Isolating dividing neural and brain tumour cells for gene expression profiling
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
26432933
DOI
10.1016/j.jneumeth.2015.09.020
PII: S0165-0270(15)00353-2
Knihovny.cz E-resources
- Keywords
- Cell division, Click chemistry, FACS, Gene transcription, Glioma, Stem cells,
- MeSH
- Single-Cell Analysis methods MeSH
- Olfactory Mucosa physiology MeSH
- Click Chemistry MeSH
- Deoxyuridine analogs & derivatives MeSH
- Embryonic Stem Cells physiology MeSH
- Glioma physiopathology MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Brain * physiology physiopathology MeSH
- Mice, Inbred C57BL MeSH
- Mice, Inbred NOD MeSH
- Mice, SCID MeSH
- Brain Neoplasms * physiopathology MeSH
- Neural Stem Cells physiology MeSH
- Neurogenesis * physiology MeSH
- Neurons * physiology MeSH
- RNA metabolism MeSH
- Gene Expression Profiling methods MeSH
- Neoplasm Transplantation MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 5-ethynyl-2'-deoxyuridine MeSH Browser
- Deoxyuridine MeSH
- RNA MeSH
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.
Eskitis Institute for Drug Discovery Griffith University Nathan QLD 4111 Australia
National Cancer Centre Singapore 11 Hospital Drive Singapore 169610 Singapore
References provided by Crossref.org
DNA Replication: From Radioisotopes to Click Chemistry