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作为小鼠气管和人类气道上皮干细胞的基底细胞。

Basal cells as stem cells of the mouse trachea and human airway epithelium.

作者信息

Rock Jason R, Onaitis Mark W, Rawlins Emma L, Lu Yun, Clark Cheryl P, Xue Yan, Randell Scott H, Hogan Brigid L M

机构信息

Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):12771-5. doi: 10.1073/pnas.0906850106. Epub 2009 Jul 22.

Abstract

The pseudostratified epithelium of the mouse trachea and human airways contains a population of basal cells expressing Trp-63 (p63) and cytokeratins 5 (Krt5) and Krt14. Using a KRT5-CreER(T2) transgenic mouse line for lineage tracing, we show that basal cells generate differentiated cells during postnatal growth and in the adult during both steady state and epithelial repair. We have fractionated mouse basal cells by FACS and identified 627 genes preferentially expressed in a basal subpopulation vs. non-BCs. Analysis reveals potential mechanisms regulating basal cells and allows comparison with other epithelial stem cells. To study basal cell behaviors, we describe a simple in vitro clonal sphere-forming assay in which mouse basal cells self-renew and generate luminal cells, including differentiated ciliated cells, in the absence of stroma. The transcriptional profile identified 2 cell-surface markers, ITGA6 and NGFR, which can be used in combination to purify human lung basal cells by FACS. Like those from the mouse trachea, human airway basal cells both self-renew and generate luminal daughters in the sphere-forming assay.

摘要

小鼠气管和人类气道的假复层上皮包含一群表达Trp-63(p63)、细胞角蛋白5(Krt5)和Krt14的基底细胞。利用KRT5-CreER(T2)转基因小鼠系进行谱系追踪,我们发现基底细胞在出生后生长期间以及成年期的稳态和上皮修复过程中都会产生分化细胞。我们通过荧光激活细胞分选(FACS)对小鼠基底细胞进行了分选,并鉴定出627个在基底亚群中相对于非基底细胞优先表达的基因。分析揭示了调节基底细胞的潜在机制,并允许与其他上皮干细胞进行比较。为了研究基底细胞的行为,我们描述了一种简单的体外克隆球形成试验,在该试验中,小鼠基底细胞在没有基质的情况下自我更新并产生管腔细胞,包括分化的纤毛细胞。转录谱鉴定出2种细胞表面标志物,整合素α6(ITGA6)和神经生长因子受体(NGFR),它们可联合用于通过FACS纯化人肺基底细胞。与人气管的基底细胞一样,人气道基底细胞在球形成试验中既能自我更新又能产生管腔子代细胞。

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