Skin-derived fibroblasts from long-lived species are resistant to some, but not all, lethal stresses and to the mitochondrial inhibitor rotenone

被引:119
作者
Harper, James M.
Salmon, Adam B.
Leiser, Scott F.
Galecki, Andrzej T.
Miller, Richard A.
机构
[1] Univ Michigan, Sch Med, Geriatr Ctr, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI USA
[3] Univ Michigan, Sch Med, Cell & Mol Biol Program, Ann Arbor, MI USA
[4] Univ Michigan, Sch Med, VA Med Ctr, Ann Arbor, MI USA
关键词
evolution; fibroblast; longevity; oxidation; stress; LIFE-SPAN; DNA-REPAIR; DWARF MICE; CAENORHABDITIS-ELEGANS; NUCLEAR GENES; PHYLOGENETIC ANALYSIS; CONFIDENCE-INTERVALS; CELLULAR-RESISTANCE; OXIDATIVE DAMAGE; EXCISION-REPAIR;
D O I
10.1111/j.1474-9726.2006.00255.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fibroblast cell lines were developed from skin biopsies of eight species of wild-trapped rodents, one species of bat, and a group of genetically heterogeneous laboratory mice. Each cell line was tested in vitro for their resistance to six varieties of lethal stress, as well as for resistance to the nonlethal metabolic effects of the mitochondrial inhibitor rotenone and of culture at very low glucose levels. Standard linear regression of species-specific lifespan against each species mean stress resistance showed that longevity was associated with resistance to death induced by cadmium and hydrogen peroxide, as well as with resistance to rotenone inhibition. A multilevel regression method supported these associations, and suggested a similar association for resistance to heat stress. Regressions for resistance to cadmium, peroxide, heat, and rotenone remained significant after various statistical adjustments for body weight. In contrast, cells from longer-lived species did not show significantly greater resistance to ultraviolet light, paraquat, or the DNA alkylating agent methylmethanesulfonate. There was a strong correlation between species longevity and resistance to the metabolic effects of low-glucose medium among the rodent cell lines, but this test did not distinguish mice and rats from the much longer-lived little brown bat. These results are consistent with the idea that evolution of long-lived species may require development of cellular resistance to several forms of lethal injury, and provide justification for evaluation of similar properties in a much wider range of mammals and bird species.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 66 条
  • [1] Abouheif E, 1999, EVOL ECOL RES, V1, P895
  • [2] Higher-level systematics of rodents and divergence time estimates based on two congruent nuclear genes
    Adkins, RM
    Walton, AH
    Honeycutt, RL
    [J]. MOLECULAR PHYLOGENETICS AND EVOLUTION, 2003, 26 (03) : 409 - 420
  • [3] A new phylogenetic marker, apolipoprotein B, provides compelling evidence for eutherian relationships
    Amrine-Madsen, H
    Koepfli, KP
    Wayne, RK
    Springer, MS
    [J]. MOLECULAR PHYLOGENETICS AND EVOLUTION, 2003, 28 (02) : 225 - 240
  • [4] Austad S.N., 1991, J GERONTOLOGY B, V46, P47
  • [5] Diverse aging rates in metazoans: targets for functional genomics
    Austad, SN
    [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 2005, 126 (01) : 43 - 49
  • [6] Genes that prolong life: Relationships of growth hormone and growth to aging and life span
    Bartke, A
    Coshigano, K
    Kopchick, J
    Chandrashekar, V
    Mattison, J
    Kinney, B
    Hauck, S
    [J]. JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2001, 56 (08): : B340 - B349
  • [7] Berridge M.V., 1996, Biochemica, P14, DOI DOI 10.1155/2013/420601
  • [8] Testing for phylogenetic signal in comparative data: Behavioral traits are more labile
    Blomberg, SP
    Garland, T
    Ives, AR
    [J]. EVOLUTION, 2003, 57 (04) : 717 - 745
  • [9] Dwarf mice and the ageing process
    BrownBorg, HM
    Borg, KE
    Meliska, CJ
    Bartke, A
    [J]. NATURE, 1996, 384 (6604) : 33 - 33
  • [10] MECHANISM OF PARAQUAT TOXICITY IN MICE AND RATS
    BUS, JS
    CAGEN, SZ
    OLGAARD, M
    GIBSON, JE
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1976, 35 (03) : 501 - 513