An overview of in vitro methods to study microglia
Frontiers in Cellular Neuroscience, ISSN: 1662-5102, Vol: 12, Page: 242
2018
- 155Citations
- 720Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations155
- Citation Indexes155
- 155
- Captures720
- Readers720
- 720
Review Description
Neuroinflammation is a common feature in neurodegenerative diseases and strategies to modulate neuroinflammatory processes are increasingly considered as therapeutic options. In such strategies, glia cells rather than neurons represent the cellular targets. Microglia, the resident macrophages of the central nervous system, are principal players in neuroinflammation and detailed cellular biological knowledge of this particular cell type is therefore of pivotal importance. The last decade has shed new light on the origin, characteristics and functions of microglia, underlining the need for specific in vitro methodology to study these cells in detail. In this review we provide a comprehensive overview of existing methodology such as cell lines, stem cell-derived microglia and primary dissociated cell cultures, as well as discuss recent developments. As there is no in vitro method available yet that recapitulates all hallmarks of adult homeostatic microglia, we also discuss the advantages and limitations of existing models across different species.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85053370764&origin=inward; http://dx.doi.org/10.3389/fncel.2018.00242; http://www.ncbi.nlm.nih.gov/pubmed/30127723; https://www.frontiersin.org/article/10.3389/fncel.2018.00242/full; https://dx.doi.org/10.3389/fncel.2018.00242; https://www.frontiersin.org/journals/cellular-neuroscience/articles/10.3389/fncel.2018.00242/full
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