TGF-β2 stimulates cranial suture closure through activation of the Erk-MAPK pathway

Sang Won Lee, Kang Young Choi, Je Yoel Cho, Sung Hwa Jung, Kun Bae Song, Eui Kyun Park, Je Yong Choi, Hong In Shin, Shin Yoon Kim, Kyung Mi Woo, Jeong Hwa Baek, Soon Hyeun Nam, Young Jin Kim, Hyun Jung Kim, Hyun Mo Ryoo

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

Cranial sutures are important growth sites of the skull. During suture closure, the dura mater is one of the most important sources of various positive and negative regulatory signals. Previous results indicate that TGF-β2 from dura mater strongly accelerates suture closure, however, its exact regulatory mechanism is still unclear. In this study, we confirmed that removal of dura mater in calvarial organ culture strongly accelerates sagittal suture closure and that this effect is further enhanced by TGF-β2 treatment. TGF-β2 stimulated cell proliferation in the MC3T3-E1 cell line. Similarly, it stimulated the proliferation of cells in the sutural space in calvarial organ culture. Furthermore, TGF-β2-mediated enhanced cell proliferation and suture closure were almost completely inhibited by an Erk-MAPK blocker, PD98059. These results indicate that TGF-β2-induced activation of Erk-MAPK is an important signaling component that stimulates cell proliferation to enrich osteoprogenitor cells, thereby promoting their differentiation into osteoblasts to achieve a rapid calvarial bone expansion.

Original languageEnglish
Pages (from-to)981-991
Number of pages11
JournalJournal of Cellular Biochemistry
Volume98
Issue number4
DOIs
StatePublished - 1 Jul 2006

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