| Literature DB >> 27606668 |
Ming Jiang1, Xuejie Fu1, Huilin Yang1, Fanxin Long2,3,4, Jianquan Chen1.
Abstract
mTORC1 signaling has been shown to promote limb skeletal growth through stimulation of protein synthesis in chondrocytes. However, potential roles of mTORC1 in prechondrogenic mesenchyme have not been explored. In this study, we first deleted Raptor, a unique and essential component of mTORC1, in prechondrogenic limb mesenchymal cells. Deletion of Raptor reduced the size of limb bud cells, resulting in overall diminution of the limb bud without affecting skeletal patterning. We then examined the potential role of mTORC1 in chondrogenic differentiation in vitro. Both pharmacological and genetic disruption of mTORC1 significantly suppressed the number and size of cartilage nodules in micromass cultures of limb bud mesenchymal cells. Similarly, inhibition of mTORC1 signaling in chondrogenic ATDC5 cells greatly impaired cartilage nodule formation, and decreased the expression of the master transcriptional factor Sox9, along with the cartilage matrix genes Acan and Col2a1. Thus, we have identified an important role for mTORC1 signaling in promoting limb mesenchymal cell growth and chondrogenesis during embryonic development. J. Cell. Biochem. 118: 748-753, 2017.Entities:
Keywords: CELL SIZE; CHONDROGENESIS; RAPTOR; mTORC1
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Year: 2016 PMID: 27606668 PMCID: PMC5296292 DOI: 10.1002/jcb.25728
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429