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局部脐带血肾素-血管紧张素系统

Local umbilical cord blood renin-angiotensin system.

作者信息

Goker Hakan, Haznedaroglu Ibrahim C, Beyazit Yavuz, Aksu Salih, Tuncer Serdar, Misirlioglu Muge, Bayramoglu Fatma, Kekilli Murat, Büyükasik Yahya, Sayinalp Nilgun, Ozcebe Osman, Dundar Semra, Mollamahmutoglu Leyla

机构信息

Department of Hematology, Hacettepe University Medical School, Sihhiye, Ankara 06100, Turkey.

出版信息

Ann Hematol. 2005 May;84(5):277-81. doi: 10.1007/s00277-004-0989-x. Epub 2005 Jan 11.

Abstract

Local bone marrow (BM) renin-angiotensin system (RAS) is an autocrine-paracrine system affecting normal and neoplastic hematopoiesis. Angiotensin II type 1a (AT1a) receptors are present on the CD34(+) hematopoietic stem cells (HSC). Angiotensin II stimulates the proliferation and differentiation of the HSC populations through the activation of AT1 receptors on HSC. Umbilical cord blood (UCB) is a rich source of HSC. The existence of a complete local UCB RAS has not been previously investigated. In this study, local synthesis of the major RAS components, namely, angiotensin-converting enzyme (ACE), renin, and angiotensinogen, was identified by demonstrating their corresponding mRNAs using quantitative reverse transcriptase polymerase chain reaction (RT-PCR) in human UCB. Local RAS could regulate cellular growth in a variety of tissues including the BM. Major RAS peptides can exert significant effects on primitive pluripotential HSC populations. Further studies should focus on the interactions between possible autocrine, paracrine, endocrine, and intracrine actions of the local UCB RAS and growth, engraftment, differentiation, and plasticity functions of HSC of UCB origin.

摘要

局部骨髓(BM)肾素-血管紧张素系统(RAS)是一个影响正常和肿瘤性造血的自分泌-旁分泌系统。1a型血管紧张素II(AT1a)受体存在于CD34(+)造血干细胞(HSC)上。血管紧张素II通过激活HSC上的AT1受体来刺激HSC群体的增殖和分化。脐带血(UCB)是HSC的丰富来源。此前尚未研究过完整的局部UCB RAS的存在情况。在本研究中,通过使用定量逆转录聚合酶链反应(RT-PCR)在人UCB中检测主要RAS成分(即血管紧张素转换酶(ACE)、肾素和血管紧张素原)的相应mRNA,确定了它们的局部合成。局部RAS可调节包括BM在内的多种组织中的细胞生长。主要RAS肽可对原始多能HSC群体产生显著影响。进一步的研究应聚焦于局部UCB RAS可能的自分泌、旁分泌、内分泌和胞内分泌作用与UCB来源的HSC的生长、植入、分化和可塑性功能之间的相互作用。

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