Human liver derived mesenchymal stromal cells ameliorate murine ischemia-induced inflammation through macrophage polarization.
immunomodulation
inflammation
liver tolerance
mesenchymal stromal cells
renal artery stenosis
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2024
2024
Historique:
received:
12
06
2024
accepted:
04
07
2024
medline:
6
8
2024
pubmed:
6
8
2024
entrez:
6
8
2024
Statut:
epublish
Résumé
The immunomodulatory properties of mesenchymal stromal cells (MSC) have been well-characterized in To test these observations The stenotic kidney volume was smaller in all RAS mice, confirming significant injury, and was improved by infusion of all MSC types. All MSC-infused groups had lower levels of plasma renin and proteinuria compared to untreated RAS. Serum creatinine improved in micetreated with BM- and L-MSC. All types of MSC located to and were retained within the stenotic kidneys, but L-MSC retention was significantly higher than A- and BM-MSC. While all groups of MSC-treated mice displayed reduced overall inflammation and macrophage counts, L-MSC showed superior potency These
Identifiants
pubmed: 39104523
doi: 10.3389/fimmu.2024.1448092
pmc: PMC11298378
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1448092Informations de copyright
Copyright © 2024 Liang, Ozdogan, Hansen, Tang, Saadiq, Jordan, Krier, Gandhi, Grande, Lerman and Taner.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.