Department of Environmental Medicine, University of Rochester School of Medicine, Rochester, N.Y., USA.
Dig Dis. 2011;29(1):13-7. doi: 10.1159/000324123. Epub 2011 Jun 17.
The heteromeric organic solute transporter alpha-beta (Ostα-Ostβ) is expressed at relatively high levels on the basolateral membrane of enterocytes, where it plays a critical role in the intestinal absorption of bile acids and the enterohepatic circulation. However, this transporter is also expressed in nearly all human tissues, including those that are not normally thought to be involved in bile acid homeostasis, indicating that Ostα-Ostβ may have additional roles beyond bile acid transport in these other tissues, or that bile acids and their derivatives are more pervasive than currently envisioned. Emerging data from different laboratories provide support for both of these hypotheses. In particular, recent studies indicate that tissues such as brain and ovary have the capacity to synthesize bile acids or bile acid precursors. In addition, studies examining Ostα-Ostβ substrate specificity have revealed that this transporter can also accept conjugated steroids, including some neurosteroids, and that the transporter is selectively expressed in steroidogenic cells of the brain and adrenal gland, suggesting a novel function for Ostα-Ostβ. The broad tissue expression of Ostα-Ostβ is also consistent with the emerging concept that bile acids and their derivatives act as signaling molecules in diverse tissues. Bile acids activate nuclear receptors such as the farnesoid X receptor (FXR/NR1H4), the pregnane X receptor and the vitamin D receptor, are ligands for a G-protein-coupled bile acid receptor (GPBAR1/TGR5), and can also activate protein kinases A and C as well as mitogen-activated protein kinase pathways. These signaling pathways are present in many tissues and regulate processes such as triglyceride, glucose and energy homeostasis. Note that although FXR and TGR5 are thought to function primarily as bile acid receptors, they are modulated by some other sterols and select lipid metabolites, and are also widely expressed in tissues, indicating a complex interplay among diverse regulatory networks that impact critical cell and organ functions. The present report summarizes the evidence for a pleiotropic role of Ostα-Ostβ in different tissues.
异型有机溶质转运体α-β(Ostα-Ostβ)在肠上皮细胞的基底外侧膜上表达水平较高,在胆汁酸的肠吸收和肠肝循环中起着关键作用。然而,这种转运体也几乎在所有人类组织中表达,包括那些通常不被认为与胆汁酸稳态有关的组织,这表明 Ostα-Ostβ 在这些其他组织中的胆汁酸转运以外可能具有其他作用,或者胆汁酸及其衍生物比目前想象的更为普遍。来自不同实验室的新兴数据为这两种假说提供了支持。特别是,最近的研究表明,大脑和卵巢等组织具有合成胆汁酸或胆汁酸前体的能力。此外,研究 Ostα-Ostβ 底物特异性的研究表明,该转运体还可以接受结合的类固醇,包括一些神经甾体,并且该转运体在大脑和肾上腺的类固醇生成细胞中选择性表达,这表明 Ostα-Ostβ 具有新的功能。Ostα-Ostβ 的广泛组织表达也与新兴概念一致,即胆汁酸及其衍生物在不同组织中作为信号分子发挥作用。胆汁酸激活核受体,如法尼醇 X 受体(FXR/NR1H4)、孕烷 X 受体和维生素 D 受体,是 G 蛋白偶联胆汁酸受体(GPBAR1/TGR5)的配体,还可以激活蛋白激酶 A 和 C 以及丝裂原激活蛋白激酶途径。这些信号通路存在于许多组织中,并调节甘油三酯、葡萄糖和能量稳态等过程。请注意,尽管 FXR 和 TGR5 被认为主要作为胆汁酸受体发挥作用,但它们也被一些其他固醇和选择的脂质代谢物调节,并且在组织中广泛表达,表明不同调节网络之间存在复杂的相互作用,这些网络会影响关键的细胞和器官功能。本报告总结了 Ostα-Ostβ 在不同组织中具有多功能作用的证据。