Damage control: cellular mechanisms of plasma membrane repair

被引:227
作者
Andrews, Norma W. [1 ]
Almeida, Patricia E. [1 ,2 ]
Corrotte, Matthias [1 ]
机构
[1] Univ Maryland, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA
[2] Univ Fed Juiz de Fora, Dept Biol, Juiz De Fora, MG, Brazil
基金
美国国家卫生研究院;
关键词
injury; resealing; endocytosis; caveolae; muscular dystrophy; INDEPENDENT ENDOCYTOSIS; ACID SPHINGOMYELINASE; REGULATED SECRETION; STREPTOLYSIN-O; EXOCYTOSIS; LYSOSOMES; CELLS; CALCIUM; INJURY; VESICLES;
D O I
10.1016/j.tcb.2014.07.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
When wounded, eukaryotic cells reseal in a few seconds. Ca2+ influx induces exocytosis of lysosomes, a process previously thought to promote repair by 'patching' wounds. New evidence suggests that resealing involves direct wound removal. Exocytosis of lysosomal acid sphingomyelinase (ASM) triggers endocytosis of lesions followed by intracellular degradation. Characterization of injury-induced endosomes revealed a role for caveolae, sphingolipid-enriched plasma membrane invaginations that internalize toxin pores and are abundant in mechanically stressed cells. These findings provide a novel mechanistic explanation for the muscle pathology associated with mutations in caveolar proteins. Membrane remodeling by the ESCRT complex was also recently shown to participate in small-wound repair, emphasizing that cell resealing involves previously unrecognized mechanisms for lesion removal that are distinct from the patch model.
引用
收藏
页码:734 / 742
页数:9
相关论文
共 40 条
[21]   Perforin triggers a plasma membrane-repair response that facilitates CTL induction of apoptosis [J].
Keefe, D ;
Shi, LF ;
Feske, S ;
Massol, R ;
Navarro, F ;
Kirchhausen, T ;
Lieberman, J .
IMMUNITY, 2005, 23 (03) :249-262
[22]   Streptolysin O clearance through sequestration into blebs that bud passively from the plasma membrane [J].
Keyel, Peter A. ;
Loultcheva, Lyussiena ;
Roth, Robyn ;
Salter, Russell D. ;
Watkins, Simon C. ;
Yokoyama, Wayne M. ;
Heuser, John E. .
JOURNAL OF CELL SCIENCE, 2011, 124 (14) :2414-2423
[23]   Massive calcium-activated endocytosis without involvement of classical endocytic proteins [J].
Lariccia, Vincenzo ;
Fine, Michael ;
Magi, Simona ;
Lin, Mei-Jung ;
Yaradanakul, Alp ;
Llaguno, Marc C. ;
Hilgemann, Donald W. .
JOURNAL OF GENERAL PHYSIOLOGY, 2011, 137 (01) :111-132
[24]   Dysferlin interacts with Annexins A1 and A2 and mediates sarcolemmal wound-healing [J].
Lennon, NJ ;
Kho, A ;
Bacskai, BJ ;
Perlmutter, SL ;
Hyman, BT ;
Brown, RH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (50) :50466-50473
[25]   RAB-5-and RAB-11-Dependent Vesicle-Trafficking Pathways Are Required for Plasma Membrane Repair after Attack by Bacterial Pore-Forming Toxin [J].
Los, Ferdinand C. O. ;
Kao, Cheng-Yuan ;
Smitham, Jane ;
McDonald, Kent L. ;
Ha, Christine ;
Peixoto, Christina A. ;
Aroian, Raffi V. .
CELL HOST & MICROBE, 2011, 9 (02) :147-157
[26]  
McNeil PL, 2000, J CELL SCI, V113, P1891
[27]   An emergency response team for membrane repair [J].
McNeil, PL ;
Kirchhausen, T .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (06) :499-505
[28]   Vesicle accumulation and exocytosis at sites of plasma membrane disruption [J].
Miyake, K ;
McNeil, PL .
JOURNAL OF CELL BIOLOGY, 1995, 131 (06) :1737-1745
[29]   THE RECOVERY OF HUMAN POLYMORPHONUCLEAR LEUKOCYTES FROM SUBLYTIC COMPLEMENT ATTACK IS MEDIATED BY CHANGES IN INTRACELLULAR FREE CALCIUM [J].
MORGAN, BP ;
CAMPBELL, AK .
BIOCHEMICAL JOURNAL, 1985, 231 (01) :205-208
[30]   Formation and release of arrestin domain-containing protein 1-mediated microvesicles (ARMMs) at plasma membrane by recruitment of TSG101 protein [J].
Nabhan, Joseph F. ;
Hu, Ruoxi ;
Oh, Raymond S. ;
Cohen, Stanley N. ;
Lu, Quan .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (11) :4146-4151