Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndrome.

TitleRecapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndrome.
Publication TypeJournal Article
Year of Publication2011
AuthorsLiu G-H, Barkho BZ, Ruiz S, Diep D, Qu J, Yang S-L, Panopoulos AD, Suzuki K, Kurian L, Walsh C, Thompson J, Boue S, Fung H L, Sancho-Martinez I, Zhang K, Yates J, Izpisua Belmonte J C
JournalNature
Volume472
Issue7342
Pagination221-5
Date Published2011 Apr 14
ISSN1476-4687
KeywordsAging, Aging, Premature, Calcium-Binding Proteins, Cell Aging, Cell Differentiation, Cell Line, DNA-Activated Protein Kinase, Epigenesis, Genetic, Fibroblasts, Holoenzymes, Humans, Induced Pluripotent Stem Cells, Microfilament Proteins, Models, Biological, Muscle, Smooth, Vascular, Nuclear Envelope, Nuclear Proteins, Nuclear Reprogramming, Phenotype, Progeria, Protein Precursors, Substrate Specificity
Abstract

Hutchinson-Gilford progeria syndrome (HGPS) is a rare and fatal human premature ageing disease, characterized by premature arteriosclerosis and degeneration of vascular smooth muscle cells (SMCs). HGPS is caused by a single point mutation in the lamin A (LMNA) gene, resulting in the generation of progerin, a truncated splicing mutant of lamin A. Accumulation of progerin leads to various ageing-associated nuclear defects including disorganization of nuclear lamina and loss of heterochromatin. Here we report the generation of induced pluripotent stem cells (iPSCs) from fibroblasts obtained from patients with HGPS. HGPS-iPSCs show absence of progerin, and more importantly, lack the nuclear envelope and epigenetic alterations normally associated with premature ageing. Upon differentiation of HGPS-iPSCs, progerin and its ageing-associated phenotypic consequences are restored. Specifically, directed differentiation of HGPS-iPSCs to SMCs leads to the appearance of premature senescence phenotypes associated with vascular ageing. Additionally, our studies identify DNA-dependent protein kinase catalytic subunit (DNAPKcs, also known as PRKDC) as a downstream target of progerin. The absence of nuclear DNAPK holoenzyme correlates with premature as well as physiological ageing. Because progerin also accumulates during physiological ageing, our results provide an in vitro iPSC-based model to study the pathogenesis of human premature and physiological vascular ageing.

DOI10.1038/nature09879
PubMed URLhttp://www.ncbi.nlm.nih.gov/pubmed/21346760?dopt=Abstract
PMCPMC3088088
Alternate TitleNature
PubMed ID21346760