Cytochemistry of membrane proteases
- 1 July 1985
- journal article
- review article
- Published by Springer Nature in Journal of Molecular Histology
- Vol. 17 (7) , 737-771
- https://doi.org/10.1007/bf01003312
Abstract
Summary Membrane proteases that are detectable by cytochemical means are the classified exopeptidases, aminopeptidases A and M (or N), γ-glutamyl transpeptidase (which also acts as transferase), dipeptidyl peptidase IV and the endopeptidase, enteropeptidase (also known as enterokinase). Not yet classified are the possible expeptidase, tripeptidyl peptidase and endopeptidases I (Ala-endopeptidase) and II (Arg-endopeptidase). All these membrane proteases can be investigated with either chromogenic or fluorogenic procedures using synthetic peptide substrates. The most useful substrates are 4-methoxy-2-naphthylamine amino acids and peptides for cytochemical localizations at the light and electron microscope levels, for cytophotometric quantification and the study of membrane protease isoenzymes after analytical isoelectric focusing. Amino acid or peptide derivatives of naphthylamine AS can be recommended for light microscopical localization and cytofluorometric quantification, and 7-amino-4-methylcoumarin and 7-amino-4-trifluoromethylcoumarin amino acids and peptides for the development of enzyme bands after isoelectric focusing. Cytochemistry reveals the heterogeneity in the distribution and species differences of membrane proteases in adult cells, tissues and organs and during development. It also reveals some common localizations, such as in small intestinal enterocytes and proximal tubule cells. The species and organ differences are substantiated and extended considerably by isoelectric focusing in combination with methods for the cytochemical detection of proteases. In addition, continuous cytophotometry or cytofluorometry (section and cultured cell biochemistry) allows the kinetic characteristics, initial reaction rates and maximum activities of all membrane proteases to be determined. The physiological functions of the endopeptidases and exopeptidases are still a matter of debate. However, from cytochemical inhibition studies with natural peptide substrates, e.g. peptide hormones, there is increasing evidence that the proteases detected with synthetic peptides play a decisive role in many physiological circumstances, e.g. in endocrine regulation mechanisms or the regulation of blood pressure. In this respect, capillary endothelium-linked surface membrane proteases may be especially important.Keywords
This publication has 93 references indexed in Scilit:
- Identification of protease isozymes after analytical isoelectric focusing using fluorogenic substrates impregnated into cellulose membranes.Journal of Histochemistry & Cytochemistry, 1984
- Early post-natal development of the brush border enzymes of enterocytes in the rat and mini-pigJournal of Molecular Histology, 1984
- Ultrastructure and enzyme histochemistry of the marmoset yolk sac and embryonic intestinal epitheliumJournal of Molecular Histology, 1984
- Subcellular localization of dipeptidyl peptidases II and IV in rat and rabbit alveolar macrophages.Journal of Histochemistry & Cytochemistry, 1983
- Enzymehistochemical staining of Tμ lymphocytes for glycyl-proline-4-methoxy-beta-naphthylamide-peptidase (DAP IV)British Journal of Haematology, 1982
- Immunohistochemical localization of dipeptidyl aminopeptidase IV in rat kidney, liver, and salivary glands.Journal of Histochemistry & Cytochemistry, 1981
- Proteinases in pathology. Usefulness of histochemical methodsJournal of Histochemistry & Cytochemistry, 1981
- Liver dipeptidyl aminopeptidase IV hydrolyzes substance PFEBS Letters, 1978
- Changes in membrane-bound aminopeptidase on bone marrow-derived macrophages during their maturation in vitroExperimental Cell Research, 1977
- Plasma angiotensinasesBiochemical Medicine, 1967