3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, Portugal.
ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Stem Cell Rev Rep. 2021 Aug;17(4):1406-1419. doi: 10.1007/s12015-021-10128-8. Epub 2021 Feb 4.
When in certain culture conditions, organotypic cultures are able to mimic developmental stages of an organ, generating higher-order structures containing functional subunits and progenitor niches. Despite the major advances in the area, researchers have not been able to fully recapitulate the complexity of kidney tissue. Pluripotent stem cells are extensively used in the field, but very few studies make use of adult stem cells. Herein, we describe a simple and feasible method for achieving glomerular epithelial differentiation on an organotypic model comprising human renal progenitor cells from adult kidney (hRPCs). Their glomerular differentiative potential was studied using retinoic acid (RA), a fundamental molecule for intermediate mesoderm induction on early embryogenesis. Immunofluorescence, specific cell surface markers expression and gene expression analysis confirm the glomerular differentiative potential of RA in a short-term culture. We also compared the potential of RA with a potent WNT agonist, CHIR99021, on the differentiative capacity of hRPCs. Gene expression and immunofluorescence analysis confirmed that hRPCs are more sensitive to RA stimulation when compared to CHIR9901. Endothelial cells were also included on the spheroids, resulting in a higher organizational level. The assembly potential of these cells and their selective stimulation will give new insights on adult organotypic cell culture studies and will hopefully guide more works in this important area of research.
在某些特定的培养条件下,器官型培养能够模拟器官的发育阶段,产生包含功能亚单位和祖细胞龛的高级结构。尽管在该领域取得了重大进展,但研究人员仍未能完全再现肾脏组织的复杂性。多能干细胞在该领域得到了广泛应用,但很少有研究利用成体干细胞。本文描述了一种在包含成人肾脏来源的肾祖细胞(hRPCs)的器官型模型上实现肾小球上皮细胞分化的简单可行的方法。使用视黄酸(RA)研究它们的肾小球分化潜能,视黄酸是早期胚胎发生中中胚层诱导的基本分子。免疫荧光、特定细胞表面标志物表达和基因表达分析证实了 RA 在短期培养中具有肾小球分化潜能。我们还比较了 RA 与强效 WNT 激动剂 CHIR99021 对 hRPCs 分化能力的影响。基因表达和免疫荧光分析证实,与 CHIR9901 相比,hRPCs 对 RA 刺激更为敏感。内皮细胞也被包括在球体中,从而提高了组织水平。这些细胞的组装潜力及其选择性刺激将为成体器官型细胞培养研究提供新的见解,并有望指导该重要研究领域的更多工作。