Rho-ROCK signal pathway regulates microtubule-based process formation of cultured podocytes - Inhibition of ROCK promoted process elongation

被引:42
作者
Gao, SY
Li, CY
Chen, J
Pan, L
Saito, S
Terashita, T
Saito, K
Miyawaki, K
Shigemoto, K
Mominoki, K
Matsuda, S
Kobayashi, N [1 ]
机构
[1] Ehime Univ, Sch Med, Dept Anat & Embryol, Shigenobu, Ehime 7910295, Japan
[2] Ehime Univ, Sch Med, Dept Hyg, Shigenobu, Ehime 7910295, Japan
[3] Ehime Univ, Integrated Ctr Sci, Dept Biol Resources, Shigenobu, Ehime 7910295, Japan
来源
NEPHRON EXPERIMENTAL NEPHROLOGY | 2004年 / 97卷 / 02期
关键词
renal glomerulus; podocyte; process formation; cytoskeleton; microtubule; Rho; ROCK; Y-27632;
D O I
10.1159/000078406
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: 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. Method: 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. Results: Inhibition of ROCK significantly enhanced the formation of thick processes containing MT bundles. Y27632 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. Conclusions: 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. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:E49 / E61
页数:13
相关论文
共 38 条
[1]  
Kriz W., Kobayashi N., Elger M., New aspects of podocyte structure, function and pathology, Clin Exp Nephrol, 2, pp. 85-99, (1998)
[2]  
Pavenstadt H., Kriz W., Kretzler M., Cell biology of the glomerular podocyte, Physiol Rev, 83, pp. 253-307, (2003)
[3]  
Mundel P., Shankland S.J., Podocyte biology and response to injury, J Am Soc Nephrol, 13, pp. 3005-3015, (2002)
[4]  
Kreidberg J.A., Podocyte differentiation and glomerulogenesis, J Am Soc Nephrol, 14, pp. 806-814, (2003)
[5]  
Kobayashi N., Mundel P., A role of microtubules during the formation of cell processes in neuronal and non-neuronal cells, Cell Tissue Res, 291, pp. 163-174, (1998)
[6]  
Kobayashi N., Mechanism of the process formation: Podocytes versus neurons, Microsc Res Tech, 57, pp. 217-223, (2002)
[7]  
Ichimura K., Kurihara H., Sakai T., Actin filament organization of foot processes in rat podocytes, J Histochem Cytochem, 51, pp. 1589-1600, (2003)
[8]  
Mundel P., Reiser J., Zuniga Mejia Borja A., Pavenstadt H., Davidson G.R., Kriz W., Zeller R., Rearrangements of the cytoskeleton and cell contacts induce process formation during differentiation of conditionally immortalized mouse podocyte cell lines, Exp Cell Res, 236, pp. 248-258, (1997)
[9]  
Kobayashi N., Reiser J., Kriz W., Kuriyama R., Mundel P., Nonuniform microtubular polarity established by CHO1/MKLP1 motor protein is necessary for process formation of podocytes, J Cell Biol, 143, pp. 1961-1970, (1998)
[10]  
Kobayashi N., Mominoki K., Wakisaka H., Shimazaki Y., Matsuda S., Morphogenetic activity of extracellular matrices on cultured podocytes. Laminin accelerates podocyte process formation in vitro, Ital J Anat Embryol, 106, 1 SUPPL., pp. 423-430, (2001)