• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

促红细胞生成素与红细胞生成的发育调控

Developmental regulation of erythropoietin and erythropoiesis.

作者信息

Moritz K M, Lim G B, Wintour E M

机构信息

Howard Florey Institute of Experimental Physiology and Medicine, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Am J Physiol. 1997 Dec;273(6):R1829-44. doi: 10.1152/ajpregu.1997.273.6.R1829.

DOI:10.1152/ajpregu.1997.273.6.R1829
PMID:9435635
Abstract

It is well established that erythropoiesis occurs first in the yolk sac, then in the liver, subsequently moving to the bone marrow and, in rodents, the spleen during development. The origin of the erythropoietic precursors and some factors suggested to be important for the changing location of erythropoiesis are discussed in this review. Until recently, the major site of erythropoietin (Epo) production in the fetus was thought to be the liver, but studies have shown now that the Epo gene is expressed strongly in the fetal kidney, even in the temporary mesonephros. The metanephric Epo mRNA is upregulated by anemia, downregulated by glucocorticoids, and contributes substantially to circulating hormone levels in hemorrhaged ovine fetuses. Other sites of Epo and Epo receptor production, likely to have important actions during development, are the placenta and the brain.

摘要

众所周知,红细胞生成首先发生在卵黄囊,然后在肝脏,随后转移至骨髓,在啮齿动物发育过程中还会转移至脾脏。本文综述了红细胞生成前体的起源以及一些被认为对红细胞生成位置变化很重要的因素。直到最近,胎儿中促红细胞生成素(Epo)的主要产生部位被认为是肝脏,但现在研究表明,Epo基因在胎儿肾脏中强烈表达,即使在临时性中肾也是如此。后肾Epo mRNA受贫血上调,受糖皮质激素下调,并且对失血绵羊胎儿的循环激素水平有很大贡献。Epo和Epo受体产生的其他部位,可能在发育过程中具有重要作用,是胎盘和大脑。

相似文献

1
Developmental regulation of erythropoietin and erythropoiesis.促红细胞生成素与红细胞生成的发育调控
Am J Physiol. 1997 Dec;273(6):R1829-44. doi: 10.1152/ajpregu.1997.273.6.R1829.
2
Pleiotropic functions of erythropoietin.促红细胞生成素的多效性功能。
Intern Med. 2003 Feb;42(2):142-9. doi: 10.2169/internalmedicine.42.142.
3
Erythropoietin (Epo) and EpoR expression and 2 waves of erythropoiesis.促红细胞生成素(Epo)和促红细胞生成素受体(EpoR)的表达与两波红细胞生成
Blood. 2001 Sep 1;98(5):1408-15. doi: 10.1182/blood.v98.5.1408.
4
A developmental transition in definitive erythropoiesis: erythropoietin expression is sequentially regulated by retinoic acid receptors and HNF4.确定型红细胞生成中的发育转变:促红细胞生成素的表达受视黄酸受体和肝细胞核因子4的顺序调控。
Genes Dev. 2001 Apr 1;15(7):889-901. doi: 10.1101/gad.871601.
5
Erythropoietin production in neuroepithelial and neural crest cells during primitive erythropoiesis.神经上皮细胞和神经嵴细胞在原始红细胞生成过程中的促红细胞生成素生成。
Nat Commun. 2013;4:2902. doi: 10.1038/ncomms3902.
6
Mammalian homeobox B6 expression can be correlated with erythropoietin production sites and erythropoiesis during development, but not with hematopoietic or nonhematopoietic stem cell populations.哺乳动物同源盒B6的表达在发育过程中可能与促红细胞生成素的产生部位及红细胞生成相关,但与造血或非造血干细胞群体无关。
Blood. 1997 Apr 15;89(8):2723-35.
7
Quantitation of the mRNA levels of Epo and EpoR in various tissues in the ovine fetus.绵羊胎儿各组织中促红细胞生成素(Epo)和促红细胞生成素受体(EpoR)mRNA水平的定量分析。
Mol Cell Endocrinol. 2002 Feb 25;188(1-2):207-18. doi: 10.1016/s0303-7207(01)00718-3.
8
Erythropoietin mRNA expression in human fetal and neonatal tissue.人胎儿及新生儿组织中促红细胞生成素mRNA的表达
Blood. 1998 Nov 1;92(9):3218-25.
9
Erythropoietin and hypoxia inducible factor-1 expression in the mid-trimester human fetus.
Acta Paediatr Suppl. 2002;91(438):27-30. doi: 10.1111/j.1651-2227.2002.tb02902.x.
10
Erythropoietin gene expression: developmental-stage specificity, cell-type specificity, and hypoxia inducibility.促红细胞生成素基因表达:发育阶段特异性、细胞类型特异性及低氧诱导性。
Tohoku J Exp Med. 2015 Mar;235(3):233-40. doi: 10.1620/tjem.235.233.

