Effects of an acute exercise bout in hypoxia on extracellular vesicle release in healthy and prediabetic subjects
The purpose of this study is to investigate exosome-like vesicle (ELV) plasma concentrations and markers of multivesicular body (MVB) biogenesis in skeletal muscle in response to acute exercise. Seventeen healthy [body mass index (BMI): 23.5 ± 0.5 kg·m −2 ] and 15 prediabetic (BMI: 27.3 ± 1.2 kg·m −...
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Published in | American journal of physiology. Regulatory, integrative and comparative physiology Vol. 322; no. 2; pp. R112 - R122 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Physiological Society
01.02.2022
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Subjects | |
Online Access | Get full text |
ISSN | 0363-6119 1522-1490 1522-1490 |
DOI | 10.1152/ajpregu.00220.2021 |
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Abstract | The purpose of this study is to investigate exosome-like vesicle (ELV) plasma concentrations and markers of multivesicular body (MVB) biogenesis in skeletal muscle in response to acute exercise. Seventeen healthy [body mass index (BMI): 23.5 ± 0.5 kg·m
−2
] and 15 prediabetic (BMI: 27.3 ± 1.2 kg·m
−2
) men were randomly assigned to two groups performing an acute cycling bout in normoxia or hypoxia ([Formula: see text] 14.0%). Venous blood samples were taken before (T0), during (T30), and after (T60) exercise, and biopsies from m. vastus lateralis were collected before and after exercise. Plasma ELVs were isolated by size exclusion chromatography, counted by nanoparticle tracking analysis (NTA), and characterized according to international standards, followed by expression analyses of canonical ELV markers in skeletal muscle. In the healthy normoxic group, the total number of particles in the plasma increased during exercise from T0 to T30 (+313%) followed by a decrease from T30 to T60 (−53%). In the same group, an increase in TSG101, CD81, and HSP60 protein expression was measured after exercise in plasma ELVs; however, in the prediabetic group, the total number of particles in the plasma was not affected by exercise. The mRNA content of TSG101, ALIX, and CD9 was upregulated in skeletal muscle after exercise in normoxia, whereas CD9 and CD81 were downregulated in hypoxia. ELV plasma abundance increased in response to acute aerobic exercise in healthy subjects in normoxia, but not in prediabetic subjects, nor in hypoxia. Skeletal muscle analyses suggested that this tissue did not likely play a major role of the exercise-induced increase in circulating ELVs. |
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AbstractList | The purpose of this study is to investigate exosome-like vesicle (ELV) plasma concentrations and markers of multivesicular body (MVB) biogenesis in skeletal muscle in response to acute exercise. Seventeen healthy [body mass index (BMI): 23.5 ± 0.5 kg·m
] and 15 prediabetic (BMI: 27.3 ± 1.2 kg·m
) men were randomly assigned to two groups performing an acute cycling bout in normoxia or hypoxia ([Formula: see text] 14.0%). Venous blood samples were taken before (T0), during (T30), and after (T60) exercise, and biopsies from m. vastus lateralis were collected before and after exercise. Plasma ELVs were isolated by size exclusion chromatography, counted by nanoparticle tracking analysis (NTA), and characterized according to international standards, followed by expression analyses of canonical ELV markers in skeletal muscle. In the healthy normoxic group, the total number of particles in the plasma increased during exercise from T0 to T30 (+313%) followed by a decrease from T30 to T60 (-53%). In the same group, an increase in TSG101, CD81, and HSP60 protein expression was measured after exercise in plasma ELVs; however, in the prediabetic group, the total number of particles in the plasma was not affected by exercise. The mRNA content of TSG101, ALIX, and CD9 was upregulated in skeletal muscle after exercise in normoxia, whereas CD9 and CD81 were downregulated in hypoxia. ELV plasma abundance increased in response to acute aerobic exercise in healthy subjects in normoxia, but not in prediabetic subjects, nor in hypoxia. Skeletal muscle analyses suggested that this tissue did not likely play a major role of the exercise-induced increase in circulating ELVs. The purpose of this study is to investigate exosome-like vesicle (ELV) plasma concentrations and markers of multivesicular body (MVB) biogenesis in skeletal muscle in response to acute exercise. Seventeen healthy [body mass index (BMI): 23.5 ± 0.5 kg·m −2 ] and 15 prediabetic (BMI: 27.3 ± 1.2 kg·m −2 ) men were randomly assigned to two groups performing an acute cycling bout in normoxia or