Regulating cell migration: calpains make the cut

被引:388
作者
Franco, SJ
Huttenlocher, A [1 ]
机构
[1] Univ Wisconsin, Dept Pediat, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Pharmacol, Madison, WI 53705 USA
[3] Univ Wisconsin, Mol & Cellular Biol Program, Madison, WI 53705 USA
关键词
calpain; cell motility; proteolysis;
D O I
10.1242/jcs.02562
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The calpain family of proteases has been implicated in cellular processes such as apoptosis, proliferation and cell migration. Calpains are involved in several key aspects of migration, including: adhesion and spreading; detachment of the rear; integrin- and growth-factor-mediated signaling; and membrane protrusion. Our understanding of how calpains are activated and regulated during cell migration has increased as studies have identified roles for calcium and phospholipid binding, autolysis, phosphorylation and inhibition by calpastatin in the modulation of calpain activity. Knockout and knockdown approaches have also contributed significantly to our knowledge of calpain biology, particularly with respect to the specific functions of different calpain isoforms. The mechanisms by which calpain-mediated proteolysis of individual substrates contributes to cell motility have begun to be addressed, and these efforts have revealed roles for proteolysis of specific substrates in integrin activation, adhesion complex turnover and membrane protrusion dynamics. Understanding these mechanisms should provide avenues for novel therapeutic strategies to treat pathological processes such as tumor metastasis and chronic inflammatory disease.
引用
收藏
页码:3829 / 3838
页数:10
相关论文
共 146 条
[1]   Disruption of the murine calpain small subunit gene, Capn4:: Calpain is essential for embryonic development but not for cell growth and division [J].
Arthur, JSC ;
Elce, JS ;
Hegadorn, C ;
Williams, K ;
Greer, PA .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (12) :4474-4481
[2]   Investigation of the interaction of m-calpain with phospholipids: Calpain-phospholipid interactions [J].
Arthur, JSC ;
Crawford, C .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1996, 1293 (02) :201-206
[3]   Disruption of the mouse μ-calpain gene reveals an essential role in platelet function [J].
Azam, M ;
Andrabi, SS ;
Sahr, KE ;
Kamath, L ;
Kuliopulos, A ;
Chishti, AH .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (06) :2213-2220
[4]   Autolysis parallels activation of mu-calpain [J].
Baki, A ;
Tompa, P ;
Alexa, A ;
Molnar, O ;
Friedrich, P .
BIOCHEMICAL JOURNAL, 1996, 318 :897-901
[5]  
Barnoy S, 1999, J CELL BIOCHEM, V74, P522, DOI 10.1002/(SICI)1097-4644(19990915)74:4<522::AID-JCB2>3.0.CO
[6]  
2-I
[7]   COLOCALIZATION OF CALCIUM-DEPENDENT PROTEASE-II AND ONE OF ITS SUBSTRATES AT SITES OF CELL-ADHESION [J].
BECKERLE, MC ;
BURRIDGE, K ;
DEMARTINO, GN ;
CROALL, DE .
CELL, 1987, 51 (04) :569-577
[8]  
Bhatt A, 2002, J CELL SCI, V115, P3415
[9]   Evidence that β3 integrin-induced Rac activation involves the calpain-dependent formation of integrin clusters that are distinct from the focal complexes and focal adhesions that form as Rac and RhoA become active [J].
Bialkowska, K ;
Kulkarni, S ;
Du, XP ;
Goll, DE ;
Saido, TC ;
Fox, JEB .
JOURNAL OF CELL BIOLOGY, 2000, 151 (03) :685-695
[10]   SH3 domain of spectrin participates in the. activation of Rac in specialized calpain-induced integrin signaling complexes [J].
Bialkowska, K ;
Saido, TC ;
Fox, JEB .
JOURNAL OF CELL SCIENCE, 2005, 118 (02) :381-395