Integrity of the cortical actin ring is required for activation of the PI3K/Akt and p38 MAPK signaling pathways in redifferentiation of chondrocytes on chitosan

被引:29
作者
Park, Eun Hee [1 ]
Kang, Shin-Sung [1 ]
Lee, Young-Sup [2 ]
Kim, Song-Ja [3 ]
Jin, Eun-Jung [4 ]
Tak, Eun Nam [1 ]
Sonn, Jong Kyung [1 ]
机构
[1] Kyungpook Natl Univ, Coll Nat Sci, Dept Biol, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Coll Nat Sci, Dept Biochem, Taegu, South Korea
[3] Kongju Natl Univ, Coll Nat Sci, Dept Life Sci, Kong Ju 314701, South Korea
[4] Wonkwang Univ, Coll Nat Sci, Div Biol Sci, Iksan, South Korea
关键词
Chondrogenesis; Redifferentiation; Citosan; Cytoskeleton; Akt; p38; MAPK;
D O I
10.1016/j.cellbi.2008.07.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell shape alterations and accompanying cytoskeletal changes have diverse effects on cell function. We have already shown that dedifferentiated chondrocytes have a round cell morphology and undergo redifferentiation when cultured on chitosan membrane. In the present study, we investigate the role of the cytoskeleton in chondrocyte redifferentiation. Chondrocytes obtained from a micromass culture of chick limb bud mesenchymal cells were subcultured four times. Immunofluorescence analysis of F-actin showed cortical distribution of the actin cytoskeleton upon subculture of dedifferentiated chondrocytes on chitosan membrane. Treatment with cytochalasin D disrupted the cortical actin ring formed during cultivation of chondrocytes on the chitosan membrane, and inhibited chondrocyte redifferentiation. Moreover, cytochalasin D inhibited the phosphorylation of Akt and p38 mitogen activated protein kinase (MAPK), induced during redifferentiation on chitosan membrane. LY294002, an inhibitor of phosphatidylinositol-3-OH-kinase (PI3K), suppressed chondrocyte redifferentiation. These findings suggest that integrity of the actin cytoskeleton is a crucial requirement for PI3K/Akt and p38 MAPK in chondrocyte redifferentiation. (c) 2008 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1272 / 1278
页数:7
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