Key Laboratory for Biomechanics and Mechanobiology of Ministry of Education, School of Biological Science and Medical Engineering, Beihang University, Beijing, China.
Beijing Advanced Innovation Centre for Biomedical Engineering, Beihang University, Beijing, China.
J Cell Mol Med. 2020 Mar;24(6):3739-3744. doi: 10.1111/jcmm.15014. Epub 2020 Feb 17.
Mechanical stimulation is an important factor regulating mesenchymal stem cell (MSC) functions such as proliferation. The Ca -activated K channel, K 3.1, is critically engaged in MSC proliferation but its role in mechanical regulation of MSC proliferation remains unknown. Here, we examined the K 3.1 channel expression and its role in rat bone marrow-derived MSC (BMSC) proliferation in response to mechanical stretch. Application of mechanical stretch stimulated BMSC proliferation via promoting cell cycle progression. Such mechanical stimulation up-regulated the K 3.1 channel expression and pharmacological or genetic inhibition of the K 3.1 channel strongly suppressed stretch-induced increase in cell proliferation and cell cycle progression. These results support that the K 3.1 channel plays an important role in transducing mechanical forces to MSC proliferation. Our finding provides new mechanistic insights into how mechanical stimuli regulate MSC proliferation and also a viable bioengineering approach to improve MSC proliferation.
机械刺激是调节间充质干细胞(MSC)功能的重要因素,如增殖。钙激活的钾通道,K3.1,在 MSC 增殖中起着关键作用,但它在机械调节 MSC 增殖中的作用尚不清楚。在这里,我们研究了 K3.1 通道的表达及其在机械拉伸刺激大鼠骨髓来源的间充质干细胞(BMSC)增殖中的作用。机械拉伸刺激 BMSC 增殖,促进细胞周期进程。这种机械刺激上调 K3.1 通道的表达,药理学或遗传学抑制 K3.1 通道强烈抑制拉伸诱导的细胞增殖和细胞周期进程增加。这些结果表明 K3.1 通道在将机械力转导为 MSC 增殖中起着重要作用。我们的发现为机械刺激如何调节 MSC 增殖提供了新的机制见解,也为改善 MSC 增殖提供了一种可行的生物工程方法。