MEKK1 regulates calpain-dependent proteolysis of focal adhesion proteins for rear-end detachment of migrating fibroblasts

被引:104
作者
Cuevas, BD [1 ]
Abell, AN
Witowsky, JA
Yujiri, T
Johnson, NL
Kesavan, K
Ware, M
Jones, PL
Weed, SA
DeBiasi, RL
Oka, Y
Tyler, KL
Johnson, GL
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Pharmacol, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Pediat, Denver, CO 80262 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Neurol, Denver, CO 80262 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80262 USA
[5] Univ Colorado, Hlth Sci Ctr, Dept Cell & Struct Biol, Denver, CO 80262 USA
[6] Univ Colorado, Hlth Sci Ctr, Dept Craniofacial Biol, Denver, CO 80262 USA
[7] Denver Vet Affairs Med Ctr, Denver, CO 80220 USA
[8] Yamaguchi Univ Med, Dept Internal Med 3, Yamaguchi, Japan
关键词
calpain; MEKK1; rear-end detachment;
D O I
10.1093/emboj/cdg322
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Herein, we define how MEKK1, a MAPK kinase kinase, regulates cell migration. MEKK1 is associated with actin fibers and focal adhesions, localizing MEKK1 to sites critical in the control of cell adhesion and migration. EGF-induced ERK1/2 activation and chemotaxis are inhibited in MEKK1-/- fibroblasts. MEKK1 deficiency causes loss of vinculin in focal adhesions of migrating cells, increased cell adhesion and impeded rear-end detachment. MEKK1 is required for activation of the cysteine protease calpain and cleavage of spectrin and talin, proteins linking focal adhesions to the cytoskeleton. Inhibition of ERK1/2 or calpain, but not of JNK, mimics MEKK1 deficiency. Therefore, MEKK1 regulates calpain-mediated substratum release of migrating fibroblasts.
引用
收藏
页码:3346 / 3355
页数:10
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