Longevity is not influenced by prenatal programming of body size.
Longevity is not influenced by prenatal programming of body size.
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DOI:
10.1111/j.1474-9726.2010.00589.x
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发表时间:
2010-08
期刊:
影响因子:
7.8
通讯作者:
Mason MA
中科院分区:
文献类型:
--
作者:
Conover CA;Bale LK;Grell JA;Mader JR;Mason MA
Insulin-like growth factor (IGF) signaling is essential for achieving optimal body size during fetal development, whereas, in the adult, IGFs are associated with aging and age-related diseases. However, it is unclear as to what extent lifespan is influenced by events that occur during development. Here we provide direct evidence that the exceptional longevity of mice with altered IGF signaling is not linked to prenatal programming of body size. Mice null for pregnancy-associated plasma protein-A (PAPP-A), an IGF binding protein proteinase that increases local IGF bioavailability, are 60–70% the size of their wild-type littermates at birth and have extended median and maximum lifespan of 30–40%. In this study, PAPP-A−/− mice whose body size was normalized during fetal development through disruption of IgfII imprinting, did not lose their longevity advantage. Adult-specific moderation of IGF signaling through PAPP-A inhibition may present a unique opportunity to improve lifespan without affecting important aspects of early life physiology.
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影响因子:
4
作者:
Bale, LK;Conover, CA
通讯作者:
Conover, CA
DOI:
10.1093/gerona/63.9.895
发表时间:
2008-09
期刊:
The journals of gerontology. Series A, Biological sciences and medical sciences
影响因子:
--
作者:
Swindell WR;Harper JM;Miller RA
通讯作者:
Miller RA
DOI:
10.1073/pnas.0705467105
发表时间:
2008-03-04
影响因子:
11.1
作者:
Suh, Yousin;Atzmon, Gil;Cohen, Pinchas
通讯作者:
Cohen, Pinchas
影响因子:
2.9
作者:
Rollo, CD
通讯作者:
Rollo, CD
影响因子:
56.9
作者:
Sutter, Nathan B.;Bustamante, Carlos D.;Ostrander, Elaine A.
通讯作者:
Ostrander, Elaine A.