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Zebrafish models of inflammation in hematopoietic development and disease
Zebrafish offer an excellent tool for studying the vertebrate hematopoietic system thanks to a highly conserved and rapidly developing hematopoietic program, genetic amenability, optical transparency, and experimental accessibility. Zebrafish studies have contributed to our understanding of hematopo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340492/ https://www.ncbi.nlm.nih.gov/pubmed/35923854 http://dx.doi.org/10.3389/fcell.2022.955658 |
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author | Ketharnathan, Sarada Rajan, Vinothkumar Prykhozhij, Sergey V. Berman, Jason N. |
author_facet | Ketharnathan, Sarada Rajan, Vinothkumar Prykhozhij, Sergey V. Berman, Jason N. |
author_sort | Ketharnathan, Sarada |
collection | PubMed |
description | Zebrafish offer an excellent tool for studying the vertebrate hematopoietic system thanks to a highly conserved and rapidly developing hematopoietic program, genetic amenability, optical transparency, and experimental accessibility. Zebrafish studies have contributed to our understanding of hematopoiesis, a complex process regulated by signaling cues, inflammation being crucial among them. Hematopoietic stem cells (HSCs) are multipotent cells producing all the functional blood cells, including immune cells. HSCs respond to inflammation during infection and malignancy by proliferating and producing the blood cells in demand for a specific scenario. We first focus on how inflammation plays a crucial part in steady-state HSC development and describe the critical role of the inflammasome complex in regulating HSC expansion and balanced lineage production. Next, we review zebrafish studies of inflammatory innate immune mechanisms focusing on interferon signaling and the downstream JAK-STAT pathway. We also highlight insights gained from zebrafish models harbouring genetic perturbations in the role of inflammation in hematopoietic disorders such as bone marrow failure, myelodysplastic syndrome, and myeloid leukemia. Indeed, inflammation has been recently identified as a potential driver of clonal hematopoiesis and leukemogenesis, where cells acquire somatic mutations that provide a proliferative advantage in the presence of inflammation. Important insights in this area come from mutant zebrafish studies showing that hematopoietic differentiation can be compromised by epigenetic dysregulation and the aberrant induction of signaling pathways. |
format | Online Article Text |
id | pubmed-9340492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93404922022-08-02 Zebrafish models of inflammation in hematopoietic development and disease Ketharnathan, Sarada Rajan, Vinothkumar Prykhozhij, Sergey V. Berman, Jason N. Front Cell Dev Biol Cell and Developmental Biology Zebrafish offer an excellent tool for studying the vertebrate hematopoietic system thanks to a highly conserved and rapidly developing hematopoietic program, genetic amenability, optical transparency, and experimental accessibility. Zebrafish studies have contributed to our understanding of hematopoiesis, a complex process regulated by signaling cues, inflammation being crucial among them. Hematopoietic stem cells (HSCs) are multipotent cells producing all the functional blood cells, including immune cells. HSCs respond to inflammation during infection and malignancy by proliferating and producing the blood cells in demand for a specific scenario. We first focus on how inflammation plays a crucial part in steady-state HSC development and describe the critical role of the inflammasome complex in regulating HSC expansion and balanced lineage production. Next, we review zebrafish studies of inflammatory innate immune mechanisms focusing on interferon signaling and the downstream JAK-STAT pathway. We also highlight insights gained from zebrafish models harbouring genetic perturbations in the role of inflammation in hematopoietic disorders such as bone marrow failure, myelodysplastic syndrome, and myeloid leukemia. Indeed, inflammation has been recently identified as a potential driver of clonal hematopoiesis and leukemogenesis, where cells acquire somatic mutations that provide a proliferative advantage in the presence of inflammation. Important insights in this area come from mutant zebrafish studies showing that hematopoietic differentiation can be compromised by epigenetic dysregulation and the aberrant induction of signaling pathways. Frontiers Media S.A. 2022-07-18 /pmc/articles/PMC9340492/ /pubmed/35923854 http://dx.doi.org/10.3389/fcell.2022.955658 Text en Copyright © 2022 Ketharnathan, Rajan, Prykhozhij and Berman. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Ketharnathan, Sarada Rajan, Vinothkumar Prykhozhij, Sergey V. Berman, Jason N. Zebrafish models of inflammation in hematopoietic development and disease |
title | Zebrafish models of inflammation in hematopoietic development and disease |
title_full | Zebrafish models of inflammation in hematopoietic development and disease |
title_fullStr | Zebrafish models of inflammation in hematopoietic development and disease |
title_full_unstemmed | Zebrafish models of inflammation in hematopoietic development and disease |
title_short | Zebrafish models of inflammation in hematopoietic development and disease |
title_sort | zebrafish models of inflammation in hematopoietic development and disease |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340492/ https://www.ncbi.nlm.nih.gov/pubmed/35923854 http://dx.doi.org/10.3389/fcell.2022.955658 |
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