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分子水平上对红细胞生成中氧感应途径和促红细胞生成素表达调控的研究进展。

Molecular Insights into the Oxygen-Sensing Pathway and Erythropoietin Expression Regulation in Erythropoiesis.

机构信息

Medical Centre for Molecular Biology, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.

Centre for Functional Genomics and Bio-Chips, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.

出版信息

Int J Mol Sci. 2021 Jun 30;22(13):7074. doi: 10.3390/ijms22137074.

Abstract

Erythropoiesis is regulated by several factors, including the oxygen-sensing pathway as the main regulator of erythropoietin (EPO) synthesis in the kidney. The release of EPO from the kidney and its binding to the EPO receptor (EPOR) on erythrocyte progenitor cells in the bone marrow results in increased erythropoiesis. Any imbalance in these homeostatic mechanisms can lead to dysregulated erythropoiesis and hematological disorders. For example, mutations in genes encoding key players of oxygen-sensing pathway and regulation of EPO production (HIF-EPO pathway), namely , , and , are well known causative factors that contribute to the development of erythrocytosis. We aimed to investigate additional molecular mechanisms involved in the HIF-EPO pathway that correlate with erythropoiesis. To this end, we conducted an extensive literature search and used several tools. We identified genes encoding transcription factors and proteins that control transcriptional activation or repression; genes encoding kinases, deacetylases, methyltransferases, conjugating enzymes, protein ligases, and proteases involved in post-translational modifications; and genes encoding nuclear transport receptors that regulate nuclear transport. All these genes may modulate the stability or activity of HIF2α and its partners in the HIF-EPO pathway, thus affecting EPO synthesis. The theoretical information we provide in this work can be a valuable tool for a better understanding of one of the most important regulatory pathways in the process of erythropoiesis. This knowledge is necessary to discover the causative factors that may contribute to the development of hematological diseases and improve current diagnostic and treatment solutions in this regard.

摘要

红细胞生成受多种因素调节,包括氧感应途径,作为肾脏中促红细胞生成素 (EPO) 合成的主要调节剂。EPO 从肾脏释放并与骨髓中红细胞祖细胞上的 EPO 受体 (EPOR) 结合,导致红细胞生成增加。这些体内平衡机制的任何失衡都可能导致红细胞生成失调和血液系统疾病。例如,编码氧感应途径和 EPO 产生调节关键因子(HIF-EPO 途径)的基因突变,即 、 、 和 ,是导致红细胞增多症发展的已知致病因素。我们旨在研究与红细胞生成相关的 HIF-EPO 途径中涉及的其他分子机制。为此,我们进行了广泛的文献检索,并使用了几种 工具。我们确定了编码转录因子和控制转录激活或抑制的蛋白质的基因;编码激酶、去乙酰化酶、甲基转移酶、结合酶、蛋白连接酶和参与翻译后修饰的蛋白酶的基因;以及编码核转运受体的基因,这些基因可调节核转运。所有这些基因都可能调节 HIF-EPO 途径中 HIF2α 及其伴侣的稳定性或活性,从而影响 EPO 的合成。我们在这项工作中提供的理论信息可以成为更好地理解红细胞生成过程中最重要的调节途径之一的有价值的工具。这一知识对于发现可能导致血液系统疾病发展的致病因素以及改善这方面的现有诊断和治疗方法是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723a/8269393/e0fb04244c14/ijms-22-07074-g001.jpg

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