Cargando…
Multiple sclerosis: getting personal with induced pluripotent stem cells
Human induced pluripotent stem (iPS) cells can be derived from lineage-restricted cells and represent an important tool to develop novel patient-specific cell therapies and research models for inherited and acquired diseases. Recently, patient-derived iPS cells, containing donor genetic background,...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650727/ https://www.ncbi.nlm.nih.gov/pubmed/26158512 http://dx.doi.org/10.1038/cddis.2015.179 |
_version_ | 1782401546553655296 |
---|---|
author | Di Ruscio, A Patti, F Welner, R S Tenen, D G Amabile, G |
author_facet | Di Ruscio, A Patti, F Welner, R S Tenen, D G Amabile, G |
author_sort | Di Ruscio, A |
collection | PubMed |
description | Human induced pluripotent stem (iPS) cells can be derived from lineage-restricted cells and represent an important tool to develop novel patient-specific cell therapies and research models for inherited and acquired diseases. Recently, patient-derived iPS cells, containing donor genetic background, have offered a breakthrough approach to study human genetics of neurodegenerative diseases. By offering an unlimited source of patient-specific disease-relevant cells, iPS cells hold great promise for understanding disease mechanisms, identifying molecular targets and developing phenotypic screens for drug discovery. This review will discuss the potential impact of using iPS cell-derived models in multiple sclerosis (MS) research and highlight some of the current challenges and prospective for generating novel therapeutic treatments for MS patients. |
format | Online Article Text |
id | pubmed-4650727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46507272015-12-02 Multiple sclerosis: getting personal with induced pluripotent stem cells Di Ruscio, A Patti, F Welner, R S Tenen, D G Amabile, G Cell Death Dis Review Human induced pluripotent stem (iPS) cells can be derived from lineage-restricted cells and represent an important tool to develop novel patient-specific cell therapies and research models for inherited and acquired diseases. Recently, patient-derived iPS cells, containing donor genetic background, have offered a breakthrough approach to study human genetics of neurodegenerative diseases. By offering an unlimited source of patient-specific disease-relevant cells, iPS cells hold great promise for understanding disease mechanisms, identifying molecular targets and developing phenotypic screens for drug discovery. This review will discuss the potential impact of using iPS cell-derived models in multiple sclerosis (MS) research and highlight some of the current challenges and prospective for generating novel therapeutic treatments for MS patients. Nature Publishing Group 2015-07 2015-07-09 /pmc/articles/PMC4650727/ /pubmed/26158512 http://dx.doi.org/10.1038/cddis.2015.179 Text en Copyright © 2015 Macmillan Publishers Limited |
spellingShingle | Review Di Ruscio, A Patti, F Welner, R S Tenen, D G Amabile, G Multiple sclerosis: getting personal with induced pluripotent stem cells |
title | Multiple sclerosis: getting personal with induced pluripotent stem cells |
title_full | Multiple sclerosis: getting personal with induced pluripotent stem cells |
title_fullStr | Multiple sclerosis: getting personal with induced pluripotent stem cells |
title_full_unstemmed | Multiple sclerosis: getting personal with induced pluripotent stem cells |
title_short | Multiple sclerosis: getting personal with induced pluripotent stem cells |
title_sort | multiple sclerosis: getting personal with induced pluripotent stem cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650727/ https://www.ncbi.nlm.nih.gov/pubmed/26158512 http://dx.doi.org/10.1038/cddis.2015.179 |
work_keys_str_mv | AT diruscioa multiplesclerosisgettingpersonalwithinducedpluripotentstemcells AT pattif multiplesclerosisgettingpersonalwithinducedpluripotentstemcells AT welnerrs multiplesclerosisgettingpersonalwithinducedpluripotentstemcells AT tenendg multiplesclerosisgettingpersonalwithinducedpluripotentstemcells AT amabileg multiplesclerosisgettingpersonalwithinducedpluripotentstemcells |