A cell-based drug delivery platform for treating central nervous system inflammation.
Animals
Cell Proliferation
/ drug effects
Drug Delivery Systems
/ methods
Drug Liberation
Encephalomyelitis, Autoimmune, Experimental
/ blood
Enzyme Inhibitors
/ administration & dosage
Female
Humans
Immunity
/ drug effects
Indoles
/ administration & dosage
Maleimides
/ administration & dosage
Mesenchymal Stem Cells
/ drug effects
Mice
Mice, Inbred C57BL
Multiple Sclerosis
/ blood
T-Lymphocytes
/ drug effects
Tissue Distribution
Transplantation, Heterologous
/ methods
Treatment Outcome
Drug delivery
Mesenchymal stem cells
Multiple sclerosis
Ro-31-8425
Journal
Journal of molecular medicine (Berlin, Germany)
ISSN: 1432-1440
Titre abrégé: J Mol Med (Berl)
Pays: Germany
ID NLM: 9504370
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
received:
16
06
2020
accepted:
29
10
2020
revised:
22
10
2020
pubmed:
6
1
2021
medline:
29
1
2022
entrez:
5
1
2021
Statut:
ppublish
Résumé
Mesenchymal stem cells (MSCs) are promising candidates for the development of cell-based drug delivery systems for autoimmune inflammatory diseases, such as multiple sclerosis (MS). Here, we investigated the effect of Ro-31-8425, an ATP-competitive kinase inhibitor, on the therapeutic properties of MSCs. Upon a simple pretreatment procedure, MSCs spontaneously took up and then gradually released significant amounts of Ro-31-8425. Ro-31-8425 (free or released by MSCs) suppressed the proliferation of CD4
Identifiants
pubmed: 33398468
doi: 10.1007/s00109-020-02003-9
pii: 10.1007/s00109-020-02003-9
pmc: PMC8292974
mid: NIHMS1720293
doi:
Substances chimiques
Enzyme Inhibitors
0
Indoles
0
Maleimides
0
Ro 31-8425
131848-97-0
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
663-671Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL095722
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS102807
Pays : United States
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