期刊
EXPERIMENTAL GERONTOLOGY
卷 44, 期 3, 页码 228-235出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exger.2008.10.002
关键词
Innate immunity; Life span; Bacteria; Aging
资金
- Department of Health and Human Services [AG11833]
- NSF CAREER Award [MCB-0237975]
Immune function declines with age in Drosophila and humans, and autophagy is implicated in immune function. In addition, autophagy genes are required for life span extension caused by reduced insulin/IGF1-like signaling and dietary restriction in Caenorhabditis elegans. To test if the autophagy pathway might be limiting for immunity and/or life span in adult Drosophila, the Geneswitch system was used to cause conditional inactivation of the autophagy genes Atg5, Atg7 and Atg12 by RNAi. Conditional inhibition of Atg genes in adult flies reduced lysotracker staining of adult tissues, and reduced resistance to injected Escherichia coli, as evidenced by increased bacterial titers and reduced fly survival. However, survival of uninjected flies was unaffected by Atg gene inactivation. The data indicate that Atg gene activity is required for normal immune function in adult flies, and suggest that neither autophagy nor immune function are limiting for adult life span under typical laboratory conditions. (C) 2008 Elsevier Inc. All rights reserved.
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