首页> 外文期刊>Stem cells international >Alteration in Marrow Stromal Microenvironment and Apoptosis Mechanisms Involved in Aplastic Anemia: An Animal Model to Study the Possible Disease Pathology
【24h】

Alteration in Marrow Stromal Microenvironment and Apoptosis Mechanisms Involved in Aplastic Anemia: An Animal Model to Study the Possible Disease Pathology

机译:再生障碍性贫血涉及的骨髓基质微环境的改变和凋亡机制:研究可能疾病病理的动物模型

获取原文
           

摘要

Aplastic anemia (AA) is a heterogeneous disorder of bone marrow failure syndrome. Suggested mechanisms include a primary stem cell deficiency or defect, a secondary stem cell defect due to abnormal regulation between cell death and differentiation, or a deficient microenvironment. In this study, we have tried to investigate the alterations in hematopoietic microenvironment and underlying mechanisms involved in such alterations in an animal model of drug induced AA. We presented the results of studying long term marrow culture, marrow ultra-structure, marrow adherent and hematopoietic progenitor cell colony formation, flowcytometric analysis of marrow stem and stromal progenitor populations and apoptosis mechanism involved in aplastic anemia. The AA marrow showed impairment in cellular proliferation and maturation and failed to generate a functional stromal microenvironment even after 19 days of culture. Ultra-structural analysis showed a degenerated and deformed marrow cellular association in AA. Colony forming units (CFUs) were also severely reduced in AA. Significantly decreased marrow stem and stromal progenitor population with subsequently increased expression levels of both the extracellular and intracellular apoptosis inducer markers in the AA marrow cells essentially pointed towards the defective hematopoiesis; moreover, a deficient and apoptotic microenvironment and the microenvironmental components might have played the important role in the possible pathogenesis of AA.
机译:再生障碍性贫血(AA)是一种骨髓衰竭综合征的异质性疾病。建议的机制包括原发性干细胞缺乏或缺陷,由于细胞死亡与分化之间异常调控而引起的继发性干细胞缺陷或微环境不足。在这项研究中,我们试图研究药物诱导的AA动物模型中造血微环境的改变以及与这种改变有关的潜在机制。我们介绍了研究长期骨髓培养,骨髓超微结构,骨髓粘附和造血祖细胞集落形成,骨髓干和基质祖细胞的流式细胞术分析和再生障碍性贫血所涉及的凋亡机制的研究结果。 AA骨髓显示出细胞增殖和成熟受损,甚至在培养19天后也无法产生功能性基质微环境。超结构分析显示AA中变性和变形的骨髓细胞缔合。菌落形成单位(CFUs)的AA也大大降低。骨髓干细胞和基质祖细胞数量显着减少,而AA骨髓细胞中细胞外和细胞内凋亡诱导剂标志物的表达水平随后升高,这基本上表明造血功能缺陷。此外,缺乏和凋亡的微环境和微环境成分可能在机管局的可能发病机制中发挥了重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号