IMMUNOHISTOCHEMICAL STUDIES ON COMPLEX-I, COMPLEX-II, COMPLEX-III, AND COMPLEX-IV OF MITOCHONDRIA IN PARKINSONS-DISEASE

被引:257
作者
HATTORI, N
TANAKA, M
OZAWA, T
MIZUNO, Y
机构
[1] JUNTENDO UNIV,SCH MED,DEPT NEUROL,2-1-1 HONGO,BUNKYO KU,TOKYO 113,JAPAN
[2] NAGOYA UNIV,FAC MED,DEPT BIOMED CHEM,NAGOYA,AICHI 464,JAPAN
关键词
D O I
10.1002/ana.410300409
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We examined the substantia nigra of 8 patients with Parkinson's disease immunohistochemically using antisera against complexes I, II, III, and IV of the mitochondrial electron transport system. In the patients with Parkinson's disease, a fair proportion of the nigral neurons showed reduced staining against the complex I antibody. The proportion of the neurons with reduced staining ranged from 12.7 to 74.1% of the melanized nigral neurons. Although neurons with reduced immunostaining for complex I were also observed in control subjects, the proportion among the nigral neurons was significantly smaller than in parkinsonian patients. Staining for complexes III and IV appeared normal. Staining of substantia nigra for complex II was decreased in 3 parkinsonian patients. These results are consistent with our findings that there is a deletion of gene coding for the four subunits in the mitochondrial DNA located in the striata of parkinsonian patients.
引用
收藏
页码:563 / 571
页数:9
相关论文
共 50 条
  • [31] MITOCHONDRIAL COMPLEX I DEFICIENCY IN PARKINSONS-DISEASE
    SCHAPIRA, AHV
    COOPER, JM
    DEXTER, D
    JENNER, P
    CLARK, JB
    MARSDEN, CD
    LANCET, 1989, 1 (8649) : 1269 - 1269
  • [32] MITOCHONDRIAL COMPLEX I DEFICIENCY IN PARKINSONS-DISEASE
    SCHAPIRA, AHV
    COOPER, JM
    DEXTER, D
    CLARK, JB
    JENNER, P
    MARSDEN, CD
    JOURNAL OF NEUROCHEMISTRY, 1990, 54 (03) : 823 - 827
  • [33] DEFECTS OF COMPLEX-I AND COMPLEX-IV IN SKELETAL-MUSCLE FROM PATIENTS WITH CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA
    SHERRATT, HSA
    JOHNSON, MA
    TURNBULL, DM
    ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1986, 488 : 508 - 510
  • [34] MITOCHONDRIAL-DNA COMPLEX-I AND COMPLEX-III MUTATIONS ASSOCIATED WITH LEBER HEREDITARY OPTIC NEUROPATHY
    BROWN, MD
    VOLJAVEC, AS
    LOTT, MT
    TORRONI, A
    YANG, CC
    WALLACE, DC
    GENETICS, 1992, 130 (01) : 163 - 173
  • [35] MITOCHONDRIAL TRANSFER RNA(THR) MUTATION IN FATAL INFANTILE MYOPATHY WITH DEFICIENCY OF THE RESPIRATORY COMPLEX-I AND COMPLEX-IV
    TIRANTI, V
    FABRIZI, GM
    MARIOTTI, C
    SAVARESE, N
    UZIEL, G
    DIDONATO, S
    ZEVIANI, M
    NEUROLOGY, 1993, 43 (04) : A284 - A284
  • [36] CARDIOLIPIN REQUIREMENT FOR ELECTRON-TRANSFER IN COMPLEX-I AND COMPLEX-III OF THE MITOCHONDRIAL RESPIRATORY-CHAIN
    FRY, M
    GREEN, DE
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1981, 256 (04) : 1874 - 1880
  • [37] NORMAL MITOCHONDRIAL GENOME IN BRAIN FROM PATIENTS WITH PARKINSONS-DISEASE AND COMPLEX-I DEFECT
    LESTIENNE, P
    NELSON, J
    RIEDERER, P
    JELLINGER, K
    REICHMANN, H
    JOURNAL OF NEUROCHEMISTRY, 1990, 55 (05) : 1810 - 1812
  • [38] Inhibition of complex-II of the mitochondrial electron transport chain leads to complex-I dysfunction in rats: relevance to Huntington's disease
    Pandey, M.
    Varghese, M.
    Sen, S.
    Sindhu, K. M.
    Mohanakumar, K. P.
    Usha, R.
    JOURNAL OF NEUROCHEMISTRY, 2006, 98 : 26 - 26
  • [39] POTENTIOMETRIC STUDIES ON YEAST COMPLEX-III
    TSAI, AL
    PALMER, G
    BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 722 (02) : 349 - 363
  • [40] ANATOMIC AND DISEASE SPECIFICITY OF NADH COQ1 REDUCTASE (COMPLEX-I) DEFICIENCY IN PARKINSONS-DISEASE
    SCHAPIRA, AHV
    MANN, VM
    COOPER, JM
    DEXTER, D
    DANIEL, SE
    JENNER, P
    CLARK, JB
    MARSDEN, CD
    JOURNAL OF NEUROCHEMISTRY, 1990, 55 (06) : 2142 - 2145