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Thioredoxin is a metabolic rheostat controlling regulatory B cells

Title: Thioredoxin is a metabolic rheostat controlling regulatory B cells
Authors: Bradford, HF; McDonnell, TCR; Stewart, A; Skelton, A; Ng, J; Baig, Z; Fraternali, F; Dunn-Walters, D; Isenberg, DA; Khan, AR; Mauro, C; Mauri, C
Source: Nature Immunology (2024) (In press).
Publisher Information: Springer Science and Business Media LLC
Publication Year: 2024
Collection: University College London: UCL Discovery
Subject Terms: Autoimmunity; B cells; Biochemistry; Pathogenesis
Description: Metabolic programming is important for B cell fate, but the bioenergetic requirement for regulatory B (Breg) cell differentiation and function is unknown. Here we show that Breg cell differentiation, unlike non-Breg cells, relies on mitochondrial electron transport and homeostatic levels of reactive oxygen species (ROS). Single-cell RNA sequencing analysis revealed that TXN, encoding the metabolic redox protein thioredoxin (Trx), is highly expressed by Breg cells, unlike Trx inhibitor TXNIP which was downregulated. Pharmacological inhibition or gene silencing of TXN resulted in mitochondrial membrane depolarization and increased ROS levels, selectively suppressing Breg cell differentiation and function while favoring pro-inflammatory B cell differentiation. Patients with systemic lupus erythematosus (SLE), characterized by Breg cell deficiencies, present with B cell mitochondrial membrane depolarization, elevated ROS and fewer Trx+ B cells. Exogenous Trx stimulation restored Breg cells and mitochondrial membrane polarization in SLE B cells to healthy B cell levels, indicating Trx insufficiency underlies Breg cell impairment in patients with SLE.
Document Type: article in journal/newspaper
File Description: text
Language: English
Relation: https://discovery.ucl.ac.uk/id/eprint/10190311/
Availability: https://discovery.ucl.ac.uk/id/eprint/10190311/1/s41590-024-01798-w.pdf; https://discovery.ucl.ac.uk/id/eprint/10190311/
Rights: open
Accession Number: edsbas.F4CBB9F1
Database: BASE