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Ribosome-Induced Cellular Multipotency, an Emerging Avenue in Cell Fate Reversal

The ribosome, which is present in all three domains of life, plays a well-established, critical role in the translation process by decoding messenger RNA into protein. Ribosomal proteins, in contrast, appear to play non-translational roles in growth, differentiation, and disease. We recently discove...

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Detalles Bibliográficos
Autores principales: Istiaq, Arif, Ohta, Kunimasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469204/
https://www.ncbi.nlm.nih.gov/pubmed/34571922
http://dx.doi.org/10.3390/cells10092276
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author Istiaq, Arif
Ohta, Kunimasa
author_facet Istiaq, Arif
Ohta, Kunimasa
author_sort Istiaq, Arif
collection PubMed
description The ribosome, which is present in all three domains of life, plays a well-established, critical role in the translation process by decoding messenger RNA into protein. Ribosomal proteins, in contrast, appear to play non-translational roles in growth, differentiation, and disease. We recently discovered that ribosomes are involved in reverting cellular potency to a multipotent state. Ribosomal incorporation (the uptake of free ribosome by living cells) can direct the fate of both somatic and cancer cells into multipotency, allowing them to switch cell lineage. During this process, both types of cells experienced cell-cycle arrest and cellular stress while remaining multipotent. This review provides a molecular perspective on current insights into ribosome-induced multipotency and sheds light on how a common stress-associated mechanism may be involved. We also discuss the impact of this phenomenon on cancer cell reprogramming and its potential in cancer therapy.
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spelling pubmed-84692042021-09-27 Ribosome-Induced Cellular Multipotency, an Emerging Avenue in Cell Fate Reversal Istiaq, Arif Ohta, Kunimasa Cells Review The ribosome, which is present in all three domains of life, plays a well-established, critical role in the translation process by decoding messenger RNA into protein. Ribosomal proteins, in contrast, appear to play non-translational roles in growth, differentiation, and disease. We recently discovered that ribosomes are involved in reverting cellular potency to a multipotent state. Ribosomal incorporation (the uptake of free ribosome by living cells) can direct the fate of both somatic and cancer cells into multipotency, allowing them to switch cell lineage. During this process, both types of cells experienced cell-cycle arrest and cellular stress while remaining multipotent. This review provides a molecular perspective on current insights into ribosome-induced multipotency and sheds light on how a common stress-associated mechanism may be involved. We also discuss the impact of this phenomenon on cancer cell reprogramming and its potential in cancer therapy. MDPI 2021-09-01 /pmc/articles/PMC8469204/ /pubmed/34571922 http://dx.doi.org/10.3390/cells10092276 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Istiaq, Arif
Ohta, Kunimasa
Ribosome-Induced Cellular Multipotency, an Emerging Avenue in Cell Fate Reversal
title Ribosome-Induced Cellular Multipotency, an Emerging Avenue in Cell Fate Reversal
title_full Ribosome-Induced Cellular Multipotency, an Emerging Avenue in Cell Fate Reversal
title_fullStr Ribosome-Induced Cellular Multipotency, an Emerging Avenue in Cell Fate Reversal
title_full_unstemmed Ribosome-Induced Cellular Multipotency, an Emerging Avenue in Cell Fate Reversal
title_short Ribosome-Induced Cellular Multipotency, an Emerging Avenue in Cell Fate Reversal
title_sort ribosome-induced cellular multipotency, an emerging avenue in cell fate reversal
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469204/
https://www.ncbi.nlm.nih.gov/pubmed/34571922
http://dx.doi.org/10.3390/cells10092276
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