Transplantation Unit, Renal Division, Department of Medicine, University Health Center of Quebec, Faculty of Medicine, Laval University, Québec, QC, Canada.
Transplantation Unit, Renal Division, Department of Medicine, University Health Center of Quebec, Faculty of Medicine, Laval University, Québec, QC, Canada.
Hum Immunol. 2021 Apr;82(4):309-314. doi: 10.1016/j.humimm.2021.02.009. Epub 2021 Feb 27.
Derivation of endothelial colony forming cells (ECFCs) from peripheral blood mononuclear cells (PBMCs) is a technique that could provide access to donor endothelial cells to study donor endothelium/recipient immune cells interactions. The success rate of ECFC colony formation from cryopreserved PBMCs has not been reported. We used biobanked PBMCs and studied the yield of ECFC generation. Endothelial phenotype was confirmed with CD31, CD146, CD309, CD34, CD14 and CD11c staining by flow cytometry and VE-cadherin, von Willebrand factor and Dil-Ac-LDL by fluorescent microscopy. Functionality was tested by endothelial cell tube-based formation assay. The success rate of ECFC generation was 28%. Freezing time was not a predictor of ECFC generation while a shorter time on dialysis and living transplant were significant determinants. These data suggest that it is possible to generate ECFCs from cryopreserved PBMCs, which is a potentially useful option for the longitudinal assessment of alloimmune response in transplantation.
从外周血单核细胞 (PBMC) 中分离内皮细胞集落形成细胞 (ECFC) 是一种可以获得供体内皮细胞的技术,用于研究供体内皮细胞/受者免疫细胞相互作用。然而,从冷冻保存的 PBMC 中形成 ECFC 集落的成功率尚未报道。本研究使用生物银行 PBMC,并研究了 ECFC 生成的产量。通过流式细胞术用 CD31、CD146、CD309、CD34、CD14 和 CD11c 染色,荧光显微镜用 VE-钙粘蛋白、血管性血友病因子和 Dil-Ac-LDL 对内皮表型进行了确认。通过基于内皮细胞管的形成测定来测试功能。ECFC 生成的成功率为 28%。冷冻时间不是 ECFC 生成的预测因素,而透析时间和活体移植时间较短是显著的决定因素。这些数据表明,从冷冻保存的 PBMC 中生成 ECFC 是可能的,这对于移植中的同种免疫反应的纵向评估是一种潜在有用的选择。