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...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-09-01
|
Series: | Cells |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4409/10/9/2479 |
id |
doaj-df6b01c204504ec6bb493cef435ab8fa |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT alysonsujkowski exerciseandsestrinmediatespeedandlysosomalactivityinidrosophilaibypartiallyoverlappingmechanisms AT robertwessells exerciseandsestrinmediatespeedandlysosomalactivityinidrosophilaibypartiallyoverlappingmechanisms |
_version_ |
1717367711157190656 |