| Literature DB >> 25837384 |
Nathalie Delgehyr1, Alice Meunier1, Marion Faucourt1, Montserrat Bosch Grau2, Laetitia Strehl3, Carsten Janke4, Nathalie Spassky1.
Abstract
Primary and motile cilia differ in their structure, composition, and function. In the brain, primary cilia are immotile signalling organelles present on neural stem cells and neurons. Multiple motile cilia are found on the surface of ependymal cells in all brain ventricles, where they contribute to the flow of cerebrospinal fluid. During development, monociliated ependymal progenitor cells differentiate into multiciliated ependymal cells, thus providing a simple system for studying the transition between these two stages. In this chapter, we provide protocols for immunofluorescence staining of developing ependymal cells in vivo, on whole mounts of lateral ventricle walls, and in vitro, on cultured ependymal cells. We also provide a list of markers we currently use to stain both types of cilia, including proteins at the ciliary membrane and tubulin posttranslational modifications of the axoneme.Entities:
Keywords: Ependymal cells; Multiciliated cells; Neural cells primary culture; Radial glial cells; Tubulin (poly)glutamylation; Tubulin (poly)glycylation; Tubulin detyrosination; Whole mount lateral ventricular walls
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Year: 2015 PMID: 25837384 DOI: 10.1016/bs.mcb.2015.01.004
Source DB: PubMed Journal: Methods Cell Biol ISSN: 0091-679X Impact factor: 1.441