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红细胞增多症:HIF 通路的控制作用。

Erythrocytosis: the HIF pathway in control.

机构信息

Emmy Noether Research Group, Institute of Pathology, University of Technology, Dresden, Germany.

出版信息

Blood. 2013 Aug 15;122(7):1122-8. doi: 10.1182/blood-2013-01-478065. Epub 2013 Jun 3.

Abstract

Organisms living under aerobic conditions need oxygen for the metabolic conversion of nutrition into energy. With the appearance of increasingly complex animals, a specialized transport system (erythrocytes) arose during evolution to provide oxygen to virtually every single cell in the body. Moreover, in case of low environmental partial pressure of oxygen, the number of erythrocytes automatically increases to preserve sustained oxygen delivery. This process relies predominantly on the cytokine erythropoietin (Epo) and its transcription factor hypoxia inducible factor (HIF), whereas the von Hippel-Lindau (VHL) ubiquitin ligase as well as the oxygen-sensitive prolyl hydroxylases (PHDs) represent essential regulators of this oxygen-sensing system. Deregulation of particular members of this pathway (eg, PHD2, HIF2α, VHL) lead to disorders in blood homeostasis as a result of insufficient (anemia) or excessive (erythrocytosis) red blood cell production.

摘要

在有氧条件下生活的生物体需要氧气将营养物质代谢转化为能量。随着越来越复杂的动物的出现,在进化过程中出现了一种专门的运输系统(红细胞),为体内几乎每一个细胞提供氧气。此外,在环境氧分压低的情况下,红细胞数量会自动增加,以维持持续的氧气输送。这个过程主要依赖于细胞因子促红细胞生成素(Epo)及其转录因子缺氧诱导因子(HIF),而 von Hippel-Lindau(VHL)泛素连接酶以及氧敏感脯氨酰羟化酶(PHD)则是这个氧感应系统的重要调节因子。该途径中特定成员(如 PHD2、HIF2α、VHL)的失调会导致血液稳态紊乱,表现为红细胞生成不足(贫血)或过度(红细胞增多症)。

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