Immunocytochemical detection of peroxisomal β-oxidation enzymes in cryostat and paraffin sections of human post mortem liver
- 1 January 1990
- journal article
- research article
- Published by Springer Nature in Journal of Molecular Histology
- Vol. 22 (1) , 57-62
- https://doi.org/10.1007/bf01962880
Abstract
The immunocytochemical visualization of the peroxisomal β-oxidation enzymes was investigated in three human post mortem liver samples. Acyl-CoA oxidase, bifunctional protein and 3-oxoacyl-CoA thiolase remained immunocytochemically detectable 30, 55 and 72 h after death. Peroxisomes in the parenchymal cells were clearly visualized for light microscopy (paraffin and cryostat sections), using protein A-gold in combination with silver enhancement. In two samples catalase activity became very weak, but catalase antigenicity was well preserved. The findings prove the diagnOstic value of post mortem samples, even after extreme conditions of tissue conservation. The technique of immunocytochemical staining for the peroxisomal β-oxidation enzymes on unmounted cryostat sections has not been reported previously. This method allows a quick diagnOsis of biopsies from patients suspected of peroxisomal disorders.This publication has 19 references indexed in Scilit:
- Post-mortem visualization of peroxisomes in rat and in human liverJournal of Molecular Histology, 1990
- Peroxisomal disorders in neurologyJournal of the Neurological Sciences, 1988
- Detection of peroxisomes in human liver and kidney fixed with formalin and embedded in paraffin: The use of catalase and lipid β-oxidation enzymes as immunocytochemical markersJournal of Molecular Histology, 1988
- Light microscopic visualization of peroxisomes and plasmalogens in first trimester chorionic villiPrenatal Diagnosis, 1987
- Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.Proceedings of the National Academy of Sciences, 1987
- Hepatic peroxisomes are deficient in infantile refsum disease: A cytochemical study of 4 casesAmerican Journal of Medical Genetics, 1986
- Peroxisomal disorders: A newly recognised group of genetic diseasesEuropean Journal of Pediatrics, 1986
- A NEW METHOD OF PREPARING GOLD PROBES FOR MULTIPLE-LABELING CYTO-CHEMISTRY1985
- The Presence of a New 3‐Oxoacyl‐CoA Thiolase in Rat Liver PeroxisomesEuropean Journal of Biochemistry, 1980
- STUDIES ON NECROSIS OF MOUSE LIVER IN VITRO - ULTRASTRUCTURAL ALTERATIONS IN MITOCHONDRIA OF HEPATIC PARENCHYMAL CELLS1965