| Literature DB >> 26395137 |
Abstract
In contrast to the successful modeling of early-onset disorders using patient-specific cells, modeling of late-onset neurodegenerative diseases such as Parkinson's disease remains a challenge. This might be related to the often ignored fact that current induced pluripotent stem cell (iPSC) differentiation protocols yield cells that typically show the behavior of fetal stage cells. Acknowledging aging as a contributing factor in late-onset neurodegenerative disorders represents an important step on the road towards faithfully recreating these diseases in vitro. Here, we summarize progress in the field and review the strategies and challenges for triggering late-onset disease phenotypes.Entities:
Keywords: Aging; Disease modeling; Rejuvenation
Mesh:
Year: 2015 PMID: 26395137 PMCID: PMC6514401 DOI: 10.1242/dev.120667
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868