4.7 Article

Activation and promotion of adipose stem cells by tumour necrosis factor-alpha preconditioning for bone regeneration

期刊

JOURNAL OF CELLULAR PHYSIOLOGY
卷 228, 期 8, 页码 1737-1744

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WILEY
DOI: 10.1002/jcp.24330

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资金

  1. Australia National Health and Medical Research Council (NHMRC)
  2. Early Career Fellowships (ECFs) [APP1036370]
  3. NHMRC [APP1036370]

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There is a major medical need for developing novel and effective approaches for repairing non-union and critical-sized bone defects. Although the mechanisms remain to be determined, it is known that inflammation plays a crucial role in initiating bone repair and regeneration. This study investigated the effect of short-term (3 days) preconditioning with tumor necrosis factor-alpha (TNF-) on proliferation, mobilization, and differentiation of adipose tissue-derived mesenchymal stem cells (ASCs). We demonstrated that TNF- pre-conditioning increased proliferation, mobilization, and osteogenic differentiation of ASCs and up-regulated bone morphogenetic protein-2 (BMP-2) protein level. BMP-2 silencing by siRNA partially inhibited osteogenic differentiation of ASCs induced by TNF-; BMP-2 pre-conditioning also significantly increased osteogenic differentiation of ASCs but the effects were significantly smaller than those observed for TNF- preconditioning. Furthermore, TNF- treatment promoted extracellular-signal-regulated kinases(Erk)1/2 and p38 mitogen-activated protein kinase (MAPK) signaling pathways, but only Erk1/2 inhibition reduced the BMP-2 levels and osteogenic differentiation induced by TNF- preconditioning. Together, these results support the hypothesis that inflammation contributes to bone regeneration by promoting proliferation, mobilization, and osteogenic differentiation of ASCs; 3 days of TNF- preconditioning, mimicking the short boost of inflammation normally occurring after bone injury, might serve as a feasible approach for directing stem cells into osteogenic differentiation. J. Cell. Physiol. 9999: XXXX, 2013. (c) 2013 Wiley Periodicals, Inc. J. Cell. Physiol. 228: 17371744, 2013. (c) 2013 Wiley Periodicals, Inc.

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