Novel mode of processing and secretion of connective tissue growth factor/ecogenin (CTGF/Hcs24) in chondrocytic HCS-2/8 cells

被引:32
作者
Kubota, S
Eguchi, T
Shimo, T
Nishida, T
Hattori, T
Kondo, S
Nakanishi, T
Takigawa, M
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Biochem & Mol Dent, Sch Dent, Okayama 7008525, Japan
[2] Okayama Univ, Biodent Res Ctr, Sch Dent, Okayama 7008525, Japan
基金
日本学术振兴会;
关键词
connective tissue growth factor (CTGF); chondrocyte; cartilage; HCS-2/8; extracellular matrix (ECM);
D O I
10.1016/S8756-3282(01)00492-6
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The synthesis, processing, and secretion of human connective tissue growth factor (CTGF/Hcs24) in a human chondrocytic cell line, HCS-2/8, were analyzed immunochemically. By metabolic pulse-labeling, chasing, and subsequent immunoprecipitation analyses, active synthesis of CTGF was observed not only in growing HCS-2/8 cells, but also in confluent cells. However, secretion and processing of CTGF were found to be regulated differentially, depending upon the growth status. During phases of growth, HCS-2/8 cells released CTGF molecules immediately without sequestering them within the cell layer. In contrast, after the cells reached confluence, the secretion slowed, resulting in an accumulation of CTGF in the cells or extracellular matrices (ECMs). Also, in confluent cell layers, a 10 kDa protein that was reactive to an anti-CTGF serum was observed. This CTGF-related small protein was not detected immediately after labeling, but gradually appeared within 6 h after chase, which suggests its entity as a processed subfragment of CTGF. Surprisingly, the 10 kDa protein was stable even 48 h after synthesis, and was not released by ECM digestion, suggesting an intracellular maintenance and function. Taken together, the behavior of CTGF in HCS-2/8 cells is remarkably different from that reported in fibroblasts, which may represent unique roles for CTGF in the growth and differentiation of chondrocytes. (C) 2001 by Elsevier Science Inc. All rights reserved.
引用
收藏
页码:155 / 161
页数:7
相关论文
共 37 条
[1]
ADACHI Y, 1992, J BIOL CHEM, V267, P21977
[2]
Enhanced insulin-like growth factor finding protein-related protein 2 (connective tissue growth factor) expression in patients with idiopathic pulmonary fibrosis and pulmonary sarcoidosis [J].
Allen, JT ;
Knight, RA ;
Bloor, CA ;
Spiteri, MA .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 21 (06) :693-700
[3]
THE MODULAR ARCHITECTURE OF A NEW FAMILY OF GROWTH-REGULATORS RELATED TO CONNECTIVE-TISSUE GROWTH-FACTOR [J].
BORK, P .
FEBS LETTERS, 1993, 327 (02) :125-130
[4]
CONNECTIVE-TISSUE GROWTH-FACTOR - A CYSTEINE-RICH MITOGEN SECRETED BY HUMAN VASCULAR ENDOTHELIAL-CELLS IS RELATED TO THE SRC-INDUCED IMMEDIATE EARLY GENE-PRODUCT CEF-10 [J].
BRADHAM, DM ;
IGARASHI, A ;
POTTER, RL ;
GROTENDORST, GR .
JOURNAL OF CELL BIOLOGY, 1991, 114 (06) :1285-1294
[6]
Dexamethasone is a novel potent inducer of connective tissue growth factor expression - Implications for glucocorticoid therapy [J].
Dammeier, J ;
Beer, HD ;
Brauchle, M ;
Werner, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (29) :18185-18190
[7]
Grotendorst Gary R., 1997, Cytokine and Growth Factor Reviews, V8, P171, DOI 10.1016/S1359-6101(97)00010-5
[8]
Grotendorst GR, 1996, CELL GROWTH DIFFER, V7, P469
[9]
Expression of the Elm1 gene, a novel gene of the CCN (connective tissue growth factor, Cyr61/Cef10, and neuroblastoma overexpressed gene) family, suppresses in vivo tumor growth and metastasis of K-1735 murine melanoma cells [J].
Hashimoto, Y ;
Shindo-Okada, N ;
Tani, M ;
Nagamachi, Y ;
Takeuchi, K ;
Shiroishi, T ;
Toma, H ;
Yokota, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (03) :289-296
[10]
Isolation and characterization of a rheumatoid arthritis-specific antigen (RA-A47) from a human chondrocytic cell line (HCS-2/8) [J].
Hattori, T ;
Fujisawa, T ;
Sasaki, K ;
Yutani, Y ;
Nakanishi, T ;
Takahashi, K ;
Takigawa, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 245 (03) :679-683