Experiments on the use of DAMP to study retina and cultured neurons.
Author(s) -
E Augenbraun,
David Sulzer,
Stephen Rayport,
Wanda Setlik,
E Holtzman
Publication year - 1990
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 - 10.1177/38.12.1701464
Subject(s) - damp , horseradish peroxidase , endocytic cycle , retina , microbiology and biotechnology , intracellular , immunocytochemistry , biophysics , chemistry , biology , biochemistry , neuroscience , cell , enzyme , endocrinology , endocytosis , physics , meteorology
Immunocytochemical localization of DAMP, a reagent used to detect low pH intracellular compartments, was studied in cultured neurons from rat hippocampus and in frog retinas. We find that DAMP is more sharply localized and that the immunocytochemical reaction is stronger when horseradish peroxidase or other proteins are included in the medium used to administer DAMP to the cells. A likely explanation is that the proteins enter acidified endocytic compartments and there provide sites to which DAMP molecules can be attached during fixation.
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