| Literature DB >> 29435937 |
Alyne Simões1,2, Zujian Chen3, Yan Zhao1, Lin Chen1, Virgilia Macias4, Luisa A DiPietro1,5, Xiaofeng Zhou6,7,8,9.
Abstract
MicroRNAs are ~22 nucleotide-long noncoding RNAs influencing many cellular processes (including wound healing) by their regulatory functions on gene expression. The ability to analyze microRNA in different cells at the wound site is essential for understanding the critical role(s) of microRNA during various phases of wound healing. Laser capture micro-dissection (LCM) is an effective method to distinguish between relevant and non-relevant cells or tissues and enables the researcher to obtain homogeneous, ultra-pure samples from heterogeneous starting material. We present here our protocol for procuring epithelial cells from a mouse wound healing model using a Leica LMD7000 Laser Microdissection system, as well as the RNA isolation and downstream microRNA analysis. Using this method, researchers can selectively and routinely analyze regions of interest down to single cells to obtain results that are relevant, reproducible, and specific.Entities:
Keywords: Epithelial cells; Frozen sample; LCM; MicroRNA; Mouse; RNA isolation; Wound healing
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Year: 2018 PMID: 29435937 PMCID: PMC5997841 DOI: 10.1007/978-1-4939-7601-0_19
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745