MYOCLONIC EPILEPSY WITH RAGGED-RED FIBERS (MERRF) - AN IMMUNOHISTOCHEMICAL STUDY OF THE BRAIN

被引:27
作者
SPARACO, M [1 ]
SCHON, EA [1 ]
DIMAURO, S [1 ]
BONILLA, E [1 ]
机构
[1] COLUMBIA UNIV,COLL PHYS & SURG,DEPT NEUROL,NEW YORK,NY 10032
关键词
D O I
10.1111/j.1750-3639.1995.tb00586.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Myoclonic epilepsy with ragged-red fibers (MERRF) is a maternally inherited disorder of oxidative phosphorylation due to specific point mutations within the mitochondrial tRNA(Lys) gene. Mitochondrial dysfunction in the central nervous system (CNS) of patients with MERRF accounts for the neurological manifestations of the disease. Antibodies against subunits of complex I, III, IV and V of the respiratory chain were used to study the expression of these proteins in the frontal cortex, cerebellum and medulla from an autoptic case of MERRF. We found a selective decreased expression of subunit II of cytochrome c oxidase (COX-II) in these regions. Immunohistochemical abnormalities were more widespread than the lesions described by traditional histopathological techniques and made possible an attempt of explanation for the neurological symptoms of the patient.
引用
收藏
页码:125 / 133
页数:9
相关论文
共 44 条
[1]   REGULATION OF MITOCHONDRIAL GENE-EXPRESSION IN MAMMALIAN-CELLS [J].
ATTARDI, G ;
CHOMYN, A ;
KING, MP ;
KRUSE, B ;
POLOSA, PL ;
MURDTER, NN .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1990, 18 (04) :509-513
[2]   IMMUNOCYTOCHEMICAL DEMONSTRATION OF CYTOCHROME-C OXIDASE WITH AN IMMUNOPEROXIDASE METHOD - A SPECIFIC STAIN FOR MITOCHONDRIA IN FORMALIN-FIXED AND PARAFFIN-EMBEDDED HUMAN-TISSUES [J].
BEDETTI, CD .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1985, 33 (05) :446-452
[3]   CLINICAL SPECTRUM OF MITOCHONDRIAL-DNA MUTATION AT BASE PAIR-8344 [J].
BERKOVIC, SF ;
SHOUBRIDGE, EA ;
ANDERMANN, F ;
ANDERMANN, E ;
CARPENTER, S ;
KARPATI, G .
LANCET, 1991, 338 (8764) :457-457
[4]   MYOCLONUS EPILEPSY AND RAGGED-RED FIBERS (MERRF) .1. A CLINICAL, PATHOLOGICAL, BIOCHEMICAL, MAGNETIC-RESONANCE SPECTROGRAPHIC AND POSITRON EMISSION TOMOGRAPHIC STUDY [J].
BERKOVIC, SF ;
CARPENTER, S ;
EVANS, A ;
KARPATI, G ;
SHOUBRIDGE, EA ;
ANDERMANN, F ;
MEYER, E ;
TYLER, JL ;
DIKSIC, M ;
ARNOLD, D ;
WOLFE, LS ;
ANDERMANN, E ;
HAKIM, AM .
BRAIN, 1989, 112 :1231-1260
[5]  
BOULET L, 1992, AM J HUM GENET, V51, P1187
[6]   INVITRO GENETIC TRANSFER OF PROTEIN-SYNTHESIS AND RESPIRATION DEFECTS TO MITOCHONDRIAL DNA-LESS CELLS WITH MYOPATHY-PATIENT MITOCHONDRIA [J].
CHOMYN, A ;
MEOLA, G ;
BRESOLIN, N ;
LAI, ST ;
SCARLATO, G ;
ATTARDI, G .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (04) :2236-2244
[7]   DDT MYOCLONUS - SITES AND MECHANISM OF ACTION [J].
CHUNG, EY ;
VANWOERT, MH .
EXPERIMENTAL NEUROLOGY, 1984, 85 (02) :273-282
[8]  
DIMAURO S, 1993, MOL CELLULAR APPROAC, P67
[9]   PHOSPHORUS MAGNETIC-RESONANCE SPECTROSCOPY OF PATIENTS WITH MITOCHONDRIAL CYTOPATHIES DEMONSTRATES DECREASED LEVELS OF BRAIN PHOSPHOCREATINE [J].
ELEFF, SM ;
BARKER, PB ;
BLACKBAND, SJ ;
CHATHAM, JC ;
LUTZ, NW ;
JOHNS, DR ;
BRYAN, RN ;
HURKO, O .
ANNALS OF NEUROLOGY, 1990, 27 (06) :626-630
[10]   MYOCLONUS EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS (MITOCHONDRIAL ABNORMALITIES) - DISEASE ENTITY OR A SYNDROME - LIGHT-MICROSCOPIC AND ELECTRON-MICROSCOPIC STUDIES OF 2 CASES AND REVIEW OF LITERATURE [J].
FUKUHARA, N ;
TOKIGUCHI, S ;
SHIRAKAWA, K ;
TSUBAKI, T .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1980, 47 (01) :117-133