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Current Pharmaceutical Design

Volume 13 Issue 20
ISSN: 1381-6128
eISSN: 1873-4286


   All Titles

  Chondromodulin-I and Tenomodulin: The Negative Control of Angiogenesis in Connective Tissue
  pp.2101-2112 (12) Authors: Chisa Shukunami, Yuji Hiraki

The negative regulation of angiogenesis may provide a promising therapeutic target for a number of lifestyle-related diseases, as the switch to an angiogenic phenotype in many tissues represents a critical step during the progression of such disorders. Cartilage is avascular and shows resistance to vascular invasion from the surrounding well-vascularized mesenchyme. Using guanidine extracts of fetal bovine cartilage, we have identified and purified chondromodulin-I (ChM-I) as an angiogenesis inhibitor. The cDNA sequence of this factor has revealed that the ChM-I precursor protein is a type II transmembrane glycoprotein (334 amino acids) and that mature ChM-I is encoded in the C-terminal region of the precursor. After cleavage of the ChM-I precursor at its processing site, mature ChM-I (120 amino acids) is secreted from chondrocytes into the extracellular matrix. Following on from the identification of ChM-I as an angiogenesis inhibitor in cartilage, we have also cloned both mouse and human tenomodulin (TeM), which share significant homology with ChM-I at their C-termini. Moreover, exogenous expression experiments in COS cells suggests that TeM is a type II transmembrane glycoprotein (317 amino acids). When overexpressed in HUVECs, the C-terminal domain (116 amino acids) of the TeM protein shows both anti-angiogenic and anti-tumorigenic activities at equivalent levels to mature ChM-I. In our present review, we discuss the structure, biological activities and localization of these anti-angiogenic molecules.

  Keywords: Angiogenesis inhibitor, chondromodulin-I, tenomodulin, cartilage, tendon and ligaments, vascular invasion
  Affiliation: Institute for Frontier Medical Sciences, Kyoto University, 53 Shogoin-Kawahara-cho, Kyoto 606-850,Japan.
  Key: New Content Free Content Open Access Plus Subscribed Content

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