Nguyen Tri Q, Goldschmeding Roel
Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Pharm Res. 2008 Oct;25(10):2416-26. doi: 10.1007/s11095-008-9548-9. Epub 2008 Feb 12.
Renal fibrosis is the major determinant in progression of kidney disease and results from an inappropriate response to acute and chronic kidney injury. Transforming growth factor (TGF)-beta1 is the driving force behind renal fibrosis and has since long been regarded as the key factor to be targeted in prevention and treatment of renal fibrosis. Despite the impressive results obtained in experimental renal fibrosis, TGF-beta1 blockade has not yet translated into an effective and safe therapeutic in human patients. Therefore, it remains important to explore the role of additional growth factors which are involved in renal regeneration and fibrosis. Recently, bone morphogenetic protein (BMP)-7 and connective tissue growth factor (CTGF) have both emerged as novel modulators of profibrotic TGF-beta1 activity. The expression of BMP-7 is decreased in various models of renal disease, while CTGF is strongly upregulated in experimental and human renal fibrosis. In experimental kidney injury, administration of BMP-7 or inhibition of CTGF have been sufficient to result in striking improvement of renal function and structure. This review summarizes the current knowledge of BMP-7 and CTGF in the kidney, and discusses their therapeutic potential in renal fibrosis.
肾纤维化是肾脏疾病进展的主要决定因素,由对急性和慢性肾损伤的不适当反应所致。转化生长因子(TGF)-β1是肾纤维化的驱动因素,长期以来一直被视为预防和治疗肾纤维化的关键靶点。尽管在实验性肾纤维化方面取得了令人瞩目的成果,但TGF-β1阻断尚未转化为对人类患者有效且安全的治疗方法。因此,探索参与肾脏再生和纤维化的其他生长因子的作用仍然很重要。最近,骨形态发生蛋白(BMP)-7和结缔组织生长因子(CTGF)均已成为促纤维化TGF-β1活性的新型调节剂。在各种肾脏疾病模型中,BMP-7的表达降低,而CTGF在实验性和人类肾纤维化中强烈上调。在实验性肾损伤中,给予BMP-7或抑制CTGF足以显著改善肾功能和结构。本综述总结了目前关于肾脏中BMP-7和CTGF的知识,并讨论了它们在肾纤维化中的治疗潜力。