The role of inflammatory cytokines as key modulators of neurogenesis
Trends in Neurosciences, ISSN: 0166-2236, Vol: 38, Issue: 3, Page: 145-157
2015
- 297Citations
- 490Captures
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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
- Citations297
- Citation Indexes297
- 297
- CrossRef277
- Captures490
- Readers490
- 490
Review Description
Neurogenesis is an important process in the regulation of brain function and behaviour, highly active in early development and continuing throughout life. Recent studies have shown that neurogenesis is modulated by inflammatory cytokines in response to an activated immune system. To disentangle the effects of the different cytokines on neurogenesis, here we summarise and discuss in vitro studies on individual cytokines. We show that inflammatory cytokines have both a positive and negative role on proliferation and neuronal differentiation. Hence, this strengthens the notion that inflammation is involved in molecular and cellular mechanisms associated with complex cognitive processes and, therefore, that alterations in brain–immune communication are relevant to the development of neuropsychiatric disorders.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0166223614002343; http://dx.doi.org/10.1016/j.tins.2014.12.006; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84924541568&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/25579391; https://linkinghub.elsevier.com/retrieve/pii/S0166223614002343; https://dx.doi.org/10.1016/j.tins.2014.12.006
Elsevier BV
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