PDGF-induced proliferation and differentiation of synovial mesenchymal stem cells is mediated by the PI3K-PKB / Akt pathway

[Abstract] [Background] Platelet-derived growth factors (PDGFs) have been reported to enhance proliferation of synovial mesenchymal stem cells (MSCs) without reducing their multi-lineage differentiation potential in vitro. This study was aimed to elucidate the intracellular molecular pathways activa...

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Bibliographic Details
Published inJournal of Medical and Dental Sciences Vol. 65; no. 2; pp. 73 - 82
Main Authors Mari Uomizu, Takeshi Muneta, Miyoko Ojima, Ichiro Sekiya, Hideyuki Koga, Kunikazu Tsuji
Format Journal Article
LanguageEnglish
Published Tokyo Medical and Dental University 2018
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ISSN1342-8810
DOI10.11480/jmds.650204

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Summary:[Abstract] [Background] Platelet-derived growth factors (PDGFs) have been reported to enhance proliferation of synovial mesenchymal stem cells (MSCs) without reducing their multi-lineage differentiation potential in vitro. This study was aimed to elucidate the intracellular molecular pathways activated by PDGFs. [Methods] Synovial MSCs were isolated from patients who underwent total knee arthroplasty with institutional approval and patients' permission. Cell proliferation and differentiation assays were performed in the presence of small inhibitor molecules specific for intracellular kinases. [Results] Both PDGF-AA and -BB enhanced cell proliferation in medium containing reduced serum. These effects were significantly reduced by a phosphatidylinositol- 3 kinase (PI3K) inhibitor, LY290042. During chondrogenic spheroid formation in vitro, LY290042 significantly reduced the size of spheroids enhanced by PDGF-AA. LY290042 also significantly inhibited in vitro chondrogenic and osteoblastic differentiation of synovial MSCs. [Conclusion] Our data indicated that activation of the PI3K-PKB/Akt pathway by PDGFs plays an important role in both proliferation and differentiation of synovial MSCs. Hence, these data could be beneficial for optimizing the in vitro culture conditions of synovial MSCs for clinical use.
ISSN:1342-8810
DOI:10.11480/jmds.650204