| Literature DB >> 34463186 |
Takuya Ikenari1, Tatsuya Kawaguchi2, Rei Ota1, Miki Matsui1, Ryota Yoshida1, Tetsuji Mori1.
Abstract
Fluoro-Jade C (FJC) staining has been used to detect degenerating neurons in tissue sections. It is a simple and easy staining procedure and does not depend on the manner of cell death. In some experiments, double staining with FJC and fluorescent immunostaining (FI) is required to identify cell types. However, pretreatment for FJC staining contains some processes that are harsh to fluorophores, and the FI signal is greatly reduced. To overcome this issue, we improved the double staining protocol to acquire clear double-stained images by introducing the labeled streptavidin-biotin system. In addition, several studies indicate that FJC can label non-degenerating glial cells, including resting/reactive astrocytes and activated microglia. Moreover, our previous study indicated that degenerating mesenchymal cells were also labeled by FJC, but it is still unclear whether FJC can label degenerating glial cells. Acute encephalopathy model mice contained damaged astrocytes with clasmatodendrosis, and 6-aminonicotinamide-injected mice contained necrotic astrocytes and oligodendrocytes. Using our improved double staining protocol with FJC and FI, we detected FJC-labeled degenerating astrocytes and oligodendrocytes with pyknotic nuclei. These results indicate that FJC is not specific to degenerating neurons in some experimental conditions.Entities:
Keywords: damaged cells; glia; histochemistry; improved protocol; injury
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Year: 2021 PMID: 34463186 PMCID: PMC8427928 DOI: 10.1369/00221554211043340
Source DB: PubMed Journal: J Histochem Cytochem ISSN: 0022-1554 Impact factor: 4.137