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Hematopoiesis of Indeterminate Potential and Atherothrombotic Risk
Hematopoiesis is the process of blood production, essential for the continued supply of immune cells and red blood cells. However, the proliferative nature of hematopoietic stem cells (HSCs) renders them susceptible to developing somatic mutations. HSCs carrying a mutation can gain a selective advan...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Georg Thieme Verlag KG
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420552/ https://www.ncbi.nlm.nih.gov/pubmed/35445383 http://dx.doi.org/10.1055/a-1830-2147 |
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author | Murphy, Andrew J. Dragoljevic, Dragana Natarajan, Pradeep Wang, Nan |
author_facet | Murphy, Andrew J. Dragoljevic, Dragana Natarajan, Pradeep Wang, Nan |
author_sort | Murphy, Andrew J. |
collection | PubMed |
description | Hematopoiesis is the process of blood production, essential for the continued supply of immune cells and red blood cells. However, the proliferative nature of hematopoietic stem cells (HSCs) renders them susceptible to developing somatic mutations. HSCs carrying a mutation can gain a selective advantage over normal HSCs and result in hematological disorders. One such disorder is termed clonal hematopoiesis of indeterminate potential (CHIP), a premalignant state associated with aging, where the mutant HSCs are responsible for producing a small portion of mature immune cells in the circulation and subsequently in tissues. People with CHIP have been shown to have an increased risk of mortality due to cardiovascular disease (CVD). Why this occurs is under rigorous investigation, but the majority of the studies to date have suggested that increased atherosclerosis is due to heightened inflammatory cytokine release from mutant lesional macrophages. However, given CHIP is driven by several mutations, other hematopoietic lineages can be altered to promote CVD. In this review we explore the relationship between mutations in genes causing CHIP and atherothrombotic disorders, along with potential mechanisms of enhanced clonal outgrowth and potential therapies and strategies to slow CHIP progression. |
format | Online Article Text |
id | pubmed-9420552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-94205522022-08-29 Hematopoiesis of Indeterminate Potential and Atherothrombotic Risk Murphy, Andrew J. Dragoljevic, Dragana Natarajan, Pradeep Wang, Nan Thromb Haemost Hematopoiesis is the process of blood production, essential for the continued supply of immune cells and red blood cells. However, the proliferative nature of hematopoietic stem cells (HSCs) renders them susceptible to developing somatic mutations. HSCs carrying a mutation can gain a selective advantage over normal HSCs and result in hematological disorders. One such disorder is termed clonal hematopoiesis of indeterminate potential (CHIP), a premalignant state associated with aging, where the mutant HSCs are responsible for producing a small portion of mature immune cells in the circulation and subsequently in tissues. People with CHIP have been shown to have an increased risk of mortality due to cardiovascular disease (CVD). Why this occurs is under rigorous investigation, but the majority of the studies to date have suggested that increased atherosclerosis is due to heightened inflammatory cytokine release from mutant lesional macrophages. However, given CHIP is driven by several mutations, other hematopoietic lineages can be altered to promote CVD. In this review we explore the relationship between mutations in genes causing CHIP and atherothrombotic disorders, along with potential mechanisms of enhanced clonal outgrowth and potential therapies and strategies to slow CHIP progression. Georg Thieme Verlag KG 2022-06-18 /pmc/articles/PMC9420552/ /pubmed/35445383 http://dx.doi.org/10.1055/a-1830-2147 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Murphy, Andrew J. Dragoljevic, Dragana Natarajan, Pradeep Wang, Nan Hematopoiesis of Indeterminate Potential and Atherothrombotic Risk |
title | Hematopoiesis of Indeterminate Potential and Atherothrombotic Risk |
title_full | Hematopoiesis of Indeterminate Potential and Atherothrombotic Risk |
title_fullStr | Hematopoiesis of Indeterminate Potential and Atherothrombotic Risk |
title_full_unstemmed | Hematopoiesis of Indeterminate Potential and Atherothrombotic Risk |
title_short | Hematopoiesis of Indeterminate Potential and Atherothrombotic Risk |
title_sort | hematopoiesis of indeterminate potential and atherothrombotic risk |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420552/ https://www.ncbi.nlm.nih.gov/pubmed/35445383 http://dx.doi.org/10.1055/a-1830-2147 |
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