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Fate decision of mesenchymal stem cells: adipocytes or osteoblasts?

作者信息

Chen Q, Shou P, Zheng C, Jiang M, Cao G, Yang Q, Cao J, Xie N, Velletri T, Zhang X, Xu C, Zhang L, Yang H, Hou J, Wang Y, Shi Y

机构信息

The First Affiliated Hospital of Soochow University, Institutes for Translational Medicine, Soochow University, Suzhou 215006, China.

Key Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.

出版信息

Cell Death Differ. 2016 Jul;23(7):1128-39. doi: 10.1038/cdd.2015.168. Epub 2016 Feb 12.


DOI:10.1038/cdd.2015.168
PMID:26868907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4946886/
Abstract

Mesenchymal stem cells (MSCs), a non-hematopoietic stem cell population first discovered in bone marrow, are multipotent cells capable of differentiating into mature cells of several mesenchymal tissues, such as fat and bone. As common progenitor cells of adipocytes and osteoblasts, MSCs are delicately balanced for their differentiation commitment. Numerous in vitro investigations have demonstrated that fat-induction factors inhibit osteogenesis, and, conversely, bone-induction factors hinder adipogenesis. In fact, a variety of external cues contribute to the delicate balance of adipo-osteogenic differentiation of MSCs, including chemical, physical, and biological factors. These factors trigger different signaling pathways and activate various transcription factors that guide MSCs to commit to either lineage. The dysregulation of the adipo-osteogenic balance has been linked to several pathophysiologic processes, such as aging, obesity, osteopenia, osteopetrosis, and osteoporosis. Thus, the regulation of MSC differentiation has increasingly attracted great attention in recent years. Here, we review external factors and their signaling processes dictating the reciprocal regulation between adipocytes and osteoblasts during MSC differentiation and the ultimate control of the adipo-osteogenic balance.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0216/4946886/14e35c8d33ca/cdd2015168f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0216/4946886/87aa7e1bde9c/cdd2015168f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0216/4946886/5dacabd15313/cdd2015168f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0216/4946886/17f1bb221e44/cdd2015168f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0216/4946886/14e35c8d33ca/cdd2015168f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0216/4946886/87aa7e1bde9c/cdd2015168f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0216/4946886/5dacabd15313/cdd2015168f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0216/4946886/17f1bb221e44/cdd2015168f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0216/4946886/14e35c8d33ca/cdd2015168f4.jpg

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Fate decision of mesenchymal stem cells: adipocytes or osteoblasts?

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本文引用的文献

[1]
MiR-455-3p regulates early chondrogenic differentiation via inhibiting Runx2.

FEBS Lett. 2015-11-30

[2]
MicroRNA 140 Promotes Expression of Long Noncoding RNA NEAT1 in Adipogenesis.

Mol Cell Biol. 2015-10-12

[3]
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Cell. 2015-8-13

[4]
MiR-26a functions oppositely in osteogenic differentiation of BMSCs and ADSCs depending on distinct activation and roles of Wnt and BMP signaling pathway.

Cell Death Dis. 2015-8-6

[5]
Inhibition of adipogenic differentiation of human SGBS preadipocytes by androgen-regulated microRNA miR-375.

Mol Cell Endocrinol. 2015-10-15

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Hdac3 Deficiency Increases Marrow Adiposity and Induces Lipid Storage and Glucocorticoid Metabolism in Osteochondroprogenitor Cells.

J Bone Miner Res. 2016-1

[7]
miR-216a rescues dexamethasone suppression of osteogenesis, promotes osteoblast differentiation and enhances bone formation, by regulating c-Cbl-mediated PI3K/AKT pathway.

Cell Death Differ. 2015-12

[8]
Inhibition of Notch Signaling Promotes the Adipogenic Differentiation of Mesenchymal Stem Cells Through Autophagy Activation and PTEN-PI3K/AKT/mTOR Pathway.

Cell Physiol Biochem. 2015

[9]
MicroRNA-153 suppresses the osteogenic differentiation of human mesenchymal stem cells by targeting bone morphogenetic protein receptor type II.

Int J Mol Med. 2015-9

[10]
Glucose Uptake and Runx2 Synergize to Orchestrate Osteoblast Differentiation and Bone Formation.

Cell. 2015-6-18

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