Longevity and Age-Related Pathology of Mice Deficient in Pregnancy-Associated Plasma Protein-A

被引:81
作者
Conover, Cheryl A. [1 ]
Bale, Laurie K. [1 ]
Mader, Jessica R. [1 ]
Mason, Megan A. [1 ]
Keenan, Kevin P. [2 ]
Marler, Ronald J. [3 ]
机构
[1] Mayo Clin, Dept Med, Div Endocrinol & Metab, Rochester, MN 55905 USA
[2] Charles River Labs, Frederick, MD USA
[3] Mayo Clin, Dept Comparat Med, Scottsdale, AZ USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2010年 / 65卷 / 06期
关键词
Longevity; Pathology; Pregnancy-associated plasma protein-A; Insulin-like growth factor I; Mouse model; FATAL NEOPLASTIC DISEASES; FACTOR-I IGF-1; LIFE-SPAN; DWARF MICE; DELAYED OCCURRENCE; GROWTH; INSULIN; RESISTANCE; DELETION; NULL;
D O I
10.1093/gerona/glq032
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
The pregnancy-associated plasma protein-A knockout (PAPP-A KO) mouse is a model of reduced local insulin-like growth factor (IGF)-I activity with normal circulating IGF-I levels. In this study, PAPP-A KO mice had significantly increased mean (27%), median (27%), and maximum (35%) life span compared with wild-type (WT) littermates. End-of-life pathology indicated that the incidence of neoplastic disease was not significantly different in the two groups of mice; however, it occurred in older aged PAPP-A KO compared with WT mice. Furthermore, PAPP-A KO mice were less likely to show degenerative changes of age. Scheduled pathologies at 78, 104, and 130 weeks of age indicated that WT mice, in general, had more degenerative changes and tumors earlier than PAPP-A KO mice. This was particularly true for abnormalities in heart, testes, brain, kidney, spleen, and thymus. In summary, the major contributors to the extended life span of PAPP-A KO mice are delayed occurrence of fatal neoplasias and decreased incidence of age-related degenerative changes.
引用
收藏
页码:590 / 599
页数:10
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