In situ fluorescent visualization of nucleolar organizer region-associated proteins with a thiol reagent.
Author(s) -
G Méhes,
E. Kálmán,
László Pajor
Publication year - 1993
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1177/41.9.8354881
Subject(s) - nucleolus , nucleolus organizer region , silver stain , microbiology and biotechnology , flow cytometry , staining , fluorescence , stain , thiol , biology , chemistry , rnase p , maleimide , fluorescent staining , biochemistry , rna , genetics , gene , nucleus , physics , quantum mechanics , polymer chemistry
Nucleolar organizer regions (NORs) are nucleolus-forming rDNA loops associated with argyrophil proteins, the amount of which varies according to the proliferative state of the cell. It has been presumed that the nucleolar protein-related thiol groups may have a role in selective silver staining. We investigated the nuclear thiol distribution with a fluorescent thiol reagent, coumarinyl-phenyl-maleimide (CPM) in human K-562 myeloblast cultures and found that SH group-related fluorescence was brightest in the area of nucleoli, which became highly selective after RNAse digestion. A remarkable co-localization of AgNOR silver reaction and CPM fluorescence was observed, although occupation of the SH groups by CPM did not prevent the silver staining. We applied the stain to dual-parameter flow cytometry in combination with DNA content measurements, which provide further information on nucleolar function and changes in experimental and pathological specimens.
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