Journal
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume 345, Issue 3, Pages 1224-1231Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2006.05.045
Keywords
bone morphogenetic proteins; serum; myogenesis; osteoblasts; liquid chromatography-tandem mass spectrometry
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Myogenic differentiation is suppressed in vitro by unknown factors present in fetal bovine serum (FBS). We found that specific inhibitors of bone morphogenetic proteins (BMPs) stimulated myogenic differentiation even in the presence of 20% FBS, which in turn activated specific BMP signaling. Moreover, these specific BMP inhibitors blocked maturation of osteoblastic cells induced by FBS, indicating that BMP-like factor(s) in serum regulate both myogenic and osteoblastic differentiation. The factor identified had an apparent molecular weight (Mw) of over 100 kDa on a Superdex 200 column for molecular sieving HPLC, but an apparent Mw of 3 3 kDa on SDS-PAGE under non-reducing conditions. Analysis of a purified preparation from FBS (5 L) by liquid chromatography-tandem mass spectrometry revealed the presence of an amino acid sequence conserved between mature human and murine BMP-4. This is the first study to show that BMP-4 is present in FBS as a large complex. (c) 2006 Elsevier Inc. All rights reserved.
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