Metabolism, migration and memory in cytotoxic T cells View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2011-02

AUTHORS

David Finlay, Doreen A. Cantrell

ABSTRACT

The transcriptional and metabolic programmes that control CD8(+) T cells are regulated by a diverse network of serine/threonine kinases. The view has been that the kinases AKT and mammalian target of rapamycin (mTOR) control T cell metabolism. Here, we challenge this paradigm and discuss an alternative role for these kinases in CD8(+) T cells, namely to control cell migration. Another emerging concept is that AMP-activated protein kinase (AMPK) family members control T cell metabolism and determine the effector versus memory fate of CD8(+) T cells. We speculate that one link between metabolism and immunological memory is provided by kinases that originally evolved to control T cell metabolism and have subsequently acquired the ability to control the expression of key transcription factors that regulate CD8(+) T cell effector function and migratory capacity. More... »

PAGES

109

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/nri2888

DOI

http://dx.doi.org/10.1038/nri2888

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1037979335

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/21233853


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