Immunocytochemical studies of pituitary hormones with PAP, ABC, and immunogold techniques: Evolution of technology to best fit the antigen
- 1 February 1986
- journal article
- research article
- Published by Wiley in Journal of Anatomy
- Vol. 175 (2-3) , 307-330
- https://doi.org/10.1002/aja.1001750214
Abstract
The immunocytochemical technology in our laboratory has evolved in response to specific needs for more efficient, refined stains for each antigen. The rationale for the application of each of the immunocytochemical techniques used today is described, and detailed methods are given. In the early 1970s, it was determined that the peroxidase-antiperoxidase complex (PAP) stain provided the most sensitive means of detection of adrenocorticotropin (ACTH) at the electron microscope level even in tissues prepared with conventional fixation and embedding techniques that are considered rather harsh for the maintenance of antigenicity. Application of the same PAP complex technique to the larger glycoprotein antigens, like follicle-stimulating hormone (FSH), however, proved far more difficult; and the problem was resolved partially when more gentle fixation-embedding protocols were applied. The production of an efficient, reliable stain for FSH was achieved only with the avidin-biotin peroxidase complex (ABC) stains were applied in the early 1980s. This technique also allowed more efficient reactions for all the antigens, and morphometric data could thereby be collected more rapidly. Thus, we concluded that the light microscope immunoperoxidase techniques were excellent for the morphometric analysis of pituitary cell types in both pre-embedding and postembedding stains. However, the need for a more refined stain for its quantification at the electron microscope level on individual organelles led to the development of the colloidal gold stain in 1983–1984. This technique, which is new to our laboratory, is also described and illustrated in this report. Also included is a description of our studies of the effect of fixation and embedding processes on hormone antigenicity and techniques used to control background and nonspecific reactions. It is hoped that the novice will find the description of the rationale for the evolution of technology in our laboratory useful in making choices for his or her own immunocytochemical stains.This publication has 29 references indexed in Scilit:
- Shifts in gonadotropin storage in cultured gonadotropes following GnRH stimulation, in vitroPeptides, 1985
- Visualization of peptide-immunoreactive processes on serotonin-immunoreactive cells using two-color immunoperoxidase staining.Journal of Histochemistry & Cytochemistry, 1984
- Ultrastructural localization of antigenic sites on osmium-fixed tissues applying the protein A-gold technique.Journal of Histochemistry & Cytochemistry, 1983
- The Use of Multiple Methods to Validate Immunocytochemical StainsJournal of Histochemistry & Cytochemistry, 1983
- Application of a rapid avidin--biotin--peroxidase complex (ABC) technique to the localization of pituitary hormones at the electron microscopic level.Journal of Histochemistry & Cytochemistry, 1982
- Application of the avidin-biotin-peroxidase complex (ABC) method to the light microscopic localization of pituitary hormones.Journal of Histochemistry & Cytochemistry, 1982
- Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures.Journal of Histochemistry & Cytochemistry, 1981
- DAB cytochemistry: artifact problems in its current uses.Journal of Histochemistry & Cytochemistry, 1980
- DIFFUSION ARTIFACTS IN 3,3'-DIAMINOBENZIDINE CYTOCHEMISTRYJournal of Histochemistry & Cytochemistry, 1972
- ELECTRON MICROSCOPIC STUDY OF THE ADRENOCORTICOTROPIN-PRODUCING CELL WITH THE USE OF UNLABELED ANTIBODY AND THE SOLUBLE PEROXIDASE-ANTIPEROXIDASE COMPLEXJournal of Histochemistry & Cytochemistry, 1972