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Embryonic stem cells: An alternative approach to developmental toxicity testing

Stem cells in the body have a unique ability to renew themselves and give rise to more specialized cell types having functional commitments. Under specified growth conditions, these cell types remain unspecialized but can be triggered to become specific cell type of the body such as heart, nerve, or...

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Detalles Bibliográficos
Autores principales: Tandon, S., Jyoti, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341726/
https://www.ncbi.nlm.nih.gov/pubmed/22557918
http://dx.doi.org/10.4103/0975-7406.94808
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author Tandon, S.
Jyoti, S.
author_facet Tandon, S.
Jyoti, S.
author_sort Tandon, S.
collection PubMed
description Stem cells in the body have a unique ability to renew themselves and give rise to more specialized cell types having functional commitments. Under specified growth conditions, these cell types remain unspecialized but can be triggered to become specific cell type of the body such as heart, nerve, or skin cells. This ability of embryonic stem cells for directed differentiation makes it a prominent candidate as a screening tool in revealing safer and better drugs. In addition, genetic variations and birth defects caused by mutations and teratogens affecting early human development could also be studied on this basis. Moreover, replacement of animal testing is needed because it involves ethical, legal, and cost issues. Thus, there is a strong requirement for validated and reliable, if achievable, human stem cell-based developmental assays for pharmacological and toxicological screening.
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spelling pubmed-33417262012-05-03 Embryonic stem cells: An alternative approach to developmental toxicity testing Tandon, S. Jyoti, S. J Pharm Bioallied Sci Review Article Stem cells in the body have a unique ability to renew themselves and give rise to more specialized cell types having functional commitments. Under specified growth conditions, these cell types remain unspecialized but can be triggered to become specific cell type of the body such as heart, nerve, or skin cells. This ability of embryonic stem cells for directed differentiation makes it a prominent candidate as a screening tool in revealing safer and better drugs. In addition, genetic variations and birth defects caused by mutations and teratogens affecting early human development could also be studied on this basis. Moreover, replacement of animal testing is needed because it involves ethical, legal, and cost issues. Thus, there is a strong requirement for validated and reliable, if achievable, human stem cell-based developmental assays for pharmacological and toxicological screening. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3341726/ /pubmed/22557918 http://dx.doi.org/10.4103/0975-7406.94808 Text en Copyright: © Journal of Pharmacy and Bioallied Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Tandon, S.
Jyoti, S.
Embryonic stem cells: An alternative approach to developmental toxicity testing
title Embryonic stem cells: An alternative approach to developmental toxicity testing
title_full Embryonic stem cells: An alternative approach to developmental toxicity testing
title_fullStr Embryonic stem cells: An alternative approach to developmental toxicity testing
title_full_unstemmed Embryonic stem cells: An alternative approach to developmental toxicity testing
title_short Embryonic stem cells: An alternative approach to developmental toxicity testing
title_sort embryonic stem cells: an alternative approach to developmental toxicity testing
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341726/
https://www.ncbi.nlm.nih.gov/pubmed/22557918
http://dx.doi.org/10.4103/0975-7406.94808
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