z-logo
open-access-imgOpen Access
Localization of organ-specific antigens in mouse lung by light and electron microscopy.
Author(s) -
W. Nathrath,
C Rowlatt,
F Detheridge
Publication year - 1981
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 - 10.1177/29.12.7033364
Subject(s) - immunoperoxidase , electron microscope , pathology , lamellar granule , chemistry , antiserum , lung , staining , birbeck granules , micrometer , immunofluorescence , antigen , biology , antibody , langerhans cell , ultrastructure , immunology , medicine , physics , monoclonal antibody , optics
Rabbit antisera were raised against whole homogenate and a saline soluble fraction of C57BL mouse lung. After absorption with other mouse organs, both antisera gave specific staining of bronchiolar epithelial and single alveolar cells, using the indirect immunofluorescence and indirect immunoperoxidase techniques on both acetic-alcohol-fixed paraffin-embedded and unfixed frozen 5 micrometer sections. Improved resolution by light microscopy was achieved with 1 micrometer sections of formaldehyde-fixed Araldite-embedded material stained by an indirect immunoperoxidase method after the Araldite had been treated with saturated alcoholic NaOH for 5 min. Clara cells and type II pneumocytes were identifiable as sites of the lung-specific immune reaction. At the electron microscopic level the reaction was localized over the granules of bronchiolar Clara cells. The lamellar bodies of type II pneumocytes were extracted in the ultrathin sections and no immune reaction was observed.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom