磷酸化
肌球蛋白轻链激酶
血管生成
肌球蛋白
细胞生物学
免疫球蛋白轻链
化学
癌症研究
生物
免疫学
抗体
作者
Kiyomi Tsuji‐Tamura,Mari Sato,Masato Tamura
标识
DOI:10.1016/j.cellsig.2024.111223
摘要
Control of angiogenesis is widely considered a therapeutic strategy, but reliable control methods are still under development. Phosphorylation of myosin light chain 2 (MLC2), which regulates actin-myosin interaction, is critical to the behavior of vascular endothelial cells (ECs) during angiogenesis. MLC2 is phosphorylated by MLC kinase (MLCK) and dephosphorylated by MLC phosphatase (MLCP) containing a catalytic subunit PP1. We investigated the potential role of MLC2 in the pharmacological control of angiogenesis.
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