Sexual Dimorphism in the Polarization of Cardiac ILCs through Elabela.

CD28 Elabela ILCs cardiac ILCs heart immunity innate immunity sexual-dimorphism

Journal

Current issues in molecular biology
ISSN: 1467-3045
Titre abrégé: Curr Issues Mol Biol
Pays: Switzerland
ID NLM: 100931761

Informations de publication

Date de publication:
30 Dec 2022
Historique:
received: 30 09 2022
revised: 16 12 2022
accepted: 23 12 2022
entrez: 20 1 2023
pubmed: 21 1 2023
medline: 21 1 2023
Statut: epublish

Résumé

Elabela is a component of the apelinergic system and may exert a cardioprotective role by regulating the innate immune responses. Innate lymphoid cells (ILCs) have a significant role in initiating and progressing immune-inflammatory responses. While ILCs have been intensively investigated during the last decade, little is known about their relationship with the apelinergic system and their cardiac diversity in a gender-based paradigm. In this study, we investigated the polarization of cardiac ILCs by Elabela in males versus females in a mouse model. Using flow cytometry and immunohistochemistry analyses, we showed a potential interplay between Elabela and cardiac ILCs and whether such interactions depend on sexual dimorphism. Our findings showed, for the first time, that Elabela is expressed by cardiac ILCs, and its expression is higher in females' ILC class 3 (ILC3s) compared to males. Females had higher frequencies of ILC1s, and Elabela was able to suppress T-cell activation and the expression of co-stimulatory CD28 in a mixed lymphocyte reaction assay (MLR). In conclusion, our results suggest, for the first time, a protective role for Elabela through its interplay with ILCs and that it can be used as an immunotherapeutic target in the treatment of cardiovascular disorders in a gender-based fashion.

Identifiants

pubmed: 36661503
pii: cimb45010017
doi: 10.3390/cimb45010017
pmc: PMC9856941
doi:

Types de publication

Journal Article

Langues

eng

Pagination

223-232

Subventions

Organisme : National Institute of Health
ID : NS110378

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Auteurs

Évila Lopes Salles (ÉL)

Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

Sahar Emami Naeini (S)

Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

Bidhan Bhandari (B)

Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

Hesam Khodadadi (H)

Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

Edie Threlkeld (E)

Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.

Sholeh Rezaee (S)

Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.

William Meeks (W)

Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

Avery Meeks (A)

Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

Aderemi Awe (A)

Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.

Ahmed El-Marakby (A)

Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

Jack C Yu (JC)

Department of Plastic Surgery, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.

Lei P Wang (LP)

Medicinal Cannabis of Georgia LLC, Augusta, GA 30912, USA.

Babak Baban (B)

Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

Classifications MeSH