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The novel tool of cell reprogramming for applications in molecular medicine

Recent discoveries in the field of stem cell biology have enabled scientists to “reprogram” cells from one type to another. For example, it is now possible to place adult skin or blood cells in a dish and convert them into neurons, liver, or heart cells. It is also possible to literally “rejuvenate”...

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Autores principales: Mall, Moritz, Wernig, Marius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487694/
https://www.ncbi.nlm.nih.gov/pubmed/28597071
http://dx.doi.org/10.1007/s00109-017-1550-4
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author Mall, Moritz
Wernig, Marius
author_facet Mall, Moritz
Wernig, Marius
author_sort Mall, Moritz
collection PubMed
description Recent discoveries in the field of stem cell biology have enabled scientists to “reprogram” cells from one type to another. For example, it is now possible to place adult skin or blood cells in a dish and convert them into neurons, liver, or heart cells. It is also possible to literally “rejuvenate” adult cells by reprogramming them into embryonic-like stem cells, which in turn can be differentiated into every tissue and cell type of the human body. Our ability to reprogram cell types has four main implications for medicine: (1) scientists can now take skin or blood cells from patients and convert them to other cells to study disease processes. This disease modeling approach has the advantage over animal models because it is directly based on human patient cells. (2) Reprogramming could also be used as a “clinical trial in a dish” to evaluate the general efficacy and safety of newly developed drugs on human patient cells before they would be tested in animal models or people. (3) In addition, many drugs have deleterious side effects like heart arrhythmias in only a small and unpredictable subpopulation of patients. Reprogramming could facilitate precision medicine by testing the safety of already approved drugs first on reprogrammed patient cells in a personalized manner prior to administration. For example, drugs known to sometimes cause arrhythmias could be first tested on reprogrammed heart cells from individual patients. (4) Finally, reprogramming allows the generation of new tissues that could be grafted therapeutically to regenerate lost or damaged cells.
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spelling pubmed-54876942017-07-03 The novel tool of cell reprogramming for applications in molecular medicine Mall, Moritz Wernig, Marius J Mol Med (Berl) Review Recent discoveries in the field of stem cell biology have enabled scientists to “reprogram” cells from one type to another. For example, it is now possible to place adult skin or blood cells in a dish and convert them into neurons, liver, or heart cells. It is also possible to literally “rejuvenate” adult cells by reprogramming them into embryonic-like stem cells, which in turn can be differentiated into every tissue and cell type of the human body. Our ability to reprogram cell types has four main implications for medicine: (1) scientists can now take skin or blood cells from patients and convert them to other cells to study disease processes. This disease modeling approach has the advantage over animal models because it is directly based on human patient cells. (2) Reprogramming could also be used as a “clinical trial in a dish” to evaluate the general efficacy and safety of newly developed drugs on human patient cells before they would be tested in animal models or people. (3) In addition, many drugs have deleterious side effects like heart arrhythmias in only a small and unpredictable subpopulation of patients. Reprogramming could facilitate precision medicine by testing the safety of already approved drugs first on reprogrammed patient cells in a personalized manner prior to administration. For example, drugs known to sometimes cause arrhythmias could be first tested on reprogrammed heart cells from individual patients. (4) Finally, reprogramming allows the generation of new tissues that could be grafted therapeutically to regenerate lost or damaged cells. Springer Berlin Heidelberg 2017-06-08 2017 /pmc/articles/PMC5487694/ /pubmed/28597071 http://dx.doi.org/10.1007/s00109-017-1550-4 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Mall, Moritz
Wernig, Marius
The novel tool of cell reprogramming for applications in molecular medicine
title The novel tool of cell reprogramming for applications in molecular medicine
title_full The novel tool of cell reprogramming for applications in molecular medicine
title_fullStr The novel tool of cell reprogramming for applications in molecular medicine
title_full_unstemmed The novel tool of cell reprogramming for applications in molecular medicine
title_short The novel tool of cell reprogramming for applications in molecular medicine
title_sort novel tool of cell reprogramming for applications in molecular medicine
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487694/
https://www.ncbi.nlm.nih.gov/pubmed/28597071
http://dx.doi.org/10.1007/s00109-017-1550-4
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