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Dissecting Alzheimer's disease pathogenesis in human 2D and 3D models.
Cenini, Giovanna; Hebisch, Matthias; Iefremova, Vira; Flitsch, Lea J; Breitkreuz, Yannik; Tanzi, Rudolph E; Kim, Doo Yeon; Peitz, Michael; Brüstle, Oliver.
Afiliação
  • Cenini G; Institute of Reconstructive Neurobiology, University of Bonn Medical Faculty & University Hospital Bonn, Venusberg-Campus 1, D-53127 Bonn, Germany.
  • Hebisch M; Genetics and Aging Research Unit, MassGeneral Institute for Neurodegenerative Disease, Department of Neurology, McCance Center for Brain Health, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.
  • Iefremova V; Institute of Reconstructive Neurobiology, University of Bonn Medical Faculty & University Hospital Bonn, Venusberg-Campus 1, D-53127 Bonn, Germany.
  • Flitsch LJ; Institute of Reconstructive Neurobiology, University of Bonn Medical Faculty & University Hospital Bonn, Venusberg-Campus 1, D-53127 Bonn, Germany.
  • Breitkreuz Y; Institute of Reconstructive Neurobiology, University of Bonn Medical Faculty & University Hospital Bonn, Venusberg-Campus 1, D-53127 Bonn, Germany; LIFE & BRAIN GmbH, Cellomics Unit, Venusberg-Campus 1, D-53127 Bonn, Germany.
  • Tanzi RE; Genetics and Aging Research Unit, MassGeneral Institute for Neurodegenerative Disease, Department of Neurology, McCance Center for Brain Health, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.
  • Kim DY; Genetics and Aging Research Unit, MassGeneral Institute for Neurodegenerative Disease, Department of Neurology, McCance Center for Brain Health, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.
  • Peitz M; Institute of Reconstructive Neurobiology, University of Bonn Medical Faculty & University Hospital Bonn, Venusberg-Campus 1, D-53127 Bonn, Germany; Cell Programming Core Facility, University of Bonn Medical Faculty & University Hospital Bonn, Venusberg-Campus 1, D-53127 Bonn, Germany.
  • Brüstle O; Institute of Reconstructive Neurobiology, University of Bonn Medical Faculty & University Hospital Bonn, Venusberg-Campus 1, D-53127 Bonn, Germany. Electronic address: brustle@uni-bonn.de.
Mol Cell Neurosci ; 110: 103568, 2021 01.
Article em En | MEDLINE | ID: mdl-33068718
ABSTRACT
The incidence of Alzheimer's disease is increasing with the aging population, and it has become one of the main health concerns of modern society. The dissection of the underlying pathogenic mechanisms and the development of effective therapies remain extremely challenging, also because available animal and cell culture models do not fully recapitulate the whole spectrum of pathological changes. The advent of human pluripotent stem cells and cell reprogramming has provided new prospects for tackling these challenges in a human and even patient-specific setting. Yet, experimental modeling of non-cell autonomous and extracellular disease-related alterations has remained largely inaccessible. These limitations are about to be overcome by advances in the development of 3D cell culture systems including organoids, neurospheroids and matrix-embedded 3D cultures, which have been shown to recapitulate extracellular pathologies such as plaque formation in vitro. Recent xenograft studies have even taken human stem cell-based disease modeling to an in vivo scenario where grafted neurons are probed in a disease background in the context of a rodent brain. Here, we review the latest developments in this emerging field along with their advantages, challenges, and future prospects.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Medicina de Precisão / Doença de Alzheimer / Cultura Primária de Células Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Medicina de Precisão / Doença de Alzheimer / Cultura Primária de Células Idioma: En Ano de publicação: 2021 Tipo de documento: Article