Regulation of osteoblast differentiation mediated by BMP, Notch, and CCN3/NOV

Osteoblasts originate from common progenitors, which are capable of differentiating into other mesenchymal cell lineages such as chondrocytes, myoblasts and adipocytes. Various hormones and cytokines regulate osteoblast differentiation of mesenchymal progenitors to osteoblasts. Among these, bone mor...

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Main Authors: Akira Yamaguchi, Kei Sakamoto, Tokutarou Minamizato, Kenichi Katsube, Shoichi Nakanishi
Format: Article
Language:English
Published: Elsevier 2008-07-01
Series:Japanese Dental Science Review
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1882761608000094
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author Akira Yamaguchi
Kei Sakamoto
Tokutarou Minamizato
Kenichi Katsube
Shoichi Nakanishi
author_facet Akira Yamaguchi
Kei Sakamoto
Tokutarou Minamizato
Kenichi Katsube
Shoichi Nakanishi
author_sort Akira Yamaguchi
collection DOAJ
description Osteoblasts originate from common progenitors, which are capable of differentiating into other mesenchymal cell lineages such as chondrocytes, myoblasts and adipocytes. Various hormones and cytokines regulate osteoblast differentiation of mesenchymal progenitors to osteoblasts. Among these, bone morphogenetic proteins (BMPs) are the most potent inducers and stimulators of osteoblast differentiation: BMPs not only stimulate osteoprogenitors to differentiate into mature osteoblasts but also induce non-osteogenic cells to differentiate into osteoblast lineage cells. BMPs are important local factors that regulate Runx2, which is an essential transcription factor for osteoblast differentiation. The Notch signaling pathway is involved in a variety of cellular function, including cell proliferation, differentiation and apoptosis. Notch signaling has a dual effect on osteoblast differentiation. In terms of stimulation, functional Notch signaling is essential not only for BMP-2-induced osteoblast differentiation but also for BMP signaling itself. CCN3/NOV, a member of the CCN family of proteins, exerts inhibitory effects on BMP-2-induced osteoblast differentiation via its involvement in the BMP and Notch signaling pathways. Thus, osteoblast differentiation is critically regulated by the intimate interaction of various signaling molecules including BMP, Notch and CCN3/NOV.
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spelling doaj.art-3ce0a609e11e4c2e9a698a389ccb7b342022-12-22T00:24:01ZengElsevierJapanese Dental Science Review1882-76162008-07-01441485610.1016/j.jdsr.2007.11.003Regulation of osteoblast differentiation mediated by BMP, Notch, and CCN3/NOVAkira Yamaguchi0Kei Sakamoto1Tokutarou Minamizato2Kenichi Katsube3Shoichi Nakanishi4Section of Oral Pathology, Department of Oral Restitution, Graduate School of Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, JapanSection of Oral Pathology, Department of Oral Restitution, Graduate School of Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, JapanSection of Oral Pathology, Department of Oral Restitution, Graduate School of Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, JapanSection of Oral Pathology, Department of Oral Restitution, Graduate School of Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, JapanSection of Oral Pathology, Department of Oral Restitution, Graduate School of Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, JapanOsteoblasts originate from common progenitors, which are capable of differentiating into other mesenchymal cell lineages such as chondrocytes, myoblasts and adipocytes. Various hormones and cytokines regulate osteoblast differentiation of mesenchymal progenitors to osteoblasts. Among these, bone morphogenetic proteins (BMPs) are the most potent inducers and stimulators of osteoblast differentiation: BMPs not only stimulate osteoprogenitors to differentiate into mature osteoblasts but also induce non-osteogenic cells to differentiate into osteoblast lineage cells. BMPs are important local factors that regulate Runx2, which is an essential transcription factor for osteoblast differentiation. The Notch signaling pathway is involved in a variety of cellular function, including cell proliferation, differentiation and apoptosis. Notch signaling has a dual effect on osteoblast differentiation. In terms of stimulation, functional Notch signaling is essential not only for BMP-2-induced osteoblast differentiation but also for BMP signaling itself. CCN3/NOV, a member of the CCN family of proteins, exerts inhibitory effects on BMP-2-induced osteoblast differentiation via its involvement in the BMP and Notch signaling pathways. Thus, osteoblast differentiation is critically regulated by the intimate interaction of various signaling molecules including BMP, Notch and CCN3/NOV.http://www.sciencedirect.com/science/article/pii/S1882761608000094OsteoblastBMPNotchCCN3/NOV
spellingShingle Akira Yamaguchi
Kei Sakamoto
Tokutarou Minamizato
Kenichi Katsube
Shoichi Nakanishi
Regulation of osteoblast differentiation mediated by BMP, Notch, and CCN3/NOV
Japanese Dental Science Review
Osteoblast
BMP
Notch
CCN3/NOV
title Regulation of osteoblast differentiation mediated by BMP, Notch, and CCN3/NOV
title_full Regulation of osteoblast differentiation mediated by BMP, Notch, and CCN3/NOV
title_fullStr Regulation of osteoblast differentiation mediated by BMP, Notch, and CCN3/NOV
title_full_unstemmed Regulation of osteoblast differentiation mediated by BMP, Notch, and CCN3/NOV
title_short Regulation of osteoblast differentiation mediated by BMP, Notch, and CCN3/NOV
title_sort regulation of osteoblast differentiation mediated by bmp notch and ccn3 nov
topic Osteoblast
BMP
Notch
CCN3/NOV
url http://www.sciencedirect.com/science/article/pii/S1882761608000094
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