Literature DB >> 14611685

Novel enzyme-linked immunosorbent assay systems for the quantitative analysis of connective tissue growth factor (CTGF/Hcs24/CCN2): detection of HTLV-I tax-induced CTGF from a human carcinoma cell line.

Harumi Kawaki1, Satoshi Kubota, Masanao Minato, Norifumi H Moritani, Takako Hattori, Hiroshi Hanagata, Mamoru Kubota, Akira Miyauchi, Tohru Nakanishi, Masaharu Takigawa.   

Abstract

Connective tissue growth factor/hypertrophic chondrocyte-specific gene product 24 (CTGF/Hcs24/CCN2) is known as a multifunctional growth factor. It stimulates proliferation, migration, and extracellular matrix production of mesenchymal cells, and is highly expressed in hypertrophic chondrocytes. In this study, we constructed useful ELISA systems for the analysis of CTGF and its modular fragments. For this objective we prepared four different antihuman CTGF monoclonal antibodies. One, specific for the VWC module, was utilized as the detecting antibody, and the other three, recognizing CT, IGFBP, and VWC modules, respectively, were employed as capture antibodies. Then we established three novel quantitative analysis systems for CTGF. The first system recognizing CT and VWC modules was useful to measure full-length CTGF with improved sensitivity. Utilizing this system, we found significant enhancement of CTGF production from a human carcinoma cell line transduced by HTLV-I tax gene, where the finding indicates the possible involvement of Tax in carcinogenesis. The second system, seeing IGFBP and VWC modules, could quantify not only CTGF, but also may be useful to analyze processed N-terminal fragments. The third system, utilizing capture and detection antibodies against the VWC module, was able to quantify the VWC module only, while it did not recognize full-length CTGF. Since CTGF is actually processed into subfragments, and functional assignment of each module is of interest, these systems are expected to contribute to the progress of CTGF investigations.

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Year:  2003        PMID: 14611685     DOI: 10.1089/104454903770238111

Source DB:  PubMed          Journal:  DNA Cell Biol        ISSN: 1044-5498            Impact factor:   3.311


  3 in total

1.  Association of the metastatic phenotype with CCN family members among breast and oral cancer cells.

Authors:  Toshihiro Ohgawara; Satoshi Kubota; Harumi Kawaki; Naito Kurio; Tarek Abd El Kader; Mitsuhiro Hoshijima; Danilo Janune; Tsuyoshi Shimo; Bernard Perbal; Akira Sasaki; Masaharu Takigawa
Journal:  J Cell Commun Signal       Date:  2011-04-18       Impact factor: 5.782

2.  Cooperative regulation of chondrocyte differentiation by CCN2 and CCN3 shown by a comprehensive analysis of the CCN family proteins in cartilage.

Authors:  Harumi Kawaki; Satoshi Kubota; Akiko Suzuki; Noureddine Lazar; Tomohiro Yamada; Tatsushi Matsumura; Toshihiro Ohgawara; Takeyasu Maeda; Bernard Perbal; Karen M Lyons; Masaharu Takigawa
Journal:  J Bone Miner Res       Date:  2008-11       Impact factor: 6.741

3.  Potential cellular conformations of the CCN3(NOV) protein.

Authors:  Stanimir Kyurkchiev; Herman Yeger; Anne - Marie Bleau; Bernard Perbal
Journal:  Cell Commun Signal       Date:  2004-09-10       Impact factor: 5.712

  3 in total

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