hypoxia ([Formula: see text] 14.0%). Venous blood samples were taken before (T0), during (T30), and after (T60) exercise, and biopsies from m. vastus lateralis were collected before and after exercise. Plasma ELVs were isolated by size exclusion chromatography, counted by nanoparticle tracking analysis (NTA), and characterized according to international standards, followed by expression analyses of canonical ELV markers in skeletal muscle. In the healthy normoxic group, the total number of particles in the plasma increased during exercise from T0 to T30 (+313%) followed by a decrease from T30 to T60 (−53%). In the same group, an increase in TSG101, CD81, and HSP60 protein expression was measured after exercise in plasma ELVs; however, in the prediabetic group, the total number of particles in the plasma was not affected by exercise. The mRNA content of TSG101, ALIX, and CD9 was upregulated in skeletal muscle after exercise in normoxia, whereas CD9 and CD81 were downregulated in hypoxia. ELV plasma abundance increased in response to acute aerobic exercise in healthy subjects in normoxia, but not in prediabetic subjects, nor in hypoxia. Skeletal muscle analyses suggested that this tissue did not likely play a major role of the exercise-induced increase in circulating ELVs. The purpose of this study is to investigate exosome-like vesicle (ELV) plasma concentrations and markers of multivesicular body (MVB) biogenesis in skeletal muscle in response to acute exercise. Seventeen healthy [body mass index (BMI): 23.5 ± 0.5 kg·m−2] and 15 prediabetic (BMI: 27.3 ± 1.2 kg·m−2) men were randomly assigned to two groups performing an acute cycling bout in normoxia or hypoxia (FIO2 14.0%). Venous blood samples were taken before (T0), during (T30), and after (T60) exercise, and biopsies from m. vastus lateralis were collected before and after exercise. Plasma ELVs were isolated by size exclusion chromatography, counted by nanoparticle tracking analysis (NTA), and characterized according to international standards, followed by expression analyses of canonical ELV markers in skeletal muscle. In the healthy normoxic group, the total number of particles in the plasma increased during exercise from T0 to T30 (+313%) followed by a decrease from T30 to T60 (−53%). In the same group, an increase in TSG101, CD81, and HSP60 protein expression was measured after exercise in plasma ELVs; however, in the prediabetic group, the total number of particles in the plasma was not affected by exercise. The mRNA content of TSG101, ALIX, and CD9 was upregulated in skeletal muscle after exercise in normoxia, whereas CD9 and CD81 were downregulated in hypoxia. ELV plasma abundance increased in response to acute aerobic exercise in healthy subjects in normoxia, but not in prediabetic subjects, nor in hypoxia. Skeletal muscle analyses suggested that this tissue did not likely play a major role of the exercise-induced increase in circulating ELVs. The purpose of this study is to investigate exosome-like vesicle (ELV) plasma concentrations and markers of multivesicular body (MVB) biogenesis in skeletal muscle in response to acute exercise. Seventeen healthy [body mass index (BMI): 23.5 ± 0.5 kg·m-2] and 15 prediabetic (BMI: 27.3 ± 1.2 kg·m-2) men were randomly assigned to two groups performing an acute cycling bout in normoxia or hypoxia ([Formula: see text] 14.0%). Venous blood samples were taken before (T0), during (T30), and after (T60) exercise, and biopsies from m. vastus lateralis were collected before and after exercise. Plasma ELVs were isolated by size exclusion chromatography, counted by nanoparticle tracking analysis (NTA), and characterized according to international standards, followed by expression analyses of canonical ELV markers in skeletal muscle. In the healthy normoxic group, the total number of particles in the plasma increased during exercise from T0 to T30 (+313%) followed by a decrease from T30 to T60 (-53%). In the same group, an increase in TSG101, CD81, and HSP60 protein expression was measured after exercise in plasma ELVs; however, in the prediabetic group, the total number of particles in the plasma was not affected by exercise. The mRNA content of TSG101, ALIX, and CD9 was upregulated in skeletal muscle after exercise in normoxia, whereas CD9 and CD81 were downregulated in hypoxia. ELV plasma abundance increased in response to acute aerobic exercise in healthy subjects in normoxia, but not in prediabetic subjects, nor in hypoxia. Skeletal muscle analyses suggested that this tissue did not likely play a major role of the exercise-induced increase in circulating ELVs.The purpose of this study is to investigate exosome-like vesicle (ELV) plasma concentrations and markers of multivesicular