IL-17 signalling is critical for controlling subcutaneous adipose tissue dynamics and parasite burden during chronic murine Trypanosoma brucei infection.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
03 11 2023
Historique:
received: 26 05 2023
accepted: 25 10 2023
medline: 6 11 2023
pubmed: 4 11 2023
entrez: 4 11 2023
Statut: epublish

Résumé

In the skin, Trypanosoma brucei colonises the subcutaneous white adipose tissue, and is proposed to be competent for forward transmission. The interaction between parasites, adipose tissue, and the local immune system is likely to drive the adipose tissue wasting and weight loss observed in cattle and humans infected with T. brucei. However, mechanistically, events leading to subcutaneous white adipose tissue wasting are not fully understood. Here, using several complementary approaches, including mass cytometry by time of flight, bulk and single cell transcriptomics, and in vivo genetic models, we show that T. brucei infection drives local expansion of several IL-17A-producing cells in the murine WAT, including T

Identifiants

pubmed: 37923768
doi: 10.1038/s41467-023-42918-8
pii: 10.1038/s41467-023-42918-8
pmc: PMC10624677
doi:

Substances chimiques

Interleukin-17 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

7070

Subventions

Organisme : Medical Research Council
ID : MR/W018497/1
Pays : United Kingdom
Organisme : NIDDK NIH HHS
ID : R01 DK125281
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK097441
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK127575
Pays : United States

Informations de copyright

© 2023. The Author(s).

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Auteurs

Matthew C Sinton (MC)

Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK. matthew.sinton@manchester.ac.uk.
School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK. matthew.sinton@manchester.ac.uk.
Division of Cardiovascular Science, University of Manchester, Manchester, UK. matthew.sinton@manchester.ac.uk.

Praveena R G Chandrasegaran (PRG)

Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK.
School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK.

Paul Capewell (P)

Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK.
School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK.

Anneli Cooper (A)

Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK.
School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK.

Alex Girard (A)

Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK.
School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK.

John Ogunsola (J)

Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK.
School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK.

Georgia Perona-Wright (G)

Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK.
School of Infection and Immunity, University of Glasgow, Glasgow, UK.

Dieudonné M Ngoyi (D)

Department of Parasitology, National Institute of Biomedical Research, Kinshasa, Democratic Republic of Congo.
Member of TrypanoGEN, Kinshasa, Democratic Republic of Congo.

Nono Kuispond (N)

Department of Parasitology, National Institute of Biomedical Research, Kinshasa, Democratic Republic of Congo.
Member of TrypanoGEN, Kinshasa, Democratic Republic of Congo.

Bruno Bucheton (B)

Member of TrypanoGEN, Kinshasa, Democratic Republic of Congo.
Institut de Recherche pour le Développement, Unité Mixte de Recherche IRD-CIRAD 177, Campus International de Baillarguet, Montpellier, France.

Mamadou Camara (M)

Member of TrypanoGEN, Kinshasa, Democratic Republic of Congo.
Programme National de Lutte contre la Trypanosomiase Humaine Africaine, Ministère de la Santé, Conakry, Guinea.

Shingo Kajimura (S)

Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Howard Hughes Medical Institute, Chevy Chase, MD, USA.

Cécile Bénézech (C)

Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, EH16 4TJ, Scotland, UK.

Neil A Mabbott (NA)

The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, UK.

Annette MacLeod (A)

Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK.
School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK.
School of Infection and Immunity, University of Glasgow, Glasgow, UK.
Member of TrypanoGEN, Kinshasa, Democratic Republic of Congo.

Juan F Quintana (JF)

Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK. juan.quintana@manchester.ac.uk.
School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK. juan.quintana@manchester.ac.uk.
Lydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, UK. juan.quintana@manchester.ac.uk.
Division of Immunology, Immunity to Infection and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK. juan.quintana@manchester.ac.uk.

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