Realized immune response is enhanced in long-lived puc and chico mutants but is unaffected by dietary restriction

被引:82
作者
Libert, Sergiy
Chao, Yufang
Zwiener, Jessica
Pletcher, Scott D.
机构
[1] Baylor Coll Med, Program Cell & Mol Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Huffington Ctr Aging, Houston, TX 77030 USA
关键词
innate immunity; drosophila melanogaster; insulin signaling; chico; puc; aging; longevity; pathogen resistance; NF-kappa-B; lifespan; healthspan;
D O I
10.1016/j.molimm.2007.06.353
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The immune system is vital for the immediate survival of multicellular organisms by protecting them from the damaging effects of bacterial infections, viruses, and toxic molecules. It has been hypothesized that the immune system plays a pivotal role in determining longevity. We investigated the efficiency of the innate immune system in Drosophila carrying the longevity extending mutations puc (JNK signaling pathway, stress response) and chico (insulin signaling pathway), as well as animals subjected to dietary restriction (DR), which also extends lifespan. We found that puc heterozygous animals, as well as chico homozygous and heterozygous flies, have enhanced pathogen resistance. Surprisingly, diet manipulation did not reproducibly alter pathogen resistance, despite its significant effect on the expression of many immunity-related genes. Considering that chronic or frequent activation of the immune system results in reduced longevity, we postulate that the longevity extending potential of the above mutations may be partially obscured by parallel activation of the immune system. Such upregulation is not observed during DR, suggesting the presence of a mechanism that suppresses immune activity in diet-restricted animals. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:810 / 817
页数:8
相关论文
共 23 条
[11]  
Junger Martin A, 2003, J Biol, V2, P20, DOI 10.1186/1475-4924-2-20
[12]   The Drosophila melanogaster toll pathway participates in resistance to infection by the gram-negative human pathogen Pseudomonas aeruginosa [J].
Lau, GW ;
Goumnerov, BC ;
Walendziewicz, CL ;
Hewitson, J ;
Xiao, WZ ;
Mahajan-Miklos, S ;
Tompkins, RG ;
Perkins, LA ;
Rahme, LG .
INFECTION AND IMMUNITY, 2003, 71 (07) :4059-4066
[13]   Drosophila melanogaster Thor and response to Candida albicans infection [J].
Levitin, A. ;
Marcil, A. ;
Tettweiler, G. ;
Laforest, M. J. ;
Oberholzer, U. ;
Alarco, A. M. ;
Thomas, D. Y. ;
Lasko, P. ;
Whiteway, M. .
EUKARYOTIC CELL, 2007, 6 (04) :658-663
[14]   Trade-offs between longevity and pathogen resistance in Drosophila melanogaster are mediated by NFκB signaling [J].
Libert, Sergiy ;
Chao, Yufang ;
Chu, Xiaowen ;
Pletcher, Scott D. .
AGING CELL, 2006, 5 (06) :533-543
[15]   Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans [J].
Murphy, CT ;
McCarroll, SA ;
Bargmann, CI ;
Fraser, A ;
Kamath, RS ;
Ahringer, J ;
Li, H ;
Kenyon, C .
NATURE, 2003, 424 (6946) :277-284
[16]   Dietary restriction in Drosophila [J].
Partridge, L ;
Piper, MDW ;
Mair, W .
MECHANISMS OF AGEING AND DEVELOPMENT, 2005, 126 (09) :938-950
[17]   Flies and their Golden Apples:: The effect of dietary restriction on Drosophila aging and age-dependent gene expression [J].
Pletcher, SD ;
Libert, S ;
Skorupa, D .
AGEING RESEARCH REVIEWS, 2005, 4 (04) :451-480
[18]   Genome-wide transcript profiles in aging and calorically restricted Drosophila melanogaster [J].
Pletcher, SD ;
Macdonald, SJ ;
Marguerie, R ;
Certa, U ;
Stearns, SC ;
Goldstein, DB ;
Partridge, L .
CURRENT BIOLOGY, 2002, 12 (09) :712-723
[19]   The myth and reality of reversal of aging by hormesis [J].
Sonneborn, JS .
REVERSAL OF AGING: RESETTING THE PINEAL CLOCK, 2005, 1057 :165-176
[20]   p38 MAPK regulates expression of immune response genes and contributes to longevity in C. elegans [J].
Troemel, Emily R. ;
Chu, Stephanie W. ;
Reinke, Valerie ;
Lee, Siu Sylvia ;
Ausubel, Frederick M. ;
Kim, Dennis H. .
PLOS GENETICS, 2006, 2 (11) :1725-1739