Shortt Alex J, Secker Genevieve A, Munro Peter M, Khaw Peng T, Tuft Stephen J, Daniels Julie T
MRC Clinical Research Fellow, Institute of Ophthalmology and Moorfields Eye Hospital, 11-43 Bath Street, London, EC1V 9EL, United Kingdom.
Stem Cells. 2007 Jun;25(6):1402-9. doi: 10.1634/stemcells.2006-0580. Epub 2007 Mar 1.
It is anticipated that stem cell (SC) therapy will enable the regeneration of diseased tissues and organs. Understanding SC niches is an essential step toward realizing this goal. By virtue of its optical transparency and physical separation of SC and transient amplifying cell compartments, the human cornea provides a unique opportunity to visualize and observe a population of adult stem cells, limbal epithelial stem cells (LESCs), in their niche environment. To date, the characteristics of the LESC niche have remained unclear. State-of-the-art imaging techniques were used to construct a three-dimensional (3D) view of the entire human corneal limbus and identify the structural characteristics of the LESC niche. Two distinct candidate LESC niche structures were identified. Cells within these structures express high levels of the putative limbal stem cell markers p63alpha and ABCG2; however, current methods cannot identify for certain which exact cells within this cell population are truly LESCs. These structures could be located and observed in vivo in normal human subjects, but not in patients with clinically diagnosed corneal LESC deficiency. The distribution of these structures around the corneal circumference is not uniform. Biopsies targeted to limbal regions rich in LESC niche structures yielded significantly higher numbers of LESCs in culture. Our findings demonstrate how adult stem cell niches can be identified and observed in vivo in humans and provide new biological insight into the importance of LESC niche structures in maintaining normal LESC function. Finally, the concept of targeted biopsy of adult SC niches improves stem cell yield and may prove to be essential for the successful development of novel adult stem cell therapies. Disclosure of potential conflicts of interest is found at the end of this article.
预计干细胞(SC)疗法将能够实现患病组织和器官的再生。了解干细胞生态位是实现这一目标的关键一步。凭借其光学透明性以及干细胞和短暂增殖细胞区室的物理分离,人类角膜为可视化和观察成年干细胞群体——角膜缘上皮干细胞(LESCs)在其生态位环境中的情况提供了独特机会。迄今为止,角膜缘上皮干细胞生态位的特征仍不明确。利用最先进的成像技术构建了整个人类角膜缘的三维(3D)视图,并确定了角膜缘上皮干细胞生态位的结构特征。识别出了两种不同的候选角膜缘上皮干细胞生态位结构。这些结构内的细胞表达高水平的假定角膜缘干细胞标志物p63α和ABCG2;然而,目前的方法无法确切确定该细胞群体中哪些细胞才是真正的角膜缘上皮干细胞。这些结构能够在正常人类受试者体内定位和观察到,但在临床诊断为角膜缘上皮干细胞缺乏症的患者体内则观察不到。这些结构在角膜圆周周围的分布并不均匀。针对富含角膜缘上皮干细胞生态位结构的角膜缘区域进行活检,在培养中获得的角膜缘上皮干细胞数量显著更多。我们的研究结果展示了如何在人类体内识别和观察成年干细胞生态位,并为角膜缘上皮干细胞生态位结构在维持正常角膜缘上皮干细胞功能中的重要性提供了新的生物学见解。最后,成年干细胞生态位靶向活检的概念提高了干细胞产量,可能对新型成年干细胞疗法的成功开发至关重要。潜在利益冲突的披露见本文末尾。