Wisplinghoff Medical Laboratories, Cologne, Germany.
Vitam Horm. 2011;85:59-77. doi: 10.1016/B978-0-12-385961-7.00004-4.
While autocrine stimulation of cells by Activin A and/or its family member transforming growth factor β (TGF-β) is a phenomenon observed in a variety of cell types, little is known of putative intracellular signaling loops of these cytokines. Intracellular actions of several peptide hormones, growth factors, as well as of extracellular signaling enzymes and DNA-binding proteins, either within target cells or within their cells of synthesis have been shown. Although these intracrine moieties are structurally diverse, they share certain characteristics of synthesis and function. Depending on the cell type, there are reports of stimulatory as well as inhibitory mechanisms induced by such intracrine mechanisms, and this also accounts for transforming growth factor β (TGF-β), whereas only stimulatory intracrine signaling of Activin A could be demonstrated so far. Stimulatory intracrine signaling loops of TGF-β were shown following calpain-dependent intracellular proteolytic activation of the latent cytokine in hepatocytes under cellular stress conditions of this cytokine, leading to transcriptional activation of connective tissue growth factor (CTGF/CCN2) as a representative TGF-β-sensitive reporter gene. In contrast to TGF-β, increasing intrahepatocellular concentrations of Activin A are not the result of release from an intracellularly deposited latent complex, but of active de novo synthesis. The stimulatory intracrine signaling pathways of both, TGF-β and Activin A, are proposed to occur via Alk4/Alk5 receptors and Smad2, whereas additional activation of Smad3 only seems to be involved in intracrine Activin A signaling. However, intracrine TGF-β signaling may itself also be inhibitory as active TGF-β is also able to bind to intracellular TGF-β type II receptor, resulting in a ligand-induced impediment in receptor trafficking to the cell surface. Whether stimulatory or inhibitory modulation of the TGF-β pathway takes place seems to depend on the cell type and environmental conditions. Future studies are necessary at this point.
虽然激活素 A 和/或其家族成员转化生长因子 β(TGF-β)对细胞的自分泌刺激是各种细胞类型中观察到的现象,但对于这些细胞因子的假定细胞内信号转导环知之甚少。已经表明,几种肽激素、生长因子以及细胞外信号酶和 DNA 结合蛋白在靶细胞内或其合成细胞内具有细胞内作用。尽管这些内原性物质在结构上是多种多样的,但它们具有某些合成和功能的特征。根据细胞类型,有报道称这种内原性机制诱导刺激和抑制机制,这也适用于转化生长因子 β(TGF-β),而迄今为止仅证明了激活素 A 的刺激内原性信号传导。在这种细胞因子的细胞应激条件下,肝细胞中潜在细胞因子的钙蛋白酶依赖性细胞内蛋白水解激活显示 TGF-β 的刺激内原性信号转导,导致结缔组织生长因子(CTGF/CCN2)作为代表性 TGF-β 敏感报告基因的转录激活。与 TGF-β 相反,肝内激活素 A 浓度的增加不是由于从细胞内沉积的潜伏复合物中释放出来,而是由于主动从头合成。两种内原性信号通路 TGF-β 和 Activin A 均被提议通过 Alk4/Alk5 受体和 Smad2 发生,而 Smad3 的额外激活似乎仅参与内原性 Activin A 信号传导。然而,内原性 TGF-β 信号传导本身也可能是抑制性的,因为活性 TGF-β也能够与细胞内 TGF-β 型 II 受体结合,导致配体诱导的受体向细胞表面的运输受阻。内源性 TGF-β 途径是刺激还是抑制性调节似乎取决于细胞类型和环境条件。在这一点上,未来的研究是必要的。