Advanced search
Start date
Betweenand
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Deciphering targets of Th17 cells fate: From metabolism to nuclear receptors

Full text
Author(s):
Boldrini, Vinicius de Oliveira [1, 2, 3] ; Farias, Alessandro dos Santos [1, 2, 3] ; Degasperi, Giovanna Rosa [4]
Total Authors: 3
Affiliation:
[1] Univ Estadual Campinas, Inst Biol, Dept Genet Microbiol & Immunol, Autoimmune Res Lab, Campinas, SP - Brazil
[2] Univ Estadual Campinas, Inst Biol, Dept Genet Evolut Microbiol & Immunol, Neuroimmunol Unit, Campinas, SP - Brazil
[3] Natl Inst Sci & Technol Neuroimmunomodulat INCT N, Rio De Janeiro - Brazil
[4] Pontificia Univ Catolica Campinas PUC Campinas, Campinas, SP - Brazil
Total Affiliations: 4
Document type: Review article
Source: Scandinavian Journal of Immunology; v. 90, n. 4 JULY 2019.
Web of Science Citations: 0
Abstract

Evidence indicates that reprogramming of metabolism is critically important for the differentiation of CD4 + T lymphocytes, and the manipulation of metabolic pathways in these cells may shape their fate and function. Distinct subgroups from T lymphocytes, such as Th17, adopt specific metabolic programmes to support their needs. Some important metabolic reactions, such as glycolysis, oxidative phosphorylation, are considered important for the differentiation of these lymphocytes. Since their discovery nearly a decade ago, Th17 lymphocytes have received significant attention because of their role in the pathology of several immune-mediated inflammatory diseases such as multiple sclerosis. In this review, it will be discussed as the involvement of T cell metabolism and as metabolic reprogramming in activated T cells dictates fate decisions to Th17. The involvement of nuclear receptors such as RORyt e PPARs in the induction of Th17 cells was also discussed. Understanding the metabolic pathways involved in the differentiation of the distinct subgroups of T lymphocytes helps in the design of promising therapeutic proposals. (AU)

FAPESP's process: 17/21363-5 - Regulation of JAK/STAT/SOCS in the ontogen of IFNg-producing cells derivated from encephalitogenic Th17 cells during the clinical evolution of experimental autoimmune encephalomyelitis
Grantee:Alessandro dos Santos Farias
Support Opportunities: Regular Research Grants