TY - JOUR
T1 - Chapter Twenty‐Nine Monitoring the Role of Autophagy in C. elegans Aging
AU - Meléndez, Alicia
AU - Hall, David H.
AU - Hansen, Malene
N1 - Funding Information:
This study was funded by the National Institute of Nursing Research, Grant Number NR 04416, as well as partial support from grants MHR01 51019, GCRC RR00046, P30 A150410, and NR P3003962. The authors also gratefully acknowledge Donna Harris, RN, BSN, who assisted in this study.
PY - 2008/1/1
Y1 - 2008/1/1
N2 - Autophagy plays crucial roles in many biological processes, and recent research points to a possibly conserved role for autophagy in the process of organismal aging. Experiments in the nematode C. elegans suggest that autophagy may be required specifically for longevity pathways that are regulated by environmental signals. Known longevity genes can be assigned to four major longevity pathways/processes: insulin/IGF‐1 signaling, dietary restriction, protein translation, and mitochondrial respiration. Of these, reduced insulin/IGF‐1 signaling and dietary restriction, but not protein translation inhibition, appear to rely on autophagy to increase life span. Multiple experimental approaches have been used to study autophagy in the context of aging in C. elegans. This chapter describes techniques used to address the link between aging and autophagy in C. elegans. Specifically, we summarize how to examine organismal life span in various longevity mutants and how to visually detect autophagy and autolysosomal formation in C. elegans.
AB - Autophagy plays crucial roles in many biological processes, and recent research points to a possibly conserved role for autophagy in the process of organismal aging. Experiments in the nematode C. elegans suggest that autophagy may be required specifically for longevity pathways that are regulated by environmental signals. Known longevity genes can be assigned to four major longevity pathways/processes: insulin/IGF‐1 signaling, dietary restriction, protein translation, and mitochondrial respiration. Of these, reduced insulin/IGF‐1 signaling and dietary restriction, but not protein translation inhibition, appear to rely on autophagy to increase life span. Multiple experimental approaches have been used to study autophagy in the context of aging in C. elegans. This chapter describes techniques used to address the link between aging and autophagy in C. elegans. Specifically, we summarize how to examine organismal life span in various longevity mutants and how to visually detect autophagy and autolysosomal formation in C. elegans.
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U2 - 10.1016/S0076-6879(08)03229-1
DO - 10.1016/S0076-6879(08)03229-1
M3 - Review article
C2 - 19185737
AN - SCOPUS:61949432569
SN - 0076-6879
VL - 451
SP - 493
EP - 520
JO - Methods in Enzymology
JF - Methods in Enzymology
IS - C
ER -