Novel immunolocalization of α-synuclein in human muscle of inclusion-body myositis, regenerating and necrotic muscle fibers, and at neuromuscular junctions

被引:85
作者
Askanas, V [1 ]
Engel, WK [1 ]
Alvarez, RB [1 ]
McFerrin, J [1 ]
Broccolini, A [1 ]
机构
[1] Univ So Calif, Neuromuscular Ctr, Dept Neurol, Keck Sch Med,Good Samaritan Hosp, Los Angeles, CA 90017 USA
关键词
alpha-synuclein; cultured human muscle; inclusion-body myositis; necrotic muscle fibers; neuromuscular junctions; regenerating muscle fibers;
D O I
10.1093/jnen/59.7.592
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
alpha-synuclein (alpha-syn) is an important component of neuronal and glial inclusions in brains of patients with several neurodegenerative disorders. Sporadic inclusion-body myositis (s-IBM) is the most common progressive muscle disease of older patients. Its muscle phenotype shows several similarities with Alzheimer disease brain. a distinct feature of s-IBM pathology is specific vacuolar degeneration of muscle fibers characterized by intracellular amyloid inclusions formed by both amyloid-beta (A beta) and paired-helical filaments composed of phosphorylated tau. We immunostained alpha-syn in muscle biopsies of s-IBM, disease-control, and normal patients. Approximately 60% of A beta-positive vacuolated muscle fibers (VMF) contained well-defined inclusions immunoreactive with antibodies against alpha-syn. In those fibers, alpha-syn co-localized with A beta, both by light microscopy, and ultrastructurally. Paired-helical filaments did not contain alpha-syn immunoreactivity. In all muscle biopsies, alpha-syn was strongly immunoreactive at the postsynaptic region of the neuromuscular junctions, alpha-syn immunoreactivity also occurred diffusely in regenerating and necrotic muscle fibers. In cultured human muscle fibers, alpha-syn and its mRNA were expressed by immunocytochemistry, immunoblots, and Northern blots. Our study provides the first demonstration that alpha-syn participates in normal and pathologic processes of human muscle. Therefore, its function is not exclusive to the brain and neurodegenerative diseases.
引用
收藏
页码:592 / 598
页数:7
相关论文
共 45 条
[21]   THE CORE ALZHEIMERS PEPTIDE NAC FORMS AMYLOID FIBRILS WHICH SEED AND ARE SEEDED BY BETA-AMYLOID - IS NAC A COMMON TRIGGER OR TARGET IN NEURODEGENERATIVE DISEASE [J].
HAN, HY ;
WEINREB, PH ;
LANSBURY, PT .
CHEMISTRY & BIOLOGY, 1995, 2 (03) :163-169
[22]   Oxidative stress induces amyloid-like aggregate formation of NACP/α-synuclein in vitro [J].
Hashimoto, M ;
Hsu, LJ ;
Xia, Y ;
Takeda, A ;
Sisk, A ;
Sundsmo, M ;
Masliah, E .
NEUROREPORT, 1999, 10 (04) :717-721
[23]   NACP, a synaptic protein involved in Alzheimer's disease, is differentially regulated during megakaryocyte differentiation [J].
Hashimoto, M ;
Yoshimoto, M ;
Sisk, A ;
Hsu, LJ ;
Sundsmo, M ;
Kittel, A ;
Saitoh, T ;
Miller, A ;
Masliah, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 237 (03) :611-616
[24]   Human recombinant NACP/α-synuclein is aggregated and fibrillated in vitro:: Relevance for Lewy body disease [J].
Hashimoto, M ;
Hsu, LJ ;
Sisk, A ;
Xia, Y ;
Takeda, A ;
Sundsmo, M ;
Masliah, E .
BRAIN RESEARCH, 1998, 799 (02) :301-306
[25]   NON-A-BETA COMPONENT OF ALZHEIMERS-DISEASE AMYLOID (NAC) IS AMYLOIDOGENIC [J].
IWAI, A ;
YOSHIMOTO, M ;
MASLIAH, E ;
SAITOH, T .
BIOCHEMISTRY, 1995, 34 (32) :10139-10145
[26]   IDENTIFICATION OF 2 DISTINCT SYNUCLEINS FROM HUMAN BRAIN [J].
JAKES, R ;
SPILLANTINI, MG ;
GOEDERT, M .
FEBS LETTERS, 1994, 345 (01) :27-32
[27]   Binding of A beta to alpha- and beta-synucleins: Identification of segments in alpha-synuclein/NAC precursor that bind A beta and NAC [J].
Jensen, PH ;
Hojrup, P ;
Hager, H ;
Nielsen, MS ;
Jacobsen, L ;
Olesen, OF ;
Gliemann, J ;
Jakes, R .
BIOCHEMICAL JOURNAL, 1997, 323 :539-546
[28]   RESIDUES IN THE SYNUCLEIN CONSENSUS MOTIF OF THE ALPHA-SYNUCLEIN FRAGMENT, NAC, PARTICIPATE IN TRANSGLUTAMINASE-CATALYZED CROSS-LINKING TO ALZHEIMER-DISEASE AMYLOID BETA-A4 PEPTIDE [J].
JENSEN, PH ;
SORENSEN, ES ;
PETERSEN, TE ;
GLIEMANN, J ;
RASMUSSEN, LK .
BIOCHEMICAL JOURNAL, 1995, 310 :91-94
[29]   The synuclein family [J].
Lavedan, C .
GENOME RESEARCH, 1998, 8 (09) :871-880
[30]   Comparisons of the NACP self-oligomerizations induced by Aβ25-35 in the presence of dicyclohexylcarbodiimide and N-(ethoxycarbonyl)-2-ethoxy-1,2-dihydroquinoline [J].
Lee, JH ;
Shin, HJ ;
Chang, CS ;
Paik, SR .
NEUROCHEMICAL RESEARCH, 1998, 23 (11) :1427-1434