Endolysosomal proteolysis and its regulation

被引:261
作者
Pillay, CS [1 ]
Elliott, E [1 ]
Dennison, C [1 ]
机构
[1] Univ KwaZulu Natal, Sch Mol & Cellular Biosci, ZA-3209 Pietermaritzburg, South Africa
关键词
autophagy; endosome; lysosome; proteolysis;
D O I
10.1042/0264-6021:3630417
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
The endolysosomal system comprises a unique environment for proteolysis, which is regulated in a manner that apparently does not involve protease inhibitors. The system comprises a series of membrane-bound intracellular compartments, within which endocytosed material and redundant cellular components are hydrolysed. Endocytosed material tends to flow vectorially through the system, proceeding through the early endosome, the endosome carrier vesicle, the late endosome and the lysosome, Phagocytosis and autophagy provide alternative entry points into the system. Late endosomes, lysosome/late endosome hybrid organelles, phagosomes and autophagosomes are the principal sites for proteolysis. In each case. hydrolytic competence is due to components of the endolysosomal system, i.e. proteases, lysosome-associated membrane proteins, H+-ATPases and possibly cysteine transporters. The view is emerging that lysosomes are organelles for the storage of hydrolases, perhaps in an inactivated form. Once a substrate has entered a proteolytically competent environment. the rate-limiting proteoilytic steps are probably effected by cysteine endoproteinases. As these are affected by pH and possibly redox potential, they may be regulated by the organelle luminal environment. Regulation is probably also affected, among other factors, by organelle fusion reactions. whereby the meeting of enzyme and substrate may be controlled. Such systems would permit simultaneous regulation of a number of unrelated hydrolases.
引用
收藏
页码:417 / 429
页数:13
相关论文
共 146 条
[1]   Normal lysosomal morphology and function in LAMP-1-deficient mice [J].
Andrejewski, N ;
Punnonen, EL ;
Guhde, G ;
Tanaka, Y ;
Lüllmann-Rauch, R ;
Hartmann, D ;
von Figura, K ;
Saftig, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (18) :12692-12701
[2]   Regulated secretion of conventional lysosomes [J].
Andrews, NW .
TRENDS IN CELL BIOLOGY, 2000, 10 (08) :316-321
[3]   CYTOPLASMIC DYNEIN-DEPENDENT VESICULAR TRANSPORT FROM EARLY TO LATE ENDOSOMES [J].
ANIENTO, F ;
EMANS, N ;
GRIFFITHS, G ;
GRUENBERG, J .
JOURNAL OF CELL BIOLOGY, 1993, 123 (06) :1373-1387
[4]   Enzymatic reduction of disulfide bonds in lysosomes: Characterization of a Gamma-interferon-inducible lysosomal thiol reductase (GILT) [J].
Arunachalam, B ;
Phan, UT ;
Geuze, HJ ;
Cresswell, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (02) :745-750
[5]  
Bakker AC, 1997, J CELL SCI, V110, P2227
[6]   PHYSIOLOGICAL FUNCTIONS OF ENDOSOMAL PROTEOLYSIS [J].
BERG, T ;
GJOEN, T ;
BAKKE, O .
BIOCHEMICAL JOURNAL, 1995, 307 :313-326
[7]   Autophagic proteolysis: Control and specificity [J].
Blommaart, EFC ;
Luiken, JJFP ;
Meijer, AJ .
HISTOCHEMICAL JOURNAL, 1997, 29 (05) :365-385
[8]   PROTEASES AND PROTEOLYSIS IN THE LYSOSOME [J].
BOHLEY, P ;
SEGLEN, PO .
EXPERIENTIA, 1992, 48 (02) :151-157
[9]  
Bright NA, 1997, J CELL SCI, V110, P2027
[10]  
BROMME D, 1998, HDB PROTEOLYTIC ENZY, P624