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Mechanistic and Translational Advances Using iPSC-Derived Blood Cells

Human induced pluripotent stem cell (iPSC)-based model systems can be used to produce blood cells for the study of both hematologic and non-hematologic disorders. This commentary discusses recent advances that have utilized iPSC-derived red blood cells, megakaryocytes, myeloid cells, and lymphoid ce...

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Autores principales: Thom, Christopher S, Chou, Stella T, French, Deborah L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990314/
https://www.ncbi.nlm.nih.gov/pubmed/33768218
http://dx.doi.org/10.33696/pathology.1.010
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author Thom, Christopher S
Chou, Stella T
French, Deborah L
author_facet Thom, Christopher S
Chou, Stella T
French, Deborah L
author_sort Thom, Christopher S
collection PubMed
description Human induced pluripotent stem cell (iPSC)-based model systems can be used to produce blood cells for the study of both hematologic and non-hematologic disorders. This commentary discusses recent advances that have utilized iPSC-derived red blood cells, megakaryocytes, myeloid cells, and lymphoid cells to model hematopoietic disorders. In addition, we review recent studies that have defined how microglial cells differentiated from iPSC-derived monocytes impact neurodegenerative disease. Related translational insights highlight the utility of iPSC models for studying pathologic anemia, bleeding, thrombosis, autoimmunity, immunodeficiency, blood cancers, and neurodegenerative disease such as Alzheimer’s.
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spelling pubmed-79903142021-03-24 Mechanistic and Translational Advances Using iPSC-Derived Blood Cells Thom, Christopher S Chou, Stella T French, Deborah L J Exp Pathol (Wilmington) Article Human induced pluripotent stem cell (iPSC)-based model systems can be used to produce blood cells for the study of both hematologic and non-hematologic disorders. This commentary discusses recent advances that have utilized iPSC-derived red blood cells, megakaryocytes, myeloid cells, and lymphoid cells to model hematopoietic disorders. In addition, we review recent studies that have defined how microglial cells differentiated from iPSC-derived monocytes impact neurodegenerative disease. Related translational insights highlight the utility of iPSC models for studying pathologic anemia, bleeding, thrombosis, autoimmunity, immunodeficiency, blood cancers, and neurodegenerative disease such as Alzheimer’s. 2020 /pmc/articles/PMC7990314/ /pubmed/33768218 http://dx.doi.org/10.33696/pathology.1.010 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Thom, Christopher S
Chou, Stella T
French, Deborah L
Mechanistic and Translational Advances Using iPSC-Derived Blood Cells
title Mechanistic and Translational Advances Using iPSC-Derived Blood Cells
title_full Mechanistic and Translational Advances Using iPSC-Derived Blood Cells
title_fullStr Mechanistic and Translational Advances Using iPSC-Derived Blood Cells
title_full_unstemmed Mechanistic and Translational Advances Using iPSC-Derived Blood Cells
title_short Mechanistic and Translational Advances Using iPSC-Derived Blood Cells
title_sort mechanistic and translational advances using ipsc-derived blood cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990314/
https://www.ncbi.nlm.nih.gov/pubmed/33768218
http://dx.doi.org/10.33696/pathology.1.010
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