Soluble CD14 produced by bovine mammary epithelial cells modulates their response to full length LPS.


Journal

Veterinary research
ISSN: 1297-9716
Titre abrégé: Vet Res
Pays: England
ID NLM: 9309551

Informations de publication

Date de publication:
12 Jun 2024
Historique:
received: 12 09 2023
accepted: 04 05 2024
medline: 13 6 2024
pubmed: 13 6 2024
entrez: 12 6 2024
Statut: epublish

Résumé

Bovine mastitis remains a major disease in cattle world-wide. In the mammary gland, mammary epithelial cells (MEC) are sentinels equipped with receptors allowing them to detect and respond to the invasion by bacterial pathogens, in particular Escherichia coli. Lipopolysaccharide (LPS) is the major E. coli motif recognized by MEC through its interaction with the TLR4 receptor and the CD14 co-receptor. Previous studies have highlighted the role of soluble CD14 (sCD14) in the efficient recognition of LPS molecules possessing a full-length O-antigen (LPSS). We demonstrate here that MEC are able to secrete CD14 and are likely to contribute to the presence of sCD14 in milk. We then investigated how sCD14 modulates and is required for the response of MEC to LPSS. This study highlights the key role of sCD14 for the full activation of the Myd88-independent pathway by LPSS. We also identified several lncRNA that are activated in MEC in response to LPS, including one lncRNA showing homologies with the mir-99a-let-7c gene (MIR99AHG). Altogether, our results show that a full response to LPS by mammary epithelial cells requires sCD14 and provide detailed information on how milk sCD14 can contribute to an efficient recognition of LPS from coliform pathogens.

Identifiants

pubmed: 38867337
doi: 10.1186/s13567-024-01329-3
pii: 10.1186/s13567-024-01329-3
doi:

Substances chimiques

Lipopolysaccharide Receptors 0
Lipopolysaccharides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

76

Informations de copyright

© 2024. The Author(s).

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Auteurs

Mégane Védrine (M)

ISP UMR 1282, INRAE, Université François Rabelais de Tours, Nouzilly, France.

Florence B Gilbert (FB)

ISP UMR 1282, INRAE, Université François Rabelais de Tours, Nouzilly, France.

Sarah Maman (S)

SIGENAE, GenPhySE, Université de Toulouse, INRAE, INPT, ENVT, 31326, Castanet Tolosan, France.

Christophe Klopp (C)

SIGENAE, Genotoul Bioinfo, BioInfoMics, MIAT UR875, INRAE, Castanet Tolosan, France.

Christophe Gitton (C)

ISP UMR 1282, INRAE, Université François Rabelais de Tours, Nouzilly, France.

Pascal Rainard (P)

ISP UMR 1282, INRAE, Université François Rabelais de Tours, Nouzilly, France.

Pierre Germon (P)

ISP UMR 1282, INRAE, Université François Rabelais de Tours, Nouzilly, France. pierre.germon@inrae.fr.

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