A novel mitochondria-targeting method using special staining for the detection of apoptotic hepatocytes. (2nd April 2020)

• Record Type: Journal Article
• Authors: Gal, Adrian Florin; Ruxanda, Flavia; Rus, Vasile; Andrei, Sanda; Miclăuş, Viorel
• Is Part Of: Journal of histotechnology. Volume 43:Number 2(2020)
• Page Start: 97
• Page End: 101
• Publication Date: 2020-04-02
• Subjects: Apoptosis -- cell death -- Heidenhains's hematoxylin -- liver -- mitochondria -- kolster's fixative -- necrosis; Histology -- Periodicals; Cytology -- Periodicals; 611.018
• DOI: 10.1080/01478885.2020.1721767
• Languages: English
• ISSNs: 0147-8885

Abstract

ABSTRACT: Early detection of apoptotic cells on histological slides is of major importance for both diagnostic and research areas. In the current study, the aim was to propose a convenient method to stain the mitochondria and establish whether hepatocytes undergoing apoptosis can be identified in tissue sections using the proposed method. Liver tissue from five adult chinchillas was fixed with 10% neutral buffered formalin for Goldner's trichrome (GT) and Groat's iron hematoxylin and eosin (HE) stains and with Kolster's fixative for the Heidenhain's iron hematoxylin procedure. The HE and GT-stained sections showed the morphological features consistent with apoptosis i.e., homogenous intensely acidophilic cytoplasm, cell shrinkage with an irregular outline, nuclear shrinkage with cloudy karyoplasm, and karyopyknosis in the late stage. Sections stained with Heidenhain's iron hematoxylin method was used to pinpoint mitochondria and revealed cells which were undergoing the first stages of the apoptosis process i.e., disappearance of mitochondria from the cell, chromatin condensation and margination, paracentral localization of nucleoli, and vacuolated nuclei. In more advanced stages of apoptosis, cells presented significant nuclear and cytoplasmic changes. It was concluded that this is the first report targeting the mitochondria, by performing inexpensive histological staining techniques, in order to assess dead cells in situ .