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Effects of CTGF/Hcs24, a hypertrophic chondrocyte‐specific gene product, on the proliferation and differentiation of osteoblastic cells in vitro
Author(s) -
Nishida Takashi,
Nakanishi Tohru,
Asano Masahiro,
Shimo Tsuyoshi,
Takigawa Masaharu
Publication year - 2000
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/1097-4652(200008)184:2<197::aid-jcp7>3.0.co;2-r
Subject(s) - ctgf , endochondral ossification , osteocalcin , growth factor , chondrocyte , osteoblast , alkaline phosphatase , chemistry , microbiology and biotechnology , cellular differentiation , cell culture , biology , medicine , receptor , endocrinology , in vitro , cartilage , biochemistry , gene , anatomy , genetics , enzyme
Connective tissue growth factor/hypertrophic chondrocyte‐specific gene product Hcs24 (CTGF/Hcs24) promotes the proliferation and differentiation of chondrocytes and endothelial cells which are involved in endochondral ossification (Shimo et al., 1998, J Biochem 124:130–140; Shimo et al., 1999, J Biochem 126:137–145; Nakanishi et al., 2000, Endocrinology 141:264–273). To further clarify the role of CTGF/Hcs24 in endochondral ossification, here we investigated the effects of CTGF/Hcs24 on the proliferation and differentiation of osteoblastic cell lines in vitro. A binding study using 125 I‐labeled recombinant CTGF/Hcs24 (rCTGF/Hcs24) disclosed two classes of specific binding sites on a human osteosarcoma cell line, Saos‐2. The apparent dissociation constant (Kd) value of each binding site was 17.2 and 391 nM, respectively. A cross‐linking study revealed the formation of 125 I‐rCTGF/Hcs24‐receptor complex with an apparent molecular weight of 280 kDa. The intensity of 125 I‐rCTGF/Hcs24‐receptor complex decreased on the addition of increasing concentrations of unlabeled rCTGF/Hcs24, but not platelet‐derived growth factor‐BB homodimer or basic fibroblast growth factor. These findings suggest that osteoblastic cells have specific receptor molecules for CTGF/Hcs24. rCTGF/Hcs24 promoted the proliferation of Saos‐2 cells and a mouse osteoblast cell line MC3T3‐E1 in a dose‐ and time‐dependent manner. rCTGF/Hcs24 also increased mRNA expression of type I collagen, alkaline phosphatase, osteopontin, and osteocalcin in both Saos‐2 cells and MC3T3‐E1 cells. Moreover, rCTGF/Hcs24 increased alkaline phosphatase activity in both cells. It also stimulated collagen synthesis in MC3T3‐E1 cells. Furthermore, rCTGF/Hcs24 stimulated the matrix mineralization on MC3T3‐E1 cells and its stimulatory effect was comparable to that of bone morphogenetic protein‐2. These findings indicate that CTGF/Hcs24 is a novel, potent stimulator for the proliferation and differentiation of osteoblasts in addition to chondrocytes and endothelial cells. Because of these functions, we are re‐defining CTGF/Hcs24 as a major factor to promote endochondral ossification to be called “ecogenin: endochondral ossification genetic factor.” J. Cell. Physiol. 184:197–206, 2000. © 2000 Wiley‐Liss, Inc.