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肥大细胞从胚胎干细胞的分化。

Differentiation of mast cells from embryonic stem cells.

作者信息

Kovarova Martina, Koller Beverly

机构信息

Department of Medicine, Division of Pulmonary and Critical Care Medicine, University of North Carolina at Chapel Hill, North Carolina, USA.

出版信息

Curr Protoc Immunol. 2012 Apr;Chapter 22:Unit 22F.10.1-16. doi: 10.1002/0471142735.im22f10s97.

Abstract

In this unit, we describe a simple coculture-free method for obtaining mast cells from mouse and human embryonic stem (ES) cells. Much of our knowledge regarding the mechanisms by which mast cells are activated comes from studies of mouse bone marrow-derived mast cells. Studies of human mast cells have been hampered by the limited sources from which they can be cultured, the difficulty in introducing specific genetic changes into these cells, and differences between established cultures that reflect the unique genetic makeup of the tissue donor. Derivation of mast cells from embryonic stem cells addresses these limitations. ES-derived mast cells can be generated in numbers sufficient for studies of the pathways involved in mast cell effector functions. These ES cell-derived mast cells respond to antigens and other stimuli by releasing histamine, cytokines, lipids, and other bioactive mediators. The derivation of human mast cells from ES cells carrying mutations introduced by homologous recombination should provide a novel means of testing the function of genes in both the development and the effector functions of mast cells.

摘要

在本单元中,我们描述了一种从小鼠和人类胚胎干细胞中获取肥大细胞的简单无共培养方法。我们关于肥大细胞激活机制的许多知识都来自对小鼠骨髓来源肥大细胞的研究。人类肥大细胞的研究受到以下因素的阻碍:可用于培养的来源有限、难以对这些细胞引入特异性基因改变以及已建立的培养物之间的差异反映了组织供体独特的基因组成。从胚胎干细胞中获得肥大细胞解决了这些限制。源自胚胎干细胞的肥大细胞数量足以用于研究肥大细胞效应功能所涉及的途径。这些源自胚胎干细胞的肥大细胞通过释放组胺、细胞因子、脂质和其他生物活性介质来对抗抗原和其他刺激。从携带通过同源重组引入的突变的胚胎干细胞中获得人类肥大细胞,应该为测试基因在肥大细胞发育和效应功能中的作用提供一种新方法。

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