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Cell Immortalization: In Vivo Molecular Bases and In Vitro Techniques for Obtention

Somatic human cells can divide a finite number of times, a phenomenon known as the Hayflick limit. It is based on the progressive erosion of the telomeric ends each time the cell completes a replicative cycle. Given this problem, researchers need cell lines that do not enter the senescence phase aft...

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Autores principales: de Bardet, Javier Curi, Cardentey, Celeste Ramírez, González, Belkis López, Patrone, Deanira, Mulet, Idania Lores, Siniscalco, Dario, Robinson-Agramonte, María de los Angeles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944833/
https://www.ncbi.nlm.nih.gov/pubmed/36810441
http://dx.doi.org/10.3390/biotech12010014
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author de Bardet, Javier Curi
Cardentey, Celeste Ramírez
González, Belkis López
Patrone, Deanira
Mulet, Idania Lores
Siniscalco, Dario
Robinson-Agramonte, María de los Angeles
author_facet de Bardet, Javier Curi
Cardentey, Celeste Ramírez
González, Belkis López
Patrone, Deanira
Mulet, Idania Lores
Siniscalco, Dario
Robinson-Agramonte, María de los Angeles
author_sort de Bardet, Javier Curi
collection PubMed
description Somatic human cells can divide a finite number of times, a phenomenon known as the Hayflick limit. It is based on the progressive erosion of the telomeric ends each time the cell completes a replicative cycle. Given this problem, researchers need cell lines that do not enter the senescence phase after a certain number of divisions. In this way, more lasting studies can be carried out over time and avoid the tedious work involved in performing cell passes to fresh media. However, some cells have a high replicative potential, such as embryonic stem cells and cancer cells. To accomplish this, these cells express the enzyme telomerase or activate the mechanisms of alternative telomere elongation, which favors the maintenance of the length of their stable telomeres. Researchers have been able to develop cell immortalization technology by studying the cellular and molecular bases of both mechanisms and the genes involved in the control of the cell cycle. Through it, cells with infinite replicative capacity are obtained. To obtain them, viral oncogenes/oncoproteins, myc genes, ectopic expression of telomerase, and the manipulation of genes that regulate the cell cycle, such as p53 and Rb, have been used.
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spelling pubmed-99448332023-02-23 Cell Immortalization: In Vivo Molecular Bases and In Vitro Techniques for Obtention de Bardet, Javier Curi Cardentey, Celeste Ramírez González, Belkis López Patrone, Deanira Mulet, Idania Lores Siniscalco, Dario Robinson-Agramonte, María de los Angeles BioTech (Basel) Review Somatic human cells can divide a finite number of times, a phenomenon known as the Hayflick limit. It is based on the progressive erosion of the telomeric ends each time the cell completes a replicative cycle. Given this problem, researchers need cell lines that do not enter the senescence phase after a certain number of divisions. In this way, more lasting studies can be carried out over time and avoid the tedious work involved in performing cell passes to fresh media. However, some cells have a high replicative potential, such as embryonic stem cells and cancer cells. To accomplish this, these cells express the enzyme telomerase or activate the mechanisms of alternative telomere elongation, which favors the maintenance of the length of their stable telomeres. Researchers have been able to develop cell immortalization technology by studying the cellular and molecular bases of both mechanisms and the genes involved in the control of the cell cycle. Through it, cells with infinite replicative capacity are obtained. To obtain them, viral oncogenes/oncoproteins, myc genes, ectopic expression of telomerase, and the manipulation of genes that regulate the cell cycle, such as p53 and Rb, have been used. MDPI 2023-01-28 /pmc/articles/PMC9944833/ /pubmed/36810441 http://dx.doi.org/10.3390/biotech12010014 Text en © 2023 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
de Bardet, Javier Curi
Cardentey, Celeste Ramírez
González, Belkis López
Patrone, Deanira
Mulet, Idania Lores
Siniscalco, Dario
Robinson-Agramonte, María de los Angeles
Cell Immortalization: In Vivo Molecular Bases and In Vitro Techniques for Obtention
title Cell Immortalization: In Vivo Molecular Bases and In Vitro Techniques for Obtention
title_full Cell Immortalization: In Vivo Molecular Bases and In Vitro Techniques for Obtention
title_fullStr Cell Immortalization: In Vivo Molecular Bases and In Vitro Techniques for Obtention
title_full_unstemmed Cell Immortalization: In Vivo Molecular Bases and In Vitro Techniques for Obtention
title_short Cell Immortalization: In Vivo Molecular Bases and In Vitro Techniques for Obtention
title_sort cell immortalization: in vivo molecular bases and in vitro techniques for obtention
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944833/
https://www.ncbi.nlm.nih.gov/pubmed/36810441
http://dx.doi.org/10.3390/biotech12010014
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