Concerted stimuli regulating osteo-chondral differentiation from stem cells: phenotype acquisition regulated by microRNAs

被引:20
作者
Gordeladze, Jan O. [1 ,2 ,3 ]
Djouad, Farida [2 ]
Brondello, Jean-Marc [2 ]
Noel, Daniele [2 ]
Duroux-Richard, Isabelle [2 ]
Apparailly, Florence [2 ]
Jorgensen, Christian [2 ,3 ,4 ]
机构
[1] Univ Oslo, Dept Biochem, Inst Basal Med Sci, Fac Med, N-0316 Oslo, Norway
[2] INSERM, U844, Montpellier, France
[3] Univ Montpellier I, F-34006 Montpellier, France
[4] CHU Lapeyronie, Unite Immunorhumatol Therapeut, Montpellier, France
关键词
growth factors; transcription factors; mechano-stimulation; MicroRNAs; stem cells; osteoblasts; chondrocytes; tissue engineering; FOCAL ADHESION KINASE; VERTEBRATE LIMB DEVELOPMENT; ACTIVATED PROTEIN-KINASE; NITRIC-OXIDE SYNTHASE; MARROW STROMAL CELLS; KAPPA-B LIGAND; MECHANICAL STRAIN; BONE-FORMATION; SHEAR-STRESS; CHONDROCYTE DIFFERENTIATION;
D O I
10.1038/aps.2009.143
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bone and cartilage are being generated de novo through concerted actions of a plethora of signals. These act on stem cells (SCs) recruited for lineage-specific differentiation, with cellular phenotypes representing various functions throughout their life span. The signals are rendered by hormones and growth factors (GFs) and mechanical forces ensuring proper modelling and remodelling of bone and cartilage, due to indigenous and programmed metabolism in SCs, osteoblasts, chondrocytes, as well as osteoclasts and other cell types (eg T helper cells). This review focuses on the concerted action of such signals, as well as the regulatory and/or stabilizing control circuits rendered by a class of small RNAs, designated microRNAs. The impact on cell functions evoked by transcription factors (TFs) via various signalling molecules, also encompassing mechanical stimulation, will be discussed featuring microRNAs as important members of an integrative system. The present approach to cell differentiation in vitro may vastly influence cell engineering for in vivo tissue repair.
引用
收藏
页码:1369 / 1384
页数:16
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