Gao Shuang-Yan, Li Chun-Yu, Chen Jie, Pan Lei, Saito Shouichiro, Terashita Takehiro, Saito Kyoko, Miyawaki Kyojy, Shigemoto Kazuhiro, Mominoki Katsumi, Matsuda Seiji, Kobayashi Naoto
Department of Anatomy and Embryology, Integrated Center for Science, Ehime University, Ehime, Japan.
Nephron Exp Nephrol. 2004;97(2):e49-61. doi: 10.1159/000078406.
Podocytes, renal glomerular visceral epithelial cells, have two kinds of processes, namely major processes containing microtubules (MTs) and foot processes with actin filaments (AFs). The present study investigated how MTs are organized by the Rho-ROCK signal transduction pathway during process formation of podocytes.
After induction of differentiation, podocytes of the conditionally immortalized mouse cell line were treated with Y-27632, a specific inhibitor of ROCK, and exoenzyme C3, an inhibitor of RhoA, as well as with forskolin whose effects include inhibition of RhoA, in order to inhibit the Rho-ROCK pathway.
Inhibition of ROCK significantly enhanced the formation of thick processes containing MT bundles. Y-27632 promoted process formation even in the presence of latrunculin A which disrupts AFs, strongly suggesting that ROCK directly regulates MT assembly. Treatment with Y-27632 increased MT stability, and stabilized MTs preferentially localized in podocyte processes. Moreover, when treated with a combination of Y-27632 and forskolin, and with Y-27632 and C3 as well, podocytes developed not only MT-based thick processes but also AF-based thin projections.
These data indicate a contribution of ROCK in MT organization to promote podocyte process formation, although it was originally thought to regulate AF assembly. AF-based thin projections seem to be induced mainly by inhibition of RhoA and ROCK. The present study reveals a significant role of the Rho-ROCK signal pathway in the reorganization of both MTs and AFs during process formation of podocytes.
足细胞,即肾小肾小球脏层上皮细胞,有两种突起,即含有微管(MTs)的主突起和含有肌动蛋白丝(AFs)的足突。本研究调查了在足细胞突起形成过程中,微管如何通过Rho-ROCK信号转导途径进行组织。
在诱导分化后,用ROCK的特异性抑制剂Y-27632、RhoA的抑制剂外切酶C3以及作用包括抑制RhoA的福斯可林处理条件性永生化小鼠细胞系的足细胞,以抑制Rho-ROCK途径。
抑制ROCK显著增强了含有微管束的粗突起的形成。即使在存在破坏肌动蛋白丝的拉春库林A的情况下,Y-27632仍能促进突起形成,这强烈表明ROCK直接调节微管组装。用Y-27632处理可增加微管稳定性,且优先定位于足细胞突起中的微管更稳定。此外,当用Y-27632与福斯可林的组合以及Y-27632与C3的组合处理时,足细胞不仅形成了基于微管的粗突起,还形成了基于肌动蛋白丝的细突起。
这些数据表明,尽管最初认为ROCK调节肌动蛋白丝组装,但ROCK在微管组织中对促进足细胞突起形成有作用。基于肌动蛋白丝的细突起似乎主要由RhoA和ROCK的抑制诱导。本研究揭示了Rho-ROCK信号通路在足细胞突起形成过程中对微管和肌动蛋白丝重组的重要作用。