Evidence map›Paper›PMID 28971834›Full record

ArticleAmerican journal of physiology. Cell physiology2017

Differential localization and anabolic responsiveness of mTOR complexes in human skeletal muscle in response to feeding and exercise.

Nathan Hodson, Chris McGlory, Sara Y Oikawa, Stewart Jeromson, Zhe Song, Markus A Rüegg, D Lee Hamilton, Stuart M Phillips, Andrew Philp

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 52 citations in OpenAlex.

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  12. Cardamonin inhibits cell proliferation by caspase-mediated cleavage of Raptor.Naunyn-Schmiedeberg's archives of pharmacology · 2021
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  15. Muscle follistatin gene delivery increases muscle protein synthesis independent of periodical physical inactivity and fasting.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Nathan HodsonSchool of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, United Kingdom.
Chris McGloryDepartment of Kinesiology, McMaster University, Hamilton, Ontario, Canada.
Sara Y OikawaDepartment of Kinesiology, McMaster University, Hamilton, Ontario, Canada.
Stewart JeromsonFaculty of Health Sciences and Sport, University of Stirling, Stirling, United Kingdom; and.
Zhe SongSchool of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, United Kingdom.
Markus A RüeggBiozentrum, University of Basel, Basel, Switzerland.
D Lee HamiltonFaculty of Health Sciences and Sport, University of Stirling, Stirling, United Kingdom; and.
Stuart M PhillipsDepartment of Kinesiology, McMaster University, Hamilton, Ontario, Canada.
Andrew PhilpSchool of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, United Kingdom; a.philp@bham.ac.uk.ORCID http://orcid.org/0000-0003-3860-4136
McMaster University · CAUniversity of Birmingham · GBUniversity of Stirling · GBUniversity of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanistic target of rapamycin (mTOR) resides as two complexes within skeletal muscle. mTOR complex 1 [mTORC1-regulatory associated protein of mTOR (Raptor) positive] regulates skeletal muscle growth, whereas mTORC2 [rapamycin-insensitive companion of mTOR (Rictor) positive] regulates insulin sensitivity. To examine the regulation of these complexes in human skeletal muscle, we utilized immunohistochemical analysis to study the localization of mTOR complexes before and following protein-carbohydrate feeding (FED) and resistance exercise plus protein-carbohydrate feeding (EXFED) in a unilateral exercise model. In basal samples, mTOR and the lysosomal marker lysosomal associated membrane protein 2 (LAMP2) were highly colocalized and remained so throughout. In the FED and EXFED states, mTOR/LAMP2 complexes were redistributed to the cell periphery [wheat germ agglutinin (WGA)-positive staining] (time effect;

Indexed as

EatingEnergy MetabolismExerciseAdultDietary CarbohydratesDietary ProteinsHumansLysosomal-Associated Membrane Protein 2LysosomesMaleMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Muscle ContractionProtein TransportProto-Oncogene Proteins c-aktQuadriceps MuscleDietary CarbohydratesDietary ProteinsLAMP2 protein, humanLysosomal-Associated Membrane Protein 2Mechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Proto-Oncogene Proteins c-aktRapamycin-Insensitive Companion of mTOR ProteinRegulatory-Associated Protein of mTORribosomal protein S6 kinase, 70kD, polypeptide 1Ribosomal Protein S6 Kinases, 70-kDaRICTOR protein, humanRPTOR protein, humanlysosomemTORC1mTORC2RaptorRictor

Identifiers

PMID28971834
PMCPMC5814591
OpenAlexW2758796129

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.