| Literature DB >> 19944102 |
Shireen Kahai1, Shao-Chen Lee, Arun Seth, Burton B Yang.
Abstract
We found that nephronectin was significantly down-regulated by TGF-beta1. To determine the function of nephronectin in osteogenesis, we generated various constructs to produce stable MC3T3-E1 cell lines, expressing and secreting nephronectin protein, including full-length (Npnt), lacking EGF-like repeats (Np-MAM), and lacking RGD and MAM domains (Np-EGF). We demonstrated that nephronectin promotes differentiation during osteoblast differentiation and the EGF-like repeats were essential. Lack of these repeats resulted in inhibiting the change in morphology. Over-expression of nephronectin results in earlier formation of bone nodules than the vector control. ERK activation is essential for nephronectin-induced osteoblast differentiation.Entities:
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Year: 2010 PMID: 19944102 DOI: 10.1016/j.febslet.2009.11.077
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124