CIHR Group in Skeletal Development and Remodeling, Division of Oral Biology and Department of Physiology and Pharmacology, Schulich School of Medicine and Dentistry, University of Western Ontario, Dental Sciences Building, London, ON, N6A 5C1, Canada,
J Cell Commun Signal. 2009 Jun;3(2):89-94. doi: 10.1007/s12079-009-0037-7. Epub 2009 Jan 21.
The CCN (cyr61, ctgf, nov) family of modular proteins regulate diverse biological affects including cell adhesion, matrix production, tissue remodelling, proliferation and differentiation. Recent targeted gene disruption studies have demonstrated the CCN family to be developmentally essential for chondrogenesis, osteogenesis and angiogenesis. CCN2 is induced by agents such as angiotensin II, endothelin-1, glucocorticoids, HGF, TGFbeta, and VEGF, and by hypoxia and biomechanical and shear stress. Dysregulated expression of CCN2 has also been widely documented in many fibroproliferative diseases. This mini-review will focus on CCN2, and the recent progress in understanding CCN2 gene regulation in health and disease. That CCN2 should be considered a novel and informative surrogate clinical bio-marker for fibroproliferative disease is discussed.
CCN(cyr61、ctgf、nov)家族的模块化蛋白调节多种生物学效应,包括细胞黏附、基质生成、组织重塑、增殖和分化。最近的靶向基因敲除研究表明,CCN 家族对软骨生成、成骨和血管生成至关重要。CCN2 可被血管紧张素 II、内皮素-1、糖皮质激素、HGF、TGFβ和 VEGF 等因子诱导,也可被低氧、生物力学和切应力诱导。CCN2 的表达失调也在许多纤维增生性疾病中广泛记录。这篇综述将重点介绍 CCN2,以及最近在理解健康和疾病中 CCN2 基因调控方面的进展。讨论了 CCN2 应该被视为纤维增生性疾病的新型有价值的临床生物标志物。