body (MVB) biogenesis in skeletal muscle in response to acute exercise. Seventeen healthy [body mass index (BMI): 23.5 ± 0.5 kg·m-2] and 15 prediabetic (BMI: 27.3 ± 1.2 kg·m-2) men were randomly assigned to two groups performing an acute cycling bout in normoxia or hypoxia ([Formula: see text] 14.0%). Venous blood samples were taken before (T0), during (T30), and after (T60) exercise, and biopsies from m. vastus lateralis were collected before and after exercise. Plasma ELVs were isolated by size exclusion chromatography, counted by nanoparticle tracking analysis (NTA), and characterized according to international standards, followed by expression analyses of canonical ELV markers in skeletal muscle. In the healthy normoxic group, the total number of particles in the plasma increased during exercise from T0 to T30 (+313%) followed by a decrease from T30 to T60 (-53%). In the same group, an increase in TSG101, CD81, and HSP60 protein expression was measured after exercise in plasma ELVs; however, in the prediabetic group, the total number of particles in the plasma was not affected by exercise. The mRNA content of TSG101, ALIX, and CD9 was upregulated in skeletal muscle after exercise in normoxia, whereas CD9 and CD81 were downregulated in hypoxia. ELV plasma abundance increased in response to acute aerobic exercise in healthy subjects in normoxia, but not in prediabetic subjects, nor in hypoxia. Skeletal muscle analyses suggested that this tissue did not likely play a major role of the exercise-induced increase in circulating ELVs. |
Author | De Groote, Estelle Warnier, Geoffrey Nederveen, Joshua P. Delcorte, Ophélie Nilsson, Mats I. Britto, Florian A. Deldicque, Louise Pierreux, Christophe E. Tarnopolsky, Mark A. |
Author_xml | – sequence: 1 givenname: Geoffrey surname: Warnier fullname: Warnier, Geoffrey organization: Institute of Neuroscience, Université Catholique de Louvain, Louvain-la-Neuve, Belgium – sequence: 2 givenname: Estelle surname: De Groote fullname: De Groote, Estelle organization: Institute of Neuroscience, Université Catholique de Louvain, Louvain-la-Neuve, Belgium – sequence: 3 givenname: Florian A. surname: Britto fullname: Britto, Florian A. organization: Institute of Neuroscience, Université Catholique de Louvain, Louvain-la-Neuve, Belgium – sequence: 4 givenname: Ophélie surname: Delcorte fullname: Delcorte, Ophélie organization: CELL Unit, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium – sequence: 5 givenname: Joshua P. surname: Nederveen fullname: Nederveen, Joshua P. organization: Department of Pediatrics, McMaster University Medical Centre, Hamilton, Ontario, Canada – sequence: 6 givenname: Mats I. surname: Nilsson fullname: Nilsson, Mats I. organization: Exerkine Corporation, McMaster University Medical Centre, Hamilton, Ontario, Canada – sequence: 7 givenname: Christophe E. surname: Pierreux fullname: Pierreux, Christophe E. organization: CELL Unit, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium – sequence: 8 givenname: Mark A. surname: Tarnopolsky fullname: Tarnopolsky, Mark A. organization: Department of Pediatrics, McMaster University Medical Centre, Hamilton, Ontario, Canada, Exerkine Corporation, McMaster University Medical Centre, Hamilton, Ontario, Canada – sequence: 9 givenname: Louise orcidid: 0000-0003-3393-5278 surname: Deldicque fullname: Deldicque, Louise organization: Institute of Neuroscience, Université Catholique de Louvain, Louvain-la-Neuve, Belgium |
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Cites_doi | 10.1016/j.colsurfb.2011.05.013 10.1249/MSS.0b013e31817f1988 10.1111/j.1538-7836.2011.04610.x 10.3389/fphys.2019.00929 10.1152/ajpendo.00263.2020 10.1002/dmrr.1156 10.1242/jeb.048074 10.1113/EP088017 10.1016/j.jhep.2016.12.016 10.1007/s00421-015-3207-8 10.3389/fphys.2018.01149 10.1080/20013078.2019.1615820 10.3390/cells8070727 10.1155/2018/7807245 10.1016/j.semcdb.2017.01.002 10.1152/ajpendo.00138.2018 10.1038/srep24316 10.3389/fphys.2020.604274 10.3402/jev.v4.28239 10.1113/EP087396 10.1002/jev2.12002 10.1016/j.tma.2020.07.006 10.2337/db09-0165 10.1152/ajpendo.00172.2020 10.1038/s41598-018-35401-8 10.1080/01926230701320337 10.1249/MSS.0000000000001694 10.1096/fj.202000463R 10.1016/j.apsb.2016.02.001 10.1038/s41366-019-0460-7 10.1016/j.physbeh.2016.04.035 10.1016/j.tcb.2008.11.003 10.1371/journal.pbio.1001874 10.1080/20013078.2018.1535750 10.1371/journal.pone.0125094 10.1371/journal.pone.0027809 10.1002/mus.21945 10.3389/fphys.2018.00532 10.1002/dmrr.3107 |
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Title | Effects of an acute exercise bout in hypoxia on extracellular vesicle release in healthy and prediabetic subjects |
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