Sensitive fluorescent hybridisation protocol development for simultaneous detection of microRNA and cellular marker proteins (in the retina)

• Published in: Histochemistry and cell biology Vol. 150; no. 5; pp. 557 - 566
• Main Authors: Kovács-Valasek, Andrea, Szalontai, Bálint, Sétáló, György, Gábriel, Robert
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.11.2018; Springer Nature B.V
• Subjects: Animals; Biochemistry; Biomarkers - analysis; Biomedical and Life Sciences; Biomedicine; Cell Biology; Developmental Biology; DNA probes; Endopeptidase K; Gene expression; Gene regulation; Immunofluorescence; Immunohistochemistry; In Situ Hybridization, Fluorescence; Labeling; MicroRNAs; MicroRNAs - analysis; MicroRNAs - metabolism; miRNA; Neurons - chemistry; Neurons - cytology; Neurons - metabolism; Original Paper; Proteinase; Proteins - analysis; Proteins - metabolism; Rats; Rats, Wistar; Retina; Retina - chemistry; Retina - cytology; Retina - metabolism; RNA-mediated interference; Spatial distribution; MicroRNA; mir-9; Tyramide signal amplification; mir-23; In situ hybridisation; Immunocytochemistry
• ISSN: 0948-6143; 1432-119X
• DOI: 10.1007/s00418-018-1705-6

Nowadays, increasing number of microRNAs are found to have crucial roles in various physiological processes through gene expression regulation via RNA silencing as a result of base pairing with complementary mRNA sequences. To reveal the spatial distribution of microRNA expression in tissues, in situ hybridisation is the only method developed to date. This work aims to provide a novel approach to obtain information on the possible involvement of microRNA-s in regulatory processes under experimental conditions by enhancing fluorescent detection of microRNA labelling. Developing Wistar rats were used as a model system to analyse retinal microRNA expression in the first 3 postnatal weeks. Using cryosections, the crucial elements of optimal labels were (1) the concentration and duration of proteinase K treatment, (2) hybridisation temperature of microRNA probes and (3) temperature of stringency washes. Further improvements made possible to combine our in situ hybridisation protocol with double-label immunofluorescence allowing for the simultaneous detection of microRNA-s with high sensitivity and a neuronal cell marker and/or a synaptic marker protein. Thus, the regulatory microRNA-s can be localised in an identified cell type along with its potential target protein. We believe that our protocol can be easily adapted for a variety of tissues of different origins, developmental stages and experimental conditions.