N-acetylcysteine stimulates osteoblastic differentiation of mouse calvarial cells

✍ Scribed by Ji Hae Jun; Sun-Hwan Lee; Han Bok Kwak; Zang Hee Lee; Sang-Beum Seo; Kyung Mi Woo; Hyun-Mo Ryoo; Gwan-Shik Kim; Jeong-Hwa Baek

• Book ID: 102301507
• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 355 KB
• Volume: 103
• Category: Article
• ISSN: 0730-2312
• DOI: 10.1002/jcb.21508

✦ Synopsis

Abstract

Estrogen deficiency causes osteoporosis via increased generation of reactive oxygen species (ROS), and thus, antioxidants may prove to be the effective therapeutic candidates. We examined the effects of the antioxidant N‐acetylcysteine (NAC) on osteoblastic differentiation in mouse calvarial cells. NAC (10–30 mM) enhanced alkaline phosphatase activity, mRNA expression of osteoblast differentiation‐associated genes and mineralized nodule formation. It also increased expression of bone morphogenetic proteins‐2, ‐4, and ‐7. The osteogenic activity of NAC was partially reduced by inhibition of glutathione synthesis. Since caffeic acid phenethyl ester did not stimulate osteoblast differentiation, it is unlikely that ROS scavenging activity of NAC is sufficient for osteogenic activity. We observed that NAC suppressed small GTPase RhoA activity and activation of RhoA by Pasteurella multocida toxin suppressed the osteogenic activity of NAC. These results suggest that NAC might exert its osteogenic activity via increased glutathione synthesis and inhibition of RhoA activation. J. Cell. Biochem. 103: 1246–1255, 2008. © 2007 Wiley‐Liss, Inc.