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Injury-Induced Cellular Plasticity Drives Intestinal Regeneration

The epithelial lining of the intestine, particularly the stem cell compartment, is affected by harsh conditions in the luminal environment and also is susceptible to genotoxic agents such as radiation and chemotherapy. Therefore, the ability for intestinal epithelial cells to revert to a stem cell s...

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Detalles Bibliográficos
Autores principales: Meyer, Anne R., Brown, Monica E., McGrath, Patrick S., Dempsey, Peter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803615/
https://www.ncbi.nlm.nih.gov/pubmed/34915204
http://dx.doi.org/10.1016/j.jcmgh.2021.12.005
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author Meyer, Anne R.
Brown, Monica E.
McGrath, Patrick S.
Dempsey, Peter J.
author_facet Meyer, Anne R.
Brown, Monica E.
McGrath, Patrick S.
Dempsey, Peter J.
author_sort Meyer, Anne R.
collection PubMed
description The epithelial lining of the intestine, particularly the stem cell compartment, is affected by harsh conditions in the luminal environment and also is susceptible to genotoxic agents such as radiation and chemotherapy. Therefore, the ability for intestinal epithelial cells to revert to a stem cell state is an important physiological damage response to regenerate the intestinal epithelium at sites of mucosal injury. Many signaling networks involved in maintaining the stem cell niche are activated as part of the damage response to promote cellular plasticity and regeneration. The relative contribution of each cell type and signaling pathway is a critical area of ongoing research, likely dependent on the nature of injury as well as the regional specification within the intestine. Here, we review the current understanding of the multicellular cooperation to restore the intestinal epithelium after damage.
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spelling pubmed-88036152022-02-04 Injury-Induced Cellular Plasticity Drives Intestinal Regeneration Meyer, Anne R. Brown, Monica E. McGrath, Patrick S. Dempsey, Peter J. Cell Mol Gastroenterol Hepatol Original Research The epithelial lining of the intestine, particularly the stem cell compartment, is affected by harsh conditions in the luminal environment and also is susceptible to genotoxic agents such as radiation and chemotherapy. Therefore, the ability for intestinal epithelial cells to revert to a stem cell state is an important physiological damage response to regenerate the intestinal epithelium at sites of mucosal injury. Many signaling networks involved in maintaining the stem cell niche are activated as part of the damage response to promote cellular plasticity and regeneration. The relative contribution of each cell type and signaling pathway is a critical area of ongoing research, likely dependent on the nature of injury as well as the regional specification within the intestine. Here, we review the current understanding of the multicellular cooperation to restore the intestinal epithelium after damage. Elsevier 2021-12-13 /pmc/articles/PMC8803615/ /pubmed/34915204 http://dx.doi.org/10.1016/j.jcmgh.2021.12.005 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Meyer, Anne R.
Brown, Monica E.
McGrath, Patrick S.
Dempsey, Peter J.
Injury-Induced Cellular Plasticity Drives Intestinal Regeneration
title Injury-Induced Cellular Plasticity Drives Intestinal Regeneration
title_full Injury-Induced Cellular Plasticity Drives Intestinal Regeneration
title_fullStr Injury-Induced Cellular Plasticity Drives Intestinal Regeneration
title_full_unstemmed Injury-Induced Cellular Plasticity Drives Intestinal Regeneration
title_short Injury-Induced Cellular Plasticity Drives Intestinal Regeneration
title_sort injury-induced cellular plasticity drives intestinal regeneration
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803615/
https://www.ncbi.nlm.nih.gov/pubmed/34915204
http://dx.doi.org/10.1016/j.jcmgh.2021.12.005
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