Lei Zhiyong, van Mil Alain, Xiao Junjie, Metz Corina H G, van Eeuwijk Esther C M, Doevendans Pieter A, Sluijter Joost P G
Department of Cardiology, Division Heart and Lungs, University Medical Center Utrecht, Utrecht, The Netherlands.
UMC Utrecht Regenerative Medicine Center, University Medical Center, Utrecht 3584CT, The Netherlands.
Biotechnol Rep (Amst). 2018 May 1;18:e00255. doi: 10.1016/j.btre.2018.e00255. eCollection 2018 Jun.
To understand and assess the roles of miRNAs, visualization of the expression patterns of specific miRNAs is needed at the cellular level in a wide variety of different tissue types. Although miRNA hybridization techniques have been greatly improved in recent years, they remain difficult to routinely perform due to the complexity of the procedure. In addition, as it is crucial to define which tissues or cells are expressing a particular miRNA in order to elucidate the biological function of the miRNA, incorporation of additional stainings for different cellular markers is necessary. Here, we describe a robust and flexible multicolor miRNA hybridization (MMISH) technique for paraffin embedded sections. We show that the miRNA protocol is sensitive and highly specific and can successfully be combined with both immunohistochemical and immunofluorescent stainings.
为了理解和评估微小RNA(miRNA)的作用,需要在细胞水平上对多种不同组织类型中特定miRNA的表达模式进行可视化。尽管近年来miRNA杂交技术有了很大改进,但由于操作过程复杂,仍难以常规开展。此外,为了阐明miRNA的生物学功能,确定哪些组织或细胞表达特定的miRNA至关重要,因此需要加入针对不同细胞标志物的额外染色。在此,我们描述了一种用于石蜡包埋切片的稳健且灵活的多色miRNA杂交(MMISH)技术。我们表明,该miRNA方案灵敏且高度特异,并且可以成功地与免疫组织化学和免疫荧光染色相结合。