Rhodamine as a fluorescent probe of lymphocyte activation.
Immunology, 1979/2;36(2):235-40.
Nairn RC, Jablonka IM, Rolland JM, Halliday GM, Ward HA
PMID: 155648
Impact factor: 7.215
Abstract
Fresh rat and mouse lymphoid cells have been labelled by stable linkage with tetramethylrhodamine isothiocyanate (TMRITC). A change in intensity, either an increase or decrease of the fluorescent emission of the cells, detected by microfluorimetry, was induced by mitogen stimulation or the mixed lymphocyte reaction. The change in fluorescence was observed within 3 h of mitogen stimulation and within 0.5 h in the mixed lymphocyte test. These early cellular responses were detectable consistently whether the labelling was done before or after mitogen stimulation; post-labelling only was studied in the mixed lymphocyte reaction. The method should provide a time-saving practical procedure for early detection of the lymphoid cell responses and would readily lend itself to flow cytofluorimetry for possible routine diagnostic use.
MeSH terms
Animals; Concanavalin A; Lymphocyte Activation; Lymphocyte Culture Test, Mixed; Lymphocytes; Mice; Mice, Inbred Strains; Microscopy, Fluorescence; Phytohemagglutinins; Pokeweed Mitogens; Rats; Rhodamines; Spectrometry, Fluorescence; Xanthenes
More resources
Full text:
Europe PubMed Central; PubMed Central
EndNote: Download