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The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis

Kupffer cells (KCs) are the resident macrophages of the liver with similar origins to myeloid-derived macrophages. Once differentiated, KCs exhibit distinct cellular machinery capable of longevity and self-renewal, making them a crucial player in promoting effective intrahepatic communication. Howev...

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Detalles Bibliográficos
Autores principales: Zahr, Tarik, Sun, Kevin, Qiang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10388795/
https://www.ncbi.nlm.nih.gov/pubmed/37724329
http://dx.doi.org/10.1515/mr-2022-0023
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author Zahr, Tarik
Sun, Kevin
Qiang, Li
author_facet Zahr, Tarik
Sun, Kevin
Qiang, Li
author_sort Zahr, Tarik
collection PubMed
description Kupffer cells (KCs) are the resident macrophages of the liver with similar origins to myeloid-derived macrophages. Once differentiated, KCs exhibit distinct cellular machinery capable of longevity and self-renewal, making them a crucial player in promoting effective intrahepatic communication. However, this gets compromised in disease states like Nonalcoholic Steatohepatitis (NASH), where the loss of embryo-derived KCs (EmKCs) is observed. Despite this, other KC-like and KC-derived populations start to form and contribute to a variety of roles in NASH pathogenesis, often adopting a NASH-associated molecular signature. Here we offer a brief overview of recent reports describing KC polarization and reprogramming in the liver. We describe the complexities of KC cellular identity, their proposed ability to reprogram to fibroblast-like and endothelial-like cells, and the potential implications in NASH.
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spelling pubmed-103887952023-09-18 The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis Zahr, Tarik Sun, Kevin Qiang, Li Med Rev (Berl) Perspective Kupffer cells (KCs) are the resident macrophages of the liver with similar origins to myeloid-derived macrophages. Once differentiated, KCs exhibit distinct cellular machinery capable of longevity and self-renewal, making them a crucial player in promoting effective intrahepatic communication. However, this gets compromised in disease states like Nonalcoholic Steatohepatitis (NASH), where the loss of embryo-derived KCs (EmKCs) is observed. Despite this, other KC-like and KC-derived populations start to form and contribute to a variety of roles in NASH pathogenesis, often adopting a NASH-associated molecular signature. Here we offer a brief overview of recent reports describing KC polarization and reprogramming in the liver. We describe the complexities of KC cellular identity, their proposed ability to reprogram to fibroblast-like and endothelial-like cells, and the potential implications in NASH. De Gruyter 2022-09-20 /pmc/articles/PMC10388795/ /pubmed/37724329 http://dx.doi.org/10.1515/mr-2022-0023 Text en © 2022 the author(s), published by De Gruyter, Berlin/Boston https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Perspective
Zahr, Tarik
Sun, Kevin
Qiang, Li
The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis
title The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis
title_full The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis
title_fullStr The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis
title_full_unstemmed The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis
title_short The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis
title_sort polarizable and reprogrammable identity of kupffer cells in nonalcoholic steatohepatitis
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10388795/
https://www.ncbi.nlm.nih.gov/pubmed/37724329
http://dx.doi.org/10.1515/mr-2022-0023
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