

Stem Cells. 2022 Mar 16;40(2):165-174. doi: 10.1093/stmcls/sxab019.

Abstract

Controlling stem cell fate is the cornerstone of regenerative medicine. Cadherins have an important role in cell fate commitment and the function of cadherin-11 in the regulation of differentiation in human mesenchymal stem cells (hMSCs) has recently come to light. To better understand how cadherin-11 regulates hMSC behavior, we explored its interaction with receptor tyrosine kinases (RTK), an important family of proteins involved in a myriad of cellular functions. In this study, we provide evidence that cadherin-11, a cell adhesion protein expressed in hMSCs, regulates the activity of several RTKs, including PDGFRβ and PDGFRα. By knocking down cadherin-11 we found that the changes in the RTK activity caused hyperactivation of the MAPK pathways, which were sustained through the phosphorylation and nuclear translocation of ERK1/2 and subsequently caused a decrease in cell proliferation. Together these results provide compelling evidence for the important role of the interaction of cadherin-11 and RTKs in the behavior of hMSCs.

摘要

控制干细胞命运是再生医学的基石。钙黏蛋白在细胞命运决定中起着重要作用,钙黏蛋白-11 在调节人间充质干细胞(hMSCs)分化中的作用最近引起了关注。为了更好地了解钙黏蛋白-11 如何调节 hMSC 的行为,我们探索了它与受体酪氨酸激酶(RTK)的相互作用,RTK 是一个参与多种细胞功能的重要蛋白质家族。在这项研究中,我们提供了证据表明,在 hMSCs 中表达的细胞黏附蛋白钙黏蛋白-11 调节几种 RTK 的活性,包括 PDGFRβ 和 PDGFRα。通过敲低钙黏蛋白-11,我们发现 RTK 活性的变化导致 MAPK 途径的过度激活,这通过 ERK1/2 的磷酸化和核转位得到维持,随后导致细胞增殖减少。这些结果为钙黏蛋白-11 和 RTKs 相互作用在 hMSCs 行为中的重要作用提供了有力的证据。

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