Periodic mechanical stress enhances rat chondrocyte area expansion and migration through Src-PLCγ1-ERK1/2 signaling

被引:37
作者
Nong, Luming [1 ]
Yin, Guoyong [1 ]
Ren, Kewei [1 ]
Tang, Jilei [1 ]
Fan, Weimin [1 ]
机构
[1] Nanjing Med Univ, Dept Orthoped, Affiliated Hosp 1, Nanjing 210029, Peoples R China
关键词
Periodic mechanical stress; Chondrocyte area expansion and migration; Src; PLC gamma 1; ERK1/2; PHOSPHOLIPASE C-GAMMA; EXTRACELLULAR-MATRIX; ARTICULAR-CARTILAGE; ACTIVATION; KINASE; SRC; STIMULATION; GIT1;
D O I
10.1016/j.ejcb.2010.04.005
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The signal transduction pathways of chondrocyte area expansion and migration under periodic mechanical stress remain a matter of debate. We explore this question by performing cell culture experiments in our self-developed periodic stress field and perfusion culture system. Under periodic mechanical stress, we find that both rat chondrocyte area and migration are significantly amplified. These changes are associated with increases in the phosphorylation of Src, PLC gamma 1 and ERK1/2. Area expansion, migration and phosphorylation of PLC gamma 1-Tyr(783) and ERK1/2-Thr(202)/Tyr(204) are inhibited (p < 0.05) after pretreatment with Src inhibitor (PP2). We further demonstrate that area expansion, migration and phosphorylation of ERK1/2-Thr(202)/Tyr(204) are significantly inhibited (p < 0.05) after pretreatment with PLC gamma 1 inhibitor (U73122); the phosphorylation site of Src-Tyr(418) is not affected. After pretreatment with an ERK1/2 inhibitor (PD98059), area expansion and migration are inhibited (p < 0.05), while the phosphorylation sites of Src-Tyr(418) and PLC gamma 1-Tyr(783) are not affected. These findings suggest that periodic mechanical stress promotes chondrocyte area expansion and migration in part through the Src-PLC gamma 1-ERK1/2 signaling pathway. (C) 2010 Elsevier GmbH. All rights reserved.
引用
收藏
页码:705 / 711
页数:7
相关论文
共 25 条
[1]
A bit of give and take: the relationship between the extracellular matrix and the developing chondrocyte [J].
Behonick, DJ ;
Werb, Z .
MECHANISMS OF DEVELOPMENT, 2003, 120 (11) :1327-1336
[2]
Phospholipase C-γ as a signal-transducing element [J].
Carpenter, G ;
Ji, QS .
EXPERIMENTAL CELL RESEARCH, 1999, 253 (01) :15-24
[3]
Repetitive deformation activates focal adhesion kinase and ERK mitogenic signals in human caco-2 intestinal epithelial cells through Src and Rac1 [J].
Chaturvedi, Lakshmi S. ;
Marsh, H. Michael ;
Shang, Xun ;
Zheng, Yi ;
Basscon, Marc D. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (01) :14-28
[4]
Cyclic compressive mechanical stimulation induces sequential catabolic and anabolic gene changes in chondrocytes resulting in increased extracellular matrix accumulation [J].
De Croos, J. N. A. ;
Dhaliwal, S. S. ;
Grynpas, M. D. ;
Pilliar, R. M. ;
Kandel, R. A. .
MATRIX BIOLOGY, 2006, 25 (06) :323-331
[5]
GIT1 mediates Src-dependent activation of phospholipase Cγ by angiotensin II and epidermal growth factor [J].
Haendeler, J ;
Yin, GY ;
Hojo, Y ;
Saito, Y ;
Melaragno, M ;
Yan, C ;
Sharma, VK ;
Heller, M ;
Aebersold, R ;
Berk, BC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (50) :49936-49944
[6]
TRANSCRIPTIONAL REGULATION BY EXTRACELLULAR SIGNALS - MECHANISMS AND SPECIFICITY [J].
HILL, CS ;
TREISMAN, R .
CELL, 1995, 80 (02) :199-211
[7]
Integrins: Bidirectional, allosteric signaling machines [J].
Hynes, RO .
CELL, 2002, 110 (06) :673-687
[8]
Serotonin stimulates GnRH secretion through the c-Src-PLC γ1 pathway in GT1-7 hypothalamic cells [J].
Kim, Hyeon Soo ;
Yumkham, Sanatombi ;
Choi, Jang Hyun ;
Son, Gi Hoon ;
Kim, Kyungjin ;
Ryu, Sung Ho ;
Suh, Pann-Ghill .
JOURNAL OF ENDOCRINOLOGY, 2006, 190 (03) :581-591
[9]
Microenvironment regulation of extracellular signal-regulated kinase activity in chondrocytes - Effects of culture configuration, interleukin-1, and compressive stress [J].
Li, KW ;
Wang, AS ;
Sah, RL .
ARTHRITIS AND RHEUMATISM, 2003, 48 (03) :689-699
[10]
An in vitro analysis of mechanical wounding-induced ligand-independent KGFR activation [J].
Li, Min ;
Firth, James D. ;
Putnins, Edward E. .
JOURNAL OF DERMATOLOGICAL SCIENCE, 2009, 53 (03) :182-191