Počet záznamů: 1
Isolating dividing neural and brain tumour cells for gene expression profiling
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SYSNO ASEP 0459241 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Isolating dividing neural and brain tumour cells for gene expression profiling Tvůrce(i) Endaya, B. (AU)
Cavanagh, B. (AU)
Alowaidi, F. (AU)
Walker, T. (AU)
de Pennington, N. (GB)
Ng, J.-M. (AU)
Lam, P.Y.P. (SG)
Mackay-Sim, A. (AU)
Neužil, Jiří (BTO-N) RID
Meedeniya, A.C.B. (AU)Zdroj.dok. Journal of Neuroscience Methods. - : Elsevier - ISSN 0165-0270
Roč. 257, JAN 15 2016 (2016), s. 121-133Poč.str. 13 s. Jazyk dok. eng - angličtina Země vyd. NL - Nizozemsko Klíč. slova Cell division ; Click chemistry ; FACS Vědní obor RIV EB - Genetika a molekulární biologie Institucionální podpora BTO-N - RVO:86652036 UT WOS 000366224100012 DOI 10.1016/j.jneumeth.2015.09.020 Anotace Background: The characterisation of dividing brain cells is fundamental for studies ranging from developmental and stem cell biology, to brain cancers. Whilst there is extensive anatomical data on these dividing cells, limited gene transcription data is available due to technical constraints. New method: We focally isolated dividing cells whilst conserving RNA, from culture, primary neural tissue and xenografted glioma tumours, using a thymidine analogue that enables gene transcription analysis. Results: 5-ethynyl-2-deoxyuridine labels the replicating DNA of dividing cells. Once labelled, cultured cells and tissues were dissociated, fluorescently tagged with a revised click chemistry technique and the dividing cells isolated using fluorescence-assisted cell sorting. RNA was extracted and analysed using real time PCR. Proliferation and maturation related gene expression in neurogenic tissues was demonstrated in acutely and 3 day old labelled cells, respectively. An elevated expression of marker and pathway genes was demonstrated in the dividing cells of xenografted brain tumours, with the non-dividing cells showing relatively low levels of expression. Comparison with existing method: BrdU "immune-labelling", the most frequently used protocol for detecting cell proliferation, causes complete denaturation of RNA, precluding gene transcription analysis. This EdU labelling technique, maintained cell integrity during dissociation, minimized copper exposure during labelling and used a cell isolation protocol that avoided cell lysis, thus conserving RNA. Conclusions: The technique conserves RNA, enabling the definition of cell proliferation-related changes in gene transcription of neural and pathological brain cells in cells harvested immediately after division, or following a period of maturation. (C) 2015 Elsevier B.V. All rights reserved. Pracoviště Biotechnologický ústav Kontakt Monika Kopřivová, Monika.Koprivova@ibt.cas.cz, Tel.: 325 873 700 Rok sběru 2017
Počet záznamů: 1