Shen Edwin M, Salmeron Lisa V, Sanchez Gabriela, McCloskey Kara E
Graduate Program in Biological Engineering and Small-scale Technologies, University of California, Merced.
School of Engineering, University of California, Merced.
Stem Cell Regen Med. 2024;8(1). Epub 2024 May 26.
Flow cytometry, paired with fluorescent antibodies, is a popular method for characterizing cell phenotypes. Our laboratory is interested in deriving and characterizing vascular smooth muscle cells from embryonic and induced pluripotent stem cells, one of the few stem cell differentiation methods that remain underdeveloped. In our studies, we found that most commercially available antibodies advertised for smooth muscle cell identification using flow-activated cell scanning (FACS) were, in fact, not able to distinguish between positive and negative controls. Attempts to resolve the issues included exploring a range of incubation times, blocking reagents, staining kits, and titrating dilutions against both positive and negative control cells. In the end, we found that only the smooth muscle myosin heavy chain (SMMHC) antibody at a narrow titrating dilution range could distinctly bind to its intended epitope. Moreover, without more adequate and specific antibodies for labelling smooth muscle cells, we were not able to continue with our studies on smooth muscle cell fate.
流式细胞术与荧光抗体相结合,是一种用于表征细胞表型的常用方法。我们的实验室对从胚胎干细胞和诱导多能干细胞中衍生和表征血管平滑肌细胞感兴趣,这是少数仍未充分发展的干细胞分化方法之一。在我们的研究中,我们发现,大多数通过流式激活细胞扫描(FACS)进行平滑肌细胞鉴定的市售抗体实际上无法区分阳性和阴性对照。解决这些问题的尝试包括探索一系列孵育时间、封闭试剂、染色试剂盒,以及针对阳性和阴性对照细胞滴定稀释度。最后,我们发现只有在狭窄滴定稀释范围内的平滑肌肌球蛋白重链(SMMHC)抗体能够特异性结合其预期表位。此外,由于没有更合适、更特异的抗体来标记平滑肌细胞,我们无法继续进行平滑肌细胞命运的研究。