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PMID: 17681604 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

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

Molecular immunology ·Vol. 45 ·No. 3 ·2008-02-00 ·Pages 810-7

Libert S, Chao Y, Zwiener J, Pletcher SD

Abstract

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.

MeSH Terms
Animals Caloric Restriction Drosophila Proteins/genetics,immunology Drosophila melanogaster Immunity, Innate/genetics Insulin Receptor Substrate Proteins Intracellular Signaling Peptides and Proteins/genetics,immunology Longevity/genetics,immunology Mutation Phosphoprotein Phosphatases/genetics,immunology
Chemicals
Drosophila Proteins Insulin Receptor Substrate Proteins Intracellular Signaling Peptides and Proteins chico protein, Drosophila puc protein, Drosophila Phosphoprotein Phosphatases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Libert Sergiy
Program in Cell and Molecular Biology, Baylor College of Medicine, One Baylor Plaza, N820, Houston TX, 77030, United States. sergiy.libert@bcm.tmc.edu
Chao Yufang
Zwiener Jessica
Pletcher Scott D
Article Info
Journal
Molecular immunology
Abbr.
Mol Immunol
ISSN
0161-5890
Published
2008-02-00
Epub
2007-00-02
Pages
810-7
Language
English
Region
England
NLM ID
7905289
Subset
IM
Grants
NIA NIH HHS · R01AG023166 · United States
NIA NIH HHS · R21AG028298 · United States
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