Open AccessREST suppression mediates neural conversion of adult human fibroblasts via microRNA‐dependent and ‐independent pathways
Author(s) -
DrouinOuellet Janelle,
Lau Shong,
Brattås Per Ludvik,
Rylander Ottosson Daniella,
Pircs Karolina,
Grassi Daniela A,
Collins Lucy M,
Vuono Romina,
Andersson Sjöland Annika,
WestergrenThorsson Gunilla,
Graff Caroline,
Minthon Lennart,
Toresson Håkan,
Barker Roger A,
Jakobsson Johan,
Parmar Malin
Publication year - 2017
Publication title -
embo molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.923
H-Index - 107
eISSN - 1757-4684
pISSN - 1757-4676
DOI - 10.15252/emmm.201607471
Subject(s) - reprogramming , gene knockdown , rest (music) , rna , biology , small interfering rna , microrna , microbiology and biotechnology , gene , neuroscience , medicine , genetics
Direct conversion of human fibroblasts into mature and functional neurons, termed induced neurons ( iN s), was achieved for the first time 6 years ago. This technology offers a promising shortcut for obtaining patient‐ and disease‐specific neurons for disease modeling, drug screening, and other biomedical applications. However, fibroblasts from adult donors do not reprogram as easily as fetal donors, and no current reprogramming approach is sufficiently efficient to allow the use of this technology using patient‐derived material for large‐scale applications. Here, we investigate the difference in reprogramming requirements between fetal and adult human fibroblasts and identify REST as a major reprogramming barrier in adult fibroblasts. Via functional experiments where we overexpress and knockdown the REST ‐controlled neuron‐specific micro RNA s miR‐9 and miR‐124, we show that the effect of REST inhibition is only partially mediated via micro RNA up‐regulation. Transcriptional analysis confirmed that REST knockdown activates an overlapping subset of neuronal genes as micro RNA overexpression and also a distinct set of neuronal genes that are not activated via micro RNA overexpression. Based on this, we developed an optimized one‐step method to efficiently reprogram dermal fibroblasts from elderly individuals using a single‐vector system and demonstrate that it is possible to obtain iN s of high yield and purity from aged individuals with a range of familial and sporadic neurodegenerative disorders including Parkinson's, Huntington's, as well as Alzheimer's disease.