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Cell Cycle Synchronization of the Murine EO771 Cell Line Using Double Thymidine Block Treatment

Authors :
Adrien Rossary
Delphine Le Guennec
Marie Goepp
Marie-Paule Vasson
Unité de Nutrition Humaine (UNH)
Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
Centre Jean Perrin [Clermont-Ferrand] (UNICANCER/CJP)
UNICANCER
PhD fellowship (Delphine Le Guennec) from la Ligue nationale contre le cancer
Source :
BioEssays, BioEssays, 2020, 42 (9), pp.1900116. ⟨10.1002/bies.201900116⟩, BioEssays, Wiley-VCH Verlag, 2020, 42 (9), pp.1900116. ⟨10.1002/bies.201900116⟩
Publication Year :
2020
Publisher :
HAL CCSD, 2020.

Abstract

International audience; This study shows that double thymidine block treatment efficiently arrests the EO771 cells in the S-phase without altering cell growth or survival. A long-term analysis of cell behavior, using 5(6)-carboxyfluorescein diacetate N-succinimidyl ester (CFSE) staining, show synchronization to be stable and consistent over time. The EO771 cell line is a medullary breast-adenocarcinoma cell line isolated from a spontaneous murine mammary tumor, and can be used to generate murine tumor implantation models. Different biological (serum or amino acid deprivation), physical (elutriation, mitotic shake-off), or chemical (colchicine, nocodazole, thymidine) treatments are widely used for cell synchronization. Of the different methods tested, the double thymidine block is the most efficient for synchronization of murine EO771 cells if a large quantity of highly synchronized cells is recommended to study functional and biochemical events occurring in specific points of cell cycle progression.

Details

Language :
English
ISSN :
02659247 and 15211878
Database :
OpenAIRE
Journal :
BioEssays, BioEssays, 2020, 42 (9), pp.1900116. ⟨10.1002/bies.201900116⟩, BioEssays, Wiley-VCH Verlag, 2020, 42 (9), pp.1900116. ⟨10.1002/bies.201900116⟩
Accession number :
edsair.doi.dedup.....3d99d5cedc3a9e37f6a0d37025b6c3c7
Full Text :
https://doi.org/10.1002/bies.201900116⟩