Age-associated changes in mitochondrial parameters on peripheral human lymphocytes

被引:39
作者
Drouet, M [1 ]
Lauthier, F
Charmes, JP
Sauvage, P
Ratinaud, MH
机构
[1] Fac Med, Equipe Postulante Ctr Natl Rech Sci 118, Limoges, France
[2] Fac Sci, Limoges, France
[3] Ctr Hosp Reg Univ Dupuytren, Serv Geriatrie, F-87043 Limoges, France
关键词
aging; cytochrome c oxidase; decylubiquinol cytochrome c oxidoreductase; lymphocyte subpopulations; mtDNA; oxidoreductase activities; succinate cylochrome c reductase;
D O I
10.1016/S0531-5565(99)00058-3
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Among theories of aging, mitochondria are believed to be involved in senescence. Alterations of respiratory chain function and accumulation of various mitochondrial DNA mutations have been reported in mammalian postmitotic tissues. Because mitochondria have a central role in apoptosis and in adenosine triphosphate production, alteration of mitochondria function could contribute to immune senescence. We searched for alterations of mitochondrial parameters in peripheral lymphocytes with aging. Comparisons of respiratory chain activities of complex II+III, III, and IV were carried out in two populations of healthy volunteers with average ages of 35.3 +/- 6.7 years and 80.8 +/- 8.7 years. No difference was observed in complex IV activity between each group, whereas a significant decrease of complex II+III and a nonsignificant decrease of complex In, activity were observed with aging. Alterations in mitochondrial functions can result from mutations in mitochondrial DNA (mtDNA), the most common being the 4977-bp deletion (mtDNA(-4977)). In either group we observed many deletions of mtDNA on peripheral blood lymphocytes by large-fragment polymerase chain reaction. This result suggests that alterations of respiratory chain activities observed with aging in lymphocytes could be the result of nuclear DNA dysfunction, with consequences on immune function (reduced responsiveness to antigen). Its possible implication on the recent observation of increased apoptosis of CD45RA+RO- T cells with aging is discussed. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:843 / 852
页数:10
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