Novel human iPSC models of neuroinflammation in neurodegenerative disease and regenerative medicine.

Alzheimer’s disease Parkinson’s disease cell differentiation glia hiPSC microglia multiple sclerosis neuroinflammation organoids

Journal

Trends in immunology
ISSN: 1471-4981
Titre abrégé: Trends Immunol
Pays: England
ID NLM: 100966032

Informations de publication

Date de publication:
21 Sep 2024
Historique:
received: 27 07 2024
revised: 23 08 2024
accepted: 25 08 2024
medline: 23 9 2024
pubmed: 23 9 2024
entrez: 22 9 2024
Statut: aheadofprint

Résumé

The importance of neuroinflammation in neurodegenerative diseases is becoming increasingly evident, and, in parallel, human induced pluripotent stem cell (hiPSC) models of physiology and pathology are emerging. Here, we review new advancements in the differentiation of hiPSCs into glial, neural, and blood-brain barrier (BBB) cell types, and the integration of these cells into complex organoids and chimeras. These advancements are relevant for modeling neuroinflammation in the context of prevalent neurodegenerative disorders, such as Alzheimer's disease (AD), Parkinson's disease (PD), and multiple sclerosis (MS). With awareness of current limitations, recent progress in the development and application of various hiPSC-derived models shows potential for aiding the identification of candidate therapeutic targets and immunotherapy approaches.

Identifiants

pubmed: 39307583
pii: S1471-4906(24)00190-X
doi: 10.1016/j.it.2024.08.004
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of interests M.A. has received consultancy and/or speaker honoraria from Abata Therapeutics, Biogen, Sanofi, Immunic Therapeutics, and GSK. D.S.R. has received research funding from Abata Therapeutics and Sanofi. The other authors have nothing to disclose.

Auteurs

Rose Ana Summers (RA)

Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK; Translational Neuroradiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Francesca Fagiani (F)

Translational Neuropathology Unit, Institute of Experimental Neurology, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.

David H Rowitch (DH)

Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

Martina Absinta (M)

Translational Neuropathology Unit, Institute of Experimental Neurology, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Daniel S Reich (DS)

Translational Neuroradiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA. Electronic address: daniel.reich@nih.gov.

Classifications MeSH