Flow Cytometric Analysis of the Expression Pattern of Peroxisomal Proteins, Abcd1, Abcd2, and Abcd3 in BV-2 Murine Microglial Cells

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TitreFlow Cytometric Analysis of the Expression Pattern of Peroxisomal Proteins, Abcd1, Abcd2, and Abcd3 in BV-2 Murine Microglial Cells
Type de publicationBook Chapter
Year of Publication2017
AuteursDebbabi M, Nury T, Helali I, Karym EMostafa, Geillon F, Gondcaille C, Trompier D, Najid A, Terreau S, Bezine M, Zarrouk A, Vejux A, Andreoletti P, Cherkaoui-Malki M, Savary S, Lizard G
EditorSchrader M
Book TitlePEROXISOMES: METHODS AND PROTOCOLS
Series TitleMethods in Molecular Biology
Volume1595
Pagination257-265
PublisherHUMANA PRESS INC
City999 RIVERVIEW DR, STE 208, TOTOWA, NJ 07512-1165 USA
ISBN Number978-1-4939-6937-1; 978-1-4939-6935-7
ISBN1064-3745
Mots-clésBV-2 microglial cells, Flow cytometric analysis, Peroxisomal ABC transporters
Résumé

Microglial cells play important roles in neurodegenerative diseases including peroxisomal leukodystrophies. The BV-2 murine immortalized cells are widely used in the context of neurodegenerative researches. It is therefore important to establish the expression pattern of peroxisomal proteins by flow cytometry in these cells. So, the expression pattern of various peroxisomal transporters (Abcd1, Abcd2, Abcd3) contributing to peroxisomal beta-oxidation was evaluated on BV-2 cells by flow cytometry and complementary methods (fluorescence microscopy, and RT-qPCR). By flow cytometry a strong expression of peroxisomal proteins (Abcd1, Abcd2, Abcd3) was observed. These data were in agreement with those obtained by fluorescence microscopy (presence of numerous fluorescent dots in the cytoplasm characteristic of a peroxisomal staining pattern) and RT-qPCR (high levels of Abcd1, Abcd2, and Abcd3 mRNAs). Thus, the peroxisomal proteins (Abcd1, Abcd2, Abcd3) are expressed in BV-2 cells, and can be analyzed by flow cytometry.

DOI10.1007/978-1-4939-6937-1_25