Induction of bone matrix protein expression by native bone matrix proteins in C2C12 culture.
- Author:
Zhen-Ming HU
1
;
Sean A F PEEL
;
Stephen K C HO
;
George K B SANDOR
;
Cameron M L CLOKIE
Author Information
- Publication Type:Journal Article
- MeSH: Alkaline Phosphatase; metabolism; Animals; Bone Matrix; metabolism; Bone Morphogenetic Proteins; pharmacology; Cattle; Cell Line; DNA; metabolism; Gene Expression Regulation; physiology; Mice; Osteoblasts; drug effects; metabolism
- From: Biomedical and Environmental Sciences 2009;22(2):164-169
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo study the expression of bone matrix protein (BMP) induced by bovine bone morphogenetic proteins (BMPs) in vitro.
METHODSType I collagen, osteopontin (OPN), osteonectin (ON), osteocalcin (OC), and bone sialoprotein (BSP) were detected by immunohistochemistry in C2C12 cultured from day 1 to day 28.
RESULTSThe signaling of bone matrix protein expression became weaker except for type I collagen, OC and BSP after 5 days. Fourteen days after culture, the positive signaling of type I collagen, OPN, ON, OC, and BSP was gradually declined, and could be detected significantly as compared with that of the negative control on day 28. BMP assay showed that the alkaline phosphatase (ALP) activity was higher in C2C12 culture than in the control during the 14-day culture. Also, total protein and DNA significantly increased during the 14-day culture. High levels of ALP were seen in preosteoblasts and osteoblasts in vivo and in differentiating osteoblasts in vitro. ALP was well recognized as a marker reflecting osteoblastic activity.
CONCLUSIONNative bovine BMP induces conversion of myoblasts into osteoblasts, produces type I collagen, and plays significantly role in osteoinduction and bone matrix mineralization of C2C12 in vitro.
