Exercise and Sestrin Mediate Speed and Lysosomal Activity in <i>Drosophila</i> by Partially Overlapping Mechanisms

Chronic exercise is widely recognized as an important contributor to healthspan in humans and in diverse animal models. Recently, we have demonstrated that Sestrins, a family of evolutionarily conserved exercise-inducible proteins, are critical mediators of exercise benefits in flies and mice. Knock...

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Main Authors: Alyson Sujkowski, Robert Wessells
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/9/2479
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spelling doaj-df6b01c204504ec6bb493cef435ab8fa2021-09-25T23:53:24ZengMDPI AGCells2073-44092021-09-01102479247910.3390/cells10092479Exercise and Sestrin Mediate Speed and Lysosomal Activity in <i>Drosophila</i> by Partially Overlapping MechanismsAlyson Sujkowski0Robert Wessells1Department of Physiology, School of Medicine, Wayne State University, Detroit, MI 48201, USADepartment of Physiology, School of Medicine, Wayne State University, Detroit, MI 48201, USAChronic exercise is widely recognized as an important contributor to healthspan in humans and in diverse animal models. Recently, we have demonstrated that Sestrins, a family of evolutionarily conserved exercise-inducible proteins, are critical mediators of exercise benefits in flies and mice. Knockout of Sestrins prevents exercise adaptations to endurance and flight in <i>Drosophila</i>, and similarly prevents benefits to endurance and metabolism in exercising mice. In contrast, overexpression of dSestrin in muscle mimics several of the molecular and physiological adaptations characteristic of endurance exercise. Here, we extend those observations to examine the impact of dSestrin on preserving speed and increasing lysosomal activity. We find that dSestrin is a critical factor driving exercise adaptations to climbing speed, but is not absolutely required for exercise to increase lysosomal activity in <i>Drosophila</i>. The role of Sestrin in increasing speed during chronic exercise requires both the TORC2/AKT axis and the PGC1α homolog <i>spargel</i>, while dSestrin requires interactions with TORC1 to cell-autonomously increase lysosomal activity. These results highlight the conserved role of Sestrins as key factors that drive diverse physiological adaptations conferred by chronic exercise.https://www.mdpi.com/2073-4409/10/9/2479Sestrinexercise<i>Drosophila</i>
collection DOAJ
language English
format Article
sources DOAJ
author Alyson Sujkowski
Robert Wessells
spellingShingle Alyson Sujkowski
Robert Wessells
Exercise and Sestrin Mediate Speed and Lysosomal Activity in <i>Drosophila</i> by Partially Overlapping Mechanisms
Cells
Sestrin
exercise
<i>Drosophila</i>
author_facet Alyson Sujkowski
Robert Wessells
author_sort Alyson Sujkowski
title Exercise and Sestrin Mediate Speed and Lysosomal Activity in <i>Drosophila</i> by Partially Overlapping Mechanisms
title_short Exercise and Sestrin Mediate Speed and Lysosomal Activity in <i>Drosophila</i> by Partially Overlapping Mechanisms
title_full Exercise and Sestrin Mediate Speed and Lysosomal Activity in <i>Drosophila</i> by Partially Overlapping Mechanisms
title_fullStr Exercise and Sestrin Mediate Speed and Lysosomal Activity in <i>Drosophila</i> by Partially Overlapping Mechanisms
title_full_unstemmed Exercise and Sestrin Mediate Speed and Lysosomal Activity in <i>Drosophila</i> by Partially Overlapping Mechanisms
title_sort exercise and sestrin mediate speed and lysosomal activity in <i>drosophila</i> by partially overlapping mechanisms
publisher MDPI AG
series Cells
issn 2073-4409
publishDate 2021-09-01
description Chronic exercise is widely recognized as an important contributor to healthspan in humans and in diverse animal models. Recently, we have demonstrated that Sestrins, a family of evolutionarily conserved exercise-inducible proteins, are critical mediators of exercise benefits in flies and mice. Knockout of Sestrins prevents exercise adaptations to endurance and flight in <i>Drosophila</i>, and similarly prevents benefits to endurance and metabolism in exercising mice. In contrast, overexpression of dSestrin in muscle mimics several of the molecular and physiological adaptations characteristic of endurance exercise. Here, we extend those observations to examine the impact of dSestrin on preserving speed and increasing lysosomal activity. We find that dSestrin is a critical factor driving exercise adaptations to climbing speed, but is not absolutely required for exercise to increase lysosomal activity in <i>Drosophila</i>. The role of Sestrin in increasing speed during chronic exercise requires both the TORC2/AKT axis and the PGC1α homolog <i>spargel</i>, while dSestrin requires interactions with TORC1 to cell-autonomously increase lysosomal activity. These results highlight the conserved role of Sestrins as key factors that drive diverse physiological adaptations conferred by chronic exercise.
topic Sestrin
exercise
<i>Drosophila</i>
url https://www.mdpi.com/2073-4409/10/9/2479
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