Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT 06509, USA.
Exp Hematol. 2010 Jul;38(7):564-73. doi: 10.1016/j.exphem.2010.04.011. Epub 2010 May 4.
Studies on the ability of bone marrow-derived cells to adopt the morphology and protein expression pattern of epithelial cells in vivo have expanded rapidly during the last decade, and hundreds of publications report that bone marrow-derived cells can become epithelial cells of multiple organs, including lung, liver, gastrointestinal tract, skin, pancreas, and others. In this review, we critically evaluate the literature related to engraftment of bone marrow-derived cells as epithelial cells in the lung. More than 40 articles focused on whether bone marrow cells can differentiate into lung epithelial cells have been published, nearly all of which claim to identify marrow-derived epithelial cells. A few investigations have concluded that no such cells are present and that the phenomenon of marrow-derived epithelial cells is based on detection artifacts. Here we discuss the problems that exist in published articles identifying marrow-derived epithelial cells, and propose standards for detection methods that provide the most definitive data. Identification of bone marrow-derived epithelial cells requires reliable and sensitive techniques for their detection, which must include cell identification based on the presence of an epithelial marker and the absence of blood cell markers as well as a marker for donor bone marrow origin. In order for these studies to be rigorous, they must also use approaches to rule out cell overlap by microscopy or single-cell isolation. Once these stringent criteria for identification of marrow-derived epithelial cells are used universally, then the field can move forward to address the critical questions about which bone marrow-derived cells are responsible for engraftment as epithelial cells, the mechanisms by which this occurs, whether these cells play a role in normal tissue repair, and whether specific cell subsets can be used for therapeutic benefit.
在过去的十年中,关于骨髓细胞在体内获得上皮细胞形态和蛋白表达模式的能力的研究迅速发展,数百篇文献报道骨髓细胞可成为多种器官的上皮细胞,包括肺、肝、胃肠道、皮肤、胰腺等。在这篇综述中,我们批判性地评估了与骨髓细胞作为肺上皮细胞植入相关的文献。已经发表了 40 多篇关于骨髓细胞是否可以分化为肺上皮细胞的文章,几乎所有这些文章都声称可以识别骨髓来源的上皮细胞。少数研究得出的结论是不存在这种细胞,骨髓来源的上皮细胞现象是基于检测假象。在这里,我们讨论了在已发表的文章中识别骨髓来源的上皮细胞存在的问题,并提出了检测方法的标准,这些标准提供了最明确的数据。识别骨髓来源的上皮细胞需要可靠和敏感的检测技术,这些技术必须包括基于上皮标志物存在和血细胞标志物以及供体骨髓来源标志物不存在的细胞识别。为了使这些研究严格,它们还必须采用通过显微镜或单细胞分离排除细胞重叠的方法。一旦普遍使用这些严格的骨髓来源上皮细胞鉴定标准,该领域就可以进一步探讨哪些骨髓来源细胞负责作为上皮细胞植入、发生这种情况的机制、这些细胞是否在正常组织修复中发挥作用以及是否可以使用特定的细胞亚群来获得治疗益处等关键问题。