引用本文的文献

1
Oxidative stress and senescence in aging kidneys: the protective role of SIRT1.衰老肾脏中的氧化应激与衰老:SIRT1的保护作用
EXCLI J. 2024 Aug 27;23:1030-1067. doi: 10.17179/excli2024-7519. eCollection 2024.
2
Vitamin C-Dependent Uptake of Non-Heme Iron by Enterocytes, Its Impact on Erythropoiesis and Redox Capacity of Human Erythrocytes.肠细胞对非血红素铁的维生素C依赖性摄取及其对人体红细胞生成和氧化还原能力的影响。
Antioxidants (Basel). 2024 Aug 9;13(8):968. doi: 10.3390/antiox13080968.
3
Monitoring methaemoglobinaemia in birds using 5 μL of whole blood.
使用 5μL 全血监测鸟类的高铁血红蛋白血症。
PLoS One. 2023 Mar 16;18(3):e0282820. doi: 10.1371/journal.pone.0282820. eCollection 2023.
4
Automated analysis of mitochondrial dimensions in mesenchymal stem cells: Current methods and future perspectives.间充质干细胞中线粒体尺寸的自动化分析:当前方法与未来展望
Heliyon. 2023 Jan 18;9(1):e12987. doi: 10.1016/j.heliyon.2023.e12987. eCollection 2023 Jan.
5
Cellular composition of the black scorpionfish (Scorpaena porcus, L 1758) blood and head kidney under short-time acute exposure to hypoxia.短时间急性缺氧暴露下黑鮟鱇(Scorpaena porcus,L 1758)血液和头肾的细胞组成。
Fish Physiol Biochem. 2022 Oct;48(5):1209-1220. doi: 10.1007/s10695-022-01115-y. Epub 2022 Aug 16.
6
Late-Pregnancy Fetal Hypoxia Is Associated With Altered Glucose Metabolism and Adiposity in Young Adult Offspring of Women With Type 1 Diabetes.妊娠晚期胎儿缺氧与 1 型糖尿病女性子代成年早期葡萄糖代谢和肥胖改变有关。
Front Endocrinol (Lausanne). 2021 Oct 27;12:738570. doi: 10.3389/fendo.2021.738570. eCollection 2021.
7
The Effect of Size, Maturation, Global Asphyxia, Cerebral Ischemia, and Therapeutic Hypothermia on the Pharmacokinetics of High-Dose Recombinant Erythropoietin in Fetal Sheep.大小、成熟度、全身缺氧、脑缺血和治疗性低温对胎儿羊高剂量重组红细胞生成素药代动力学的影响。
Int J Mol Sci. 2020 Apr 25;21(9):3042. doi: 10.3390/ijms21093042.
8
Robust increases in erythropoietin production by the hypoxic fetus is a response to protect the brain and other vital organs.胎儿在缺氧时会大量产生促红细胞生成素,这是一种保护大脑和其他重要器官的反应。
Pediatr Res. 2018 Dec;84(6):807-812. doi: 10.1038/s41390-018-0054-4. Epub 2018 Jun 12.
9
Effects of erythropoietin receptor activity on angiogenesis, tubular injury, and fibrosis in acute kidney injury: a "U-shaped" relationship.促红细胞生成素受体活性对急性肾损伤中血管生成、肾小管损伤和纤维化的影响:一种“U 型”关系。
Am J Physiol Renal Physiol. 2018 Apr 1;314(4):F501-F516. doi: 10.1152/ajprenal.00306.2017. Epub 2017 Nov 29.
10
Quantification of hypoxia-related gene expression as a potential approach for clinical outcome prediction in breast cancer.缺氧相关基因表达的定量分析作为预测乳腺癌临床结局的一种潜在方法。
PLoS One. 2017 Apr 21;12(4):e0175960. doi: 10.1371/journal.pone.0175960. eCollection 2017.