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Autophagic Punctum

Age-associated and tissue-specific decline in autophagic activity in the nematode C. elegans

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Pages 1276-1277 | Received 31 Jan 2018, Accepted 21 Feb 2018, Published online: 28 May 2018

Figures & data

Figure 1. Spatiotemporal analysis of autophagic activity in C. elegans. (A) Different LGG-1/Atg8 reporters were used in combination with bafilomycin A1 (BafA) to quantify fluorescent puncta as a readout for autophagosomes (AP) and/or autolysosomes (AL) to assess autophagic activity in tissues of C. elegans (i.e., intestine, pharynx [the foregut], body-wall muscle, and neurons. (B) Assessment of autophagic activity in young (top) and old wild-type (bottom) animals shows an age-associated decline. This trend was seen in all tissues, albeit with different kinetics. (C) Assessment of autophagic activity in long-lived mutants (i.e., in DAF-2/insulin/IGF-1 receptor daf-2(e1370) and GLP-1/Notch receptor glp-1(e2144) mutants) indicate a general increase in autophagic activity in young (top) and old (bottom) animals, compared to wild-type, and showed age- and tissue-specific differences between the 2 long-lived mutants. Future experiments are needed to directly test autophagic activity in C. elegans. See text for details. PG, phagophore.

Figure 1. Spatiotemporal analysis of autophagic activity in C. elegans. (A) Different LGG-1/Atg8 reporters were used in combination with bafilomycin A1 (BafA) to quantify fluorescent puncta as a readout for autophagosomes (AP) and/or autolysosomes (AL) to assess autophagic activity in tissues of C. elegans (i.e., intestine, pharynx [the foregut], body-wall muscle, and neurons. (B) Assessment of autophagic activity in young (top) and old wild-type (bottom) animals shows an age-associated decline. This trend was seen in all tissues, albeit with different kinetics. (C) Assessment of autophagic activity in long-lived mutants (i.e., in DAF-2/insulin/IGF-1 receptor daf-2(e1370) and GLP-1/Notch receptor glp-1(e2144) mutants) indicate a general increase in autophagic activity in young (top) and old (bottom) animals, compared to wild-type, and showed age- and tissue-specific differences between the 2 long-lived mutants. Future experiments are needed to directly test autophagic activity in C. elegans. See text for details. PG, phagophore.

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