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Fetal liver hematopoiesis: from development to delivery

Clinical transplants of hematopoietic stem cells (HSC) can provide a lifesaving therapy for many hematological diseases; however, therapeutic applications are hampered by donor availability. In vivo, HSC exist in a specified microenvironment called the niche. While most studies of the niche focus on...

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Autores principales: Lewis, Kyle, Yoshimoto, Momoko, Takebe, Takanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890853/
https://www.ncbi.nlm.nih.gov/pubmed/33597015
http://dx.doi.org/10.1186/s13287-021-02189-w
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author Lewis, Kyle
Yoshimoto, Momoko
Takebe, Takanori
author_facet Lewis, Kyle
Yoshimoto, Momoko
Takebe, Takanori
author_sort Lewis, Kyle
collection PubMed
description Clinical transplants of hematopoietic stem cells (HSC) can provide a lifesaving therapy for many hematological diseases; however, therapeutic applications are hampered by donor availability. In vivo, HSC exist in a specified microenvironment called the niche. While most studies of the niche focus on those residing in the bone marrow (BM), a better understanding of the fetal liver niche during development is vital to design human pluripotent stem cell (PSC) culture and may provide valuable insights with regard to expanding HSCs ex vivo for transplantation. This review will discuss the importance of the fetal liver niche in HSC expansion, a feat that occurs during development and has great clinical potential. We will also discuss emerging approaches to generate expandable HSC in cell culture that attain more complexity in the form of cells or organoid models in combination with engineering and systems biology approaches. Overall, delivering HSC by charting developmental principles will help in the understanding of the molecular and biological interactions between HSCs and fetal liver cells for their controlled maturation and expansion.
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spelling pubmed-78908532021-02-22 Fetal liver hematopoiesis: from development to delivery Lewis, Kyle Yoshimoto, Momoko Takebe, Takanori Stem Cell Res Ther Review Clinical transplants of hematopoietic stem cells (HSC) can provide a lifesaving therapy for many hematological diseases; however, therapeutic applications are hampered by donor availability. In vivo, HSC exist in a specified microenvironment called the niche. While most studies of the niche focus on those residing in the bone marrow (BM), a better understanding of the fetal liver niche during development is vital to design human pluripotent stem cell (PSC) culture and may provide valuable insights with regard to expanding HSCs ex vivo for transplantation. This review will discuss the importance of the fetal liver niche in HSC expansion, a feat that occurs during development and has great clinical potential. We will also discuss emerging approaches to generate expandable HSC in cell culture that attain more complexity in the form of cells or organoid models in combination with engineering and systems biology approaches. Overall, delivering HSC by charting developmental principles will help in the understanding of the molecular and biological interactions between HSCs and fetal liver cells for their controlled maturation and expansion. BioMed Central 2021-02-17 /pmc/articles/PMC7890853/ /pubmed/33597015 http://dx.doi.org/10.1186/s13287-021-02189-w Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Lewis, Kyle
Yoshimoto, Momoko
Takebe, Takanori
Fetal liver hematopoiesis: from development to delivery
title Fetal liver hematopoiesis: from development to delivery
title_full Fetal liver hematopoiesis: from development to delivery
title_fullStr Fetal liver hematopoiesis: from development to delivery
title_full_unstemmed Fetal liver hematopoiesis: from development to delivery
title_short Fetal liver hematopoiesis: from development to delivery
title_sort fetal liver hematopoiesis: from development to delivery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890853/
https://www.ncbi.nlm.nih.gov/pubmed/33597015
http://dx.doi.org/10.1186/s13287-021-02189-w
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