转化生长因子β:抗狭窄治疗的一个有希望的靶点

J. Chamberlain
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引用次数: 17

摘要

转化生长因子- β (tgf - β)是一类细胞因子的总称,它们对生长发育的许多方面都有广泛的影响。tgf - β亚型由大多数细胞类型产生,并通过与细胞表面不同受体的相互作用,以上下文依赖的自分泌、旁分泌或内分泌方式发挥广泛的作用。tgf - β参与伤口愈合过程,因此在经皮冠状动脉腔内成形术(PTCA)或支架植入术后再狭窄病变的形成中起重要作用。也许是因为其广泛的影响,tgf - β通常以潜伏的形式从细胞中释放出来,它的激活和信号传导是复杂的。在动物模型中,通过抑制tgf - β 1、tgf - β 2和tgf - β 3异构体的表达、激活或信号传导,可以减少疤痕和纤维化。然而,迄今为止,很少有临床试验。本文综述了目前关于tgf - β的激活和信号传导的知识,并重点介绍了抗tgf - β策略,这些策略可能会导致PTCA或支架置入后再狭窄的预防临床应用。
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Transforming Growth Factor‐β:A Promising Target for Anti‐Stenosis Therapy
Transforming growth factor-beta (TGF-beta) is the general name for a family of cytokines which have widespread effects on many aspects of growth and development. The TGF-beta isoforms are produced by most cell types and exert a wide range of effects in a context-dependent autocrine, paracrine or endocrine fashion via interactions with distinct receptors on the cell surface. TGF-beta is involved in the wound healing process and, thus plays a significant role in the formation of a restenotic lesion after percutaneous transluminal coronary angioplasty (PTCA) or stenting. Perhaps because of its wide-ranging effects, TGF-beta is usually released from cells in a latent form, and its activation and signaling are complex. Manipulation of the TGF-beta1, TGF-beta2, and TGF-beta3 isoforms by inhibiting their expression, activation, or signaling reduces scarring and fibrosis in animal models. However, to date, few have reached clinical trial. This review summarizes current knowledge on the activation and signaling of TGF-beta, and focuses on the anti-TGF-beta strategies which may lead to clinical applications in the prevention of restenosis following PTCA or stenting.
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