Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/99585
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Type: Journal article
Title: Brief report: The differential roles of mTORC1 and mTORC2 in mesenchymal stem cell differentiation
Author: Martin, S.
Fitter, S.
Dutta, A.
Matthews, M.
Walkley, C.
Hall, M.
Ruegg, M.
Gronthos, S.
Zannettino, A.
Citation: Stem Cells, 2015; 33(4):1359-1365
Publisher: Wiley-Blackwell
Issue Date: 2015
ISSN: 1066-5099
1549-4918
Statement of
Responsibility: 
Sally K. Martin, Stephen Fitter, Ankit K. Dutta, Mary P. Matthews,Carl R. Walkley, Michael N. Hall, Markus A. Ruegg, Stan Gronthos, Andrew C. W. Zannettino
Abstract: Adipocytes (AdCs) and osteoblasts (OBs) are derived from mesenchymal stem cells (MSCs) and differentiation toward either lineage is both mutually exclusive and transcriptionally controlled. Recent studies implicate the mammalian target of rapamycin (mTOR) pathway as important in determining MSC fate, with inhibition of mTOR promoting OB differentiation and suppressing AdC differentiation. mTOR functions within two distinct multiprotein complexes, mTORC1 and mTORC2, each of which contains the unique adaptor protein, raptor or rictor, respectively. While compounds used to study mTOR signaling, such as rapamycin and related analogs, primarily inhibit mTORC1, prolonged exposure can also disrupt mTORC2 function, confounding interpretation of inhibitor studies. As a result, the relative contribution of mTORC1 and mTORC2 to MSC fate determination remains unclear. In this study, we generated primary mouse MSCs deficient in either Rptor (RapKO) or Rictor (RicKO) using the Cre/loxP system. Cre-mediated deletion of Rptor or Rictor resulted in impaired mTORC1 and mTORC2 signaling, respectively. Under lineage-inductive culture conditions, RapKO MSCs displayed a reduced capacity to form lipid-laden AdCs and an increased capacity to form a mineralized matrix. In contrast, RicKO MSCs displayed reduced osteogenic differentiation capacity and enhanced adipogenic differentiation potential. Taken together, our findings reveal distinct roles for mTORC1 and mTORC2 in MSC lineage commitment.
Keywords: Mesenchymal stem cell; mTOR; Raptor; Rictor
Rights: © 2014 AlphaMed Press
RMID: 0030019645
DOI: 10.1002/stem.1931
Grant ID: http://purl.org/au-research/grants/nhmrc/1030528
Appears in Collections:Medicine publications

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