Generating late-onset human iPSC-based disease models by inducing neuronal age-related phenotypes through telomerase manipulation Journal Article


Authors: Vera, E.; Bosco, N.; Studer, L.
Article Title: Generating late-onset human iPSC-based disease models by inducing neuronal age-related phenotypes through telomerase manipulation
Abstract: Modeling late-onset disorders such as Parkinson's disease (PD) using iPSC technology remains a challenge, as current differentiation protocols yield cells with the properties of fetal-stage cells. Here, we tested whether it is possible to accelerate aging in vitro to trigger late-onset disease phenotypes in an iPSC model of PD. In order to manipulate a factor that is involved in natural aging as well as in premature aging syndromes, we used telomere shortening as an age-inducing tool. We show that shortened telomeres result in age-associated as well as potentially disease-associated phenotypes in human pluripotent stem cell (hPSC)-derived midbrain dopamine (mDA) neurons. Our approach provides proof of concept for the further validation of telomere shortening as an induced-aging tool for late-onset-disease modeling. © 2016 The Authors
Keywords: telomerase; aging; disease modeling; ipsc; telomeres; induced aging; late-onset disease; neuronal aging
Journal Title: Cell Reports
Volume: 17
Issue: 4
ISSN: 2211-1247
Publisher: Cell Press  
Date Published: 2016-10-18
Start Page: 1184
End Page: 1192
Language: English
DOI: 10.1016/j.celrep.2016.09.062
PROVIDER: scopus
PMCID: PMC5089807
PUBMED: 27760320
DOI/URL:
Notes: Article -- Export Date: 6 December 2016 -- Source: Scopus
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  1. Lorenz Studer
    220 Studer
  2. Elsa Vera
    5 Vera