Croissant Coralie, Bouvet Flora, Tan Sisareuth, Bouter Anthony
Institute of Chemistry and Biology of Membranes and Nano-objects, UMR 5248, CNRS, University of Bordeaux, Pessac, France.
Curr Protoc Cell Biol. 2018 Dec;81(1):e55. doi: 10.1002/cpcb.55. Epub 2018 Aug 7.
Many cells possess the ability to repair plasma membrane disruption in physiological conditions. Growing evidence indicates a correlation between membrane repair and many human diseases. For example, a negative correlation is observed in muscle where failure to reseal sarcolemma may contribute to the development of muscular dystrophies. Instead, a positive correlation is observed in cancer cells where membrane repair may be exacerbated during metastasis. Here we describe a protocol that combines laser technology for membrane damage, immunostaining with gold nanoparticles and imaging by fluorescence microscopy and transmission electron microscopy (TEM), which allows the characterization of the molecular machinery involved in membrane repair. Fluorescence microscopy enables to determine the subcellular localization of candidate proteins in damaged cells while TEM offers high-resolution ultrastructural analysis of the µm²-disruption site, which enables to decipher the membrane repair mechanism. Here we focus on the study of human skeletal muscle cells, for obvious clinical interest, but this protocol is also suitable for other cell types. © 2018 by John Wiley & Sons, Inc.
许多细胞在生理条件下具备修复质膜破坏的能力。越来越多的证据表明膜修复与许多人类疾病之间存在关联。例如,在肌肉中观察到负相关,肌膜无法重新封闭可能导致肌肉萎缩症的发展。相反,在癌细胞中观察到正相关,在转移过程中膜修复可能会加剧。在这里,我们描述了一种方案,该方案结合了用于膜损伤的激光技术、金纳米颗粒免疫染色以及荧光显微镜和透射电子显微镜(TEM)成像,这使得能够对参与膜修复的分子机制进行表征。荧光显微镜能够确定受损细胞中候选蛋白的亚细胞定位,而TEM则对微米²大小的破坏位点提供高分辨率超微结构分析,从而能够解读膜修复机制。出于明显的临床兴趣,我们在此专注于对人类骨骼肌细胞的研究,但该方案也适用于其他细胞类型。© 2018约翰威立国际出版公司