C. Boutin, Y. Roche, R. Jaffiol, J. Millot, C. Millot, J. Plain, R. Déturche, P. Jeannesson, M. Manfait, P. Royer
{"title":"Effect of different agents onto multidrug resistant cells revealed by fluorescence correlation spectroscopy","authors":"C. Boutin, Y. Roche, R. Jaffiol, J. Millot, C. Millot, J. Plain, R. Déturche, P. Jeannesson, M. Manfait, P. Royer","doi":"10.1051/ANPHYS:2008027","DOIUrl":null,"url":null,"abstract":"Fluorescence correlation spectroscopy (FCS) has been used to analyze the plasma membrane fluidity and heterogene- ity of multidrug resistant cells. At the single cell level, the effects of different membrane agents present in the extra-cellular medium have been explored. Firstly, we reveal a modification of plasma membrane heterogeneities according to the addition of a fluidity modulator, benzyl alcohol. On the other hand, revertants such as verapamil and cyclosporin-A appear to act more specifically on the slow diffusion sites, such as lipids microdomains.","PeriodicalId":50779,"journal":{"name":"Annales De Physique","volume":"10 1","pages":"139-141"},"PeriodicalIF":0.0000,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annales De Physique","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1051/ANPHYS:2008027","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Fluorescence correlation spectroscopy (FCS) has been used to analyze the plasma membrane fluidity and heterogene- ity of multidrug resistant cells. At the single cell level, the effects of different membrane agents present in the extra-cellular medium have been explored. Firstly, we reveal a modification of plasma membrane heterogeneities according to the addition of a fluidity modulator, benzyl alcohol. On the other hand, revertants such as verapamil and cyclosporin-A appear to act more specifically on the slow diffusion sites, such as lipids microdomains.