A family of hsp60-related proteins in pancreatic beta cells of non-obese diabetic (NOD) mice

被引:6
作者
Brudzynski, K
Cunningham, IA
Martinez, V
机构
[1] UNIV HOSP,ROBARTS RES INST,IMMUNOL GRP,TORONTO,ON N6A 5K8,CANADA
[2] UNIV HOSP,ROBARTS RES INST,IMAGING RES LAB,TORONTO,ON N6A 5K8,CANADA
[3] UNIV HOSP,DEPT PATHOL,TORONTO,ON N6A 5K8,CANADA
关键词
D O I
10.1016/S0896-8411(95)80022-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Eukaryotic hsp60s are plastid-specific molecular chaperones implicated in the pathogenesis of many inflammatory and autoimmune diseases. We have used immunoelectron microscopy, immunoblotting and subcellular fractionation of islet cells to determine whether analogous proteins with related function are expressed in other cellular structures and whether such hsp60-related proteins could serve as antigenic targets in autoimmune diabetes. Using a panel of monoclonal and polyclonal antibodies to human and yeast hsp60s and immunoelectron microscopy, the hspb0 antibody cross-reactive proteins were detected in secretory granules, mitochondria, synaptic-like microvesicles and microtubules of mouse pancreatic beta cells. The expression of microtubule-associated hsp60 was induced by an infiltration of islets by mononuclear cells. This novel inducible-form of hsp60-related protein was recognized as an antigen by sera from diabetic mice. Subcellular fractionation of islets indicated that the molecular size of hsp60-related proteins included 66, 62, 58, 55, 52 and 38 kDa. These results demonstrate that the pancreatic beta cells express a family of hsp60-related proteins, with members differentially expressed in distinct cellular compartments. These proteins bearing hsp60 epitopes were antigenic targets for autoimmune responses in diabetic NOD mice. (C) 1995 Academic Press Limited
引用
收藏
页码:859 / 874
页数:16
相关论文
共 38 条
[1]
A CHAPERONIN PROTEIN MODULE INVOLVED IN RECOGNITION OF INTERACTIVE PROTEIN SURFACES [J].
ALCONADA, A ;
CUEZVA, JM .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (03) :81-82
[2]
BIRNBAUM G, 1991, ANN NEUROL, V30, P305
[3]
TRANSIENT ASSOCIATION OF NEWLY SYNTHESIZED UNFOLDED PROTEINS WITH THE HEAT-SHOCK GROEL PROTEIN [J].
BOCHKAREVA, ES ;
LISSIN, NM ;
GIRSHOVICH, AS .
NATURE, 1988, 336 (6196) :254-257
[4]
2 MONOCLONAL-ANTIBODIES GENERATED AGAINST HUMAN HSP60 SHOW REACTIVITY WITH SYNOVIAL MEMBRANES OF PATIENTS WITH JUVENILE CHRONIC ARTHRITIS [J].
BOOG, CJP ;
DEGRAEFFMEEDER, ER ;
LUCASSEN, MA ;
VANDERZEE, R ;
VOORHORSTOGINK, MM ;
VANKOOTEN, PJS ;
GEUZE, HJ ;
VANEDEN, W .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (06) :1805-1810
[5]
SECRETORY GRANULE AUTOANTIGEN IN INSULIN-DEPENDENT DIABETES-MELLITUS IS RELATED TO 62 KDA HEAT-SHOCK PROTEIN (HSP60) [J].
BRUDZYNSKI, K ;
MARTINEZ, V ;
GUPTA, RS .
JOURNAL OF AUTOIMMUNITY, 1992, 5 (04) :453-463
[7]
IMMUNOCYTOCHEMICAL LOCALIZATION OF HEAT-SHOCK PROTEIN-60-RELATED PROTEIN IN BETA-CELL SECRETORY GRANULES AND ITS ALTERED DISTRIBUTION IN NONOBESE DIABETIC MICE [J].
BRUDZYNSKI, K ;
MARTINEZ, V ;
GUPTA, RS .
DIABETOLOGIA, 1992, 35 (04) :316-324
[8]
SYNAPTOPHYSIN-CONTAINING MICROVESICLES TRANSPORT HEAT-SHOCK PROTEIN HSP60 IN INSULIN-SECRETING BETA-CELLS [J].
BRUDZYNSKI, K ;
MARTINEZ, V .
CYTOTECHNOLOGY, 1993, 11 (01) :23-33
[9]
MITOCHONDRIAL HEAT-SHOCK PROTEIN HSP60 IS ESSENTIAL FOR ASSEMBLY OF PROTEINS IMPORTED INTO YEAST MITOCHONDRIA [J].
CHENG, MY ;
HARTL, FU ;
MARTIN, J ;
POLLOCK, RA ;
KALOUSEK, F ;
NEUPERT, W ;
HALLBERG, EM ;
HALLBERG, RL ;
HORWICH, AL .
NATURE, 1989, 337 (6208) :620-625
[10]
MOLECULAR CHAPERONES AND THE BIOGENESIS OF MITOCHONDRIA AND PEROXISOMES [J].
CUEZVA, JM ;
FLORES, AI ;
LIRAS, A ;
SANTAREN, JF ;
ALCONADA, A .
BIOLOGY OF THE CELL, 1993, 77 (01) :47-62