Alegre 2019 Am J Transplant: Difference between revisions

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{{Template:Correction FADH2 and S-pathway}}
{{Template:Correction FADH2 and S-pathway}}

Latest revision as of 21:37, 22 October 2023

Publications in the MiPMap
Alegre ML (2019) Treg respiration. Am J Transplant 19:969. https://doi.org/10.1111/ajt.15334.

Β» Am J Transplant Open Access

Alegre ML (2019) Am J Transplant

Abstract: Literature Watch 969 BY MARIA-LUISA ALEGRE, MD, PHD Regulatory T cells that express the transcription factor FoxP3 (Tregs) are essential for the maintenance of immune homeostasis. A lack of Tregs at birth, Treg deletion in adulthood or the selective ablation of the T cell receptor (TCR) in Tregs or of key membrane-associated or signaling molecules, such as CTLA-4, CD28 or PTEN, have been shown in mice to lead to dramatic lymphoproliferative disease, tissue infiltration by activated conventional T cells (Tconvs) and, in many cases, animal death. This underscores the importance of continuous and proper activation of Tregs throughout life. Tregs have a unique metabolic profile, including greater mitochondrial metabolism than Tconvs. Weinberg and colleagues investigate whether mitochondrial respiration (Figure 1) is necessary for the ability of Tregs to maintain homeostasis, and find that tampering with Treg–mitochondrial complex III triggers fatal autoimmunity.

β€’ Bioblast editor: Gnaiger E

Alegre 2019 Am J Transplant CORRECTION.png

Correction: FADH2 and Complex II

Ambiguity alert.png
FADH2 is shown as the substrate feeding electrons into Complex II (CII). This is wrong and requires correction - for details see Gnaiger (2024).
Gnaiger E (2024) Complex II ambiguities ― FADH2 in the electron transfer system. J Biol Chem 300:105470. https://doi.org/10.1016/j.jbc.2023.105470 - Β»Bioblast linkΒ«
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