Department of Medicine, Division of Pulmonary and Critical Care Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Blood. 2010 May 6;115(18):3695-703. doi: 10.1182/blood-2009-08-237206. Epub 2010 Mar 3.
Human mast cells are tissue resident cells with a principal role in allergic disorders. Cross-linking of the high-affinity receptor for immunoglobulin E (FcepsilonRI) results in release of inflammatory mediators initiating the clinical symptoms of allergy and anaphylaxis. Much of our knowledge regarding the mechanisms of mast cell activation comes from studies of mouse bone marrow-derived mast cells. However, clear differences have been identified between human and mouse mast cells. Studies of human mast cells are hampered by the limited sources available for their isolation, the resistance of these cells to genetic manipulation, and differences between cultures established from different persons. To address this limitation, we developed a simple coculture-free method for obtaining mast cells from human embryonic stem cells (hES). These hES-derived mast cells respond to antigen by releasing mast cell mediators. Moreover, the cells can be generated in numbers sufficient for studies of the pathways involved in their effector functions. Genetically modified mast cells, such as GFP-expressing cells, can be obtained by introduction and selection for modification in hES cells before differentiation. This direct coculture-free differentiation of hES cells represents a new and unique model to analyze the function and development of human mast cells.
人类肥大细胞是组织驻留细胞,在过敏疾病中起主要作用。免疫球蛋白 E(IgE)的高亲和力受体(FcεRI)交联导致炎症介质的释放,从而引发过敏和过敏反应的临床症状。我们对肥大细胞激活机制的了解主要来自对鼠骨髓来源的肥大细胞的研究。然而,已经确定人类肥大细胞和鼠肥大细胞之间存在明显差异。由于用于分离的人类肥大细胞的来源有限、这些细胞对遗传操作的抵抗力以及从不同人建立的培养物之间的差异,因此对人类肥大细胞的研究受到阻碍。为了解决这个限制,我们开发了一种从人类胚胎干细胞(hES)中获得肥大细胞的简单无共培养方法。这些 hES 衍生的肥大细胞通过释放肥大细胞介质对抗原作出反应。此外,这些细胞可以大量产生,足以用于研究其效应功能涉及的途径。通过在 hES 细胞分化之前进行引入和修饰选择,可以获得遗传修饰的肥大细胞,如 GFP 表达细胞。这种 hES 细胞的直接无共培养分化代表了分析人类肥大细胞功能和发育的一种新的独特模型。