Song Min Seok, Choi Seon Young, Ryu Pan Dong, Lee So Yeong
Laboratory of Veterinary Pharmacology, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, Seoul, Korea.
PLoS One. 2016 Feb 5;11(2):e0148633. doi: 10.1371/journal.pone.0148633. eCollection 2016.
Voltage-gated K+ (Kv) channels are well known to be involved in cell proliferation. However, even though cell proliferation is closely related to cell differentiation, the relationship between Kv channels and cell differentiation remains poorly investigated. This study demonstrates that Kv3.3 is involved in K562 cell erythroid differentiation. Down-regulation of Kv3.3 using siRNA-Kv3.3 increased hemin-induced K562 erythroid differentiation through decreased activation of signal molecules such as p38, cAMP response element-binding protein, and c-fos. Down-regulation of Kv3.3 also enhanced cell adhesion by increasing integrin β3 and this effect was amplified when the cells were cultured with fibronectin. The Kv channels, or at least Kv3.3, appear to be associated with cell differentiation; therefore, understanding the mechanisms of Kv channel regulation of cell differentiation would provide important information regarding vital cellular processes.
电压门控钾离子(Kv)通道与细胞增殖密切相关,这一点广为人知。然而,尽管细胞增殖与细胞分化密切相关,但Kv通道与细胞分化之间的关系仍鲜有研究。本研究表明,Kv3.3参与K562细胞的红系分化。使用siRNA-Kv3.3下调Kv3.3可通过降低p38、cAMP反应元件结合蛋白和c-fos等信号分子的激活来增强血红素诱导的K562红系分化。下调Kv3.3还可通过增加整合素β3增强细胞黏附,当细胞与纤连蛋白一起培养时,这种作用会被放大。Kv通道,或者至少是Kv3.3,似乎与细胞分化有关;因此,了解Kv通道调节细胞分化的机制将为重要的细胞过程提供重要信息。