Journal

ACS applied materials & interfaces
ISSN: 1944-8252
Titre abrégé: ACS Appl Mater Interfaces
Pays: United States
ID NLM: 101504991

Informations de publication

Date de publication:
26 May 2021
Historique:
pubmed: 13 5 2021
medline: 24 8 2021
entrez: 12 5 2021
Statut: ppublish

Résumé

Transplanted glial-restricted progenitor (GRP) cells have potential to focally replace defunct astrocytes and produce remyelinating oligodendrocytes to avert neuronal death and dysfunction. However, most central nervous system cell therapeutic paradigms are hampered by high initial cell death and a host anti-graft immune response. We show here that composite hyaluronic acid-based hydrogels of tunable mechanical strengths can significantly improve transplanted GRP survival and differentiation. Allogeneic GRPs expressing green fluorescent protein and firefly luciferase were scaffolded in optimized hydrogel formulations and transplanted intracerebrally into immunocompetent BALB/c mice followed by serial

Identifiants

pubmed: 33978398
doi: 10.1021/acsami.1c03415
pmc: PMC9440547
mid: NIHMS1832114
doi:

Substances chimiques

Hydrogels 0
Hyaluronic Acid 9004-61-9

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

23423-23437

Subventions

Organisme : NIBIB NIH HHS
ID : R01 EB023647
Pays : United States
Organisme : NIBIB NIH HHS
ID : R21 EB026711
Pays : United States
Organisme : NIH HHS
ID : S10 OD010744
Pays : United States

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Auteurs

Shreyas Kuddannaya (S)

The Russell H. Morgan Department of Radiology and Radiological Science, Division of MR Research, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.
Cellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.

Wei Zhu (W)

The Russell H. Morgan Department of Radiology and Radiological Science, Division of MR Research, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.
Cellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.

Chengyan Chu (C)

The Russell H. Morgan Department of Radiology and Radiological Science, Division of MR Research, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.
Cellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.

Anirudha Singh (A)

Department of Urology, the James Buchanan Brady Urological Institute, The Johns Hopkins School of Medicine, Baltimore, Maryland 21287, United States.
Department of Chemical & Biomolecular Engineering, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.

Piotr Walczak (P)

Center for Advanced Imaging Research, Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland, Baltimore, Maryland 21201, United States.

Jeff W M Bulte (JWM)

The Russell H. Morgan Department of Radiology and Radiological Science, Division of MR Research, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.
Cellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.
Department of Chemical & Biomolecular Engineering, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.
Department of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, United States.
Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, United States.

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Classifications MeSH