PMID- 28694500 OWN - NLM STAT- MEDLINE DCOM- 20190116 LR - 20230805 IS - 2045-2322 (Electronic) IS - 2045-2322 (Linking) VI - 7 IP - 1 DP - 2017 Jul 10 TI - Resistance exercise initiates mechanistic target of rapamycin (mTOR) translocation and protein complex co-localisation in human skeletal muscle. PG - 5028 LID - 10.1038/s41598-017-05483-x [doi] LID - 5028 AB - The mechanistic target of rapamycin (mTOR) is a central mediator of protein synthesis in skeletal muscle. We utilized immunofluorescence approaches to study mTOR cellular distribution and protein-protein co-localisation in human skeletal muscle in the basal state as well as immediately, 1 and 3 h after an acute bout of resistance exercise in a fed (FED; 20 g Protein/40 g carbohydrate/1 g fat) or energy-free control (CON) state. mTOR and the lysosomal protein LAMP2 were highly co-localised in basal samples. Resistance exercise resulted in rapid translocation of mTOR/LAMP2 towards the cell membrane. Concurrently, resistance exercise led to the dissociation of TSC2 from Rheb and increased in the co-localisation of mTOR and Rheb post exercise in both FED and CON. In addition, mTOR co-localised with Eukaryotic translation initiation factor 3 subunit F (eIF3F) at the cell membrane post-exercise in both groups, with the response significantly greater at 1 h of recovery in the FED compared to CON. Collectively our data demonstrate that cellular trafficking of mTOR occurs in human muscle in response to an anabolic stimulus, events that appear to be primarily influenced by muscle contraction. The translocation and association of mTOR with positive regulators (i.e. Rheb and eIF3F) is consistent with an enhanced mRNA translational capacity after resistance exercise. FAU - Song, Zhe AU - Song Z AD - School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, England, UK. FAU - Moore, Daniel R AU - Moore DR AD - Faculty of Kinesiology and Physical Education, University of Toronto, Toronto, Canada. AD - Human Health and Nutritional Sciences, University of Guelph, Guelph, Canada. FAU - Hodson, Nathan AU - Hodson N AD - School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, England, UK. FAU - Ward, Carl AU - Ward C AD - Institute of Cancer and Genomic Sciences, University of Birmingham, England, UK. FAU - Dent, Jessica R AU - Dent JR AD - School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, England, UK. FAU - O'Leary, Mary F AU - O'Leary MF AD - Institute of Inflammation and Ageing, University of Birmingham, England, UK. FAU - Shaw, Andrew M AU - Shaw AM AD - School of Sport, University of Stirling, Scotland, UK. FAU - Hamilton, D Lee AU - Hamilton DL AD - School of Sport, University of Stirling, Scotland, UK. FAU - Sarkar, Sovan AU - Sarkar S AD - Institute of Cancer and Genomic Sciences, University of Birmingham, England, UK. FAU - Gangloff, Yann-Gael AU - Gangloff YG AD - Institut NeuroMyoGene (INMG), University Lyon 1, INSERM U 1217, Lyon, France. FAU - Hornberger, Troy A AU - Hornberger TA AD - Department of Comparative Biosciences, The University of Wisconsin, Madison, USA. FAU - Spriet, Lawrence L AU - Spriet LL AD - Human Health and Nutritional Sciences, University of Guelph, Guelph, Canada. FAU - Heigenhauser, George J AU - Heigenhauser GJ AD - Department of Medicine, McMaster University, Hamilton, Canada. FAU - Philp, Andrew AU - Philp A AD - School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, England, UK. a.philp@bham.ac.uk. LA - eng GR - R01 AR057347/AR/NIAMS NIH HHS/United States GR - R56 AR057347/AR/NIAMS NIH HHS/United States PT - Comparative Study PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, Non-P.H.S. DEP - 20170710 PL - England TA - Sci Rep JT - Scientific reports JID - 101563288 RN - 0 (Dietary Carbohydrates) RN - 0 (Dietary Proteins) RN - 0 (EIF3F protein, human) RN - 0 (Eukaryotic Initiation Factor-3) RN - 0 (LAMP2 protein, human) RN - 0 (Lysosomal-Associated Membrane Protein 2) RN - 0 (RHEB protein, human) RN - 0 (Ras Homolog Enriched in Brain Protein) RN - 0 (TSC2 protein, human) RN - 0 (Tuberous Sclerosis Complex 2 Protein) RN - EC 2.7.1.1 (MTOR protein, human) RN - EC 2.7.11.1 (TOR Serine-Threonine Kinases) SB - IM MH - Adult MH - Cell Membrane/metabolism MH - Dietary Carbohydrates/administration & dosage MH - Dietary Proteins/administration & dosage MH - Eukaryotic Initiation Factor-3/*metabolism MH - Female MH - Humans MH - Lysosomal-Associated Membrane Protein 2/*metabolism MH - Male MH - Muscle Contraction MH - Muscle, Skeletal/*metabolism MH - Protein Binding MH - Protein Transport MH - Ras Homolog Enriched in Brain Protein/*metabolism MH - Resistance Training/*methods MH - TOR Serine-Threonine Kinases/*metabolism MH - Tuberous Sclerosis Complex 2 Protein/*metabolism MH - Young Adult PMC - PMC5504043 COIS- The authors declare that they have no competing interests. EDAT- 2017/07/12 06:00 MHDA- 2019/01/17 06:00 PMCR- 2017/07/10 CRDT- 2017/07/12 06:00 PHST- 2015/10/07 00:00 [received] PHST- 2017/06/19 00:00 [accepted] PHST- 2017/07/12 06:00 [entrez] PHST- 2017/07/12 06:00 [pubmed] PHST- 2019/01/17 06:00 [medline] PHST- 2017/07/10 00:00 [pmc-release] AID - 10.1038/s41598-017-05483-x [pii] AID - 5483 [pii] AID - 10.1038/s41598-017-05483-x [doi] PST - epublish SO - Sci Rep. 2017 Jul 10;7(1):5028. doi: 10.1038/s41598-017-05483-x.