Human liver derived mesenchymal stromal cells ameliorate murine ischemia-induced inflammation through macrophage polarization.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
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

1448092

Informations 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.

Auteurs

Yun Liang (Y)

Department of Surgery, Mayo Clinic, Rochester, MN, United States.

Elif Ozdogan (E)

Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.

Michael J Hansen (MJ)

Department of Immunology, Mayo Clinic, Rochester, MN, United States.

Hui Tang (H)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States.

Ishran Saadiq (I)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States.

Kyra L Jordan (KL)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States.

James D Krier (JD)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States.

Deep B Gandhi (DB)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States.

Joseph P Grande (JP)

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States.

Lilach O Lerman (LO)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States.

Timucin Taner (T)

Department of Surgery, Mayo Clinic, Rochester, MN, United States.
Department of Immunology, Mayo Clinic, Rochester, MN, United States.

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