Esposito C, Fasoli G, Rampino T, Dal Canton A
Unità Operativa di Nefrologia, Dialisi e Trapianto, IRCCS Policlinico San Matteo, Università di Pavia, Pavia.
G Ital Nefrol. 2006 Jul-Aug;23(4):381-8.
HGF is a multifunctional polypeptide with mitogenic, motogenic and morphogenic effects. These effects are mediated by c-met, a specific receptor of HGF and a member of the receptor tyrosine kinase superfamily, virtually expressed in every type of kidney cell. HGF has a central role during embryogenesis since it stimulates epithelial differentiation of metanephric mesenchymal cells and induces branching tubules, as experiments in epithelial cells cultures demonstrated. Several studies have shown also that HGF accelerates the recovery from toxic-ischemic acute renal failure. This effect seems to be mediated by the inhibition of programmed cell death and an increased cell survival. HGF inhibits apoptosis by upregulating the protooncogene Bcl-2 and downregulating Bax. Since HGF can modulate extracellular matrix turnover, authors suggest its beneficial role in tissue remodelling and particularly in chronic renal diseases. Several studies reported a key role for HGF in reducing interstitial fibrosis and glomerular sclerosis, both in in vivo and in vitro models. This protective effect is secondary to HGF antagonizing the profibrotic action of TGF-beta. HGF modulates the balance between synthesis and degradation of extracellular matrix, increasing the expression of metalloproteases and reducing the production of their specific inhibitors TIMPs. Furthermore HGF suppresses the effect of TGF-beta by blocking the axis TGF-beta/Smad. Last, the antifibrotic effect of HGF might be modulated by the proliferative status of target cells. To sum up, the supplementation of exogenous HGF or the induction of endogenous HGF expression may provide an effective therapeutic strategy for combating chronic renal diseases.
肝细胞生长因子(HGF)是一种具有促有丝分裂、促运动和促形态发生作用的多功能多肽。这些作用由c-met介导,c-met是HGF的特异性受体,属于受体酪氨酸激酶超家族成员,几乎在每种类型的肾细胞中都有表达。正如上皮细胞培养实验所证明的,HGF在胚胎发生过程中起核心作用,因为它刺激后肾间充质细胞的上皮分化并诱导肾小管分支。多项研究还表明,HGF能加速中毒性缺血性急性肾衰竭的恢复。这种作用似乎是通过抑制程序性细胞死亡和增加细胞存活来介导的。HGF通过上调原癌基因Bcl-2和下调Bax来抑制细胞凋亡。由于HGF可以调节细胞外基质的周转,作者认为其在组织重塑尤其是慢性肾脏疾病中具有有益作用。多项研究报道,在体内和体外模型中,HGF在减少间质纤维化和肾小球硬化方面起关键作用。这种保护作用是由于HGF拮抗转化生长因子-β(TGF-β)的促纤维化作用。HGF调节细胞外基质合成与降解之间的平衡,增加金属蛋白酶的表达并减少其特异性抑制剂金属蛋白酶组织抑制因子(TIMPs)的产生。此外,HGF通过阻断TGF-β/Smad轴来抑制TGF-β的作用。最后,HGF的抗纤维化作用可能受靶细胞增殖状态的调节。综上所述,补充外源性HGF或诱导内源性HGF表达可能为对抗慢性肾脏疾病提供一种有效的治疗策略。