The University of Southampton
University of Southampton Institutional Repository

Transient naive reprogramming corrects hiPS cells functionally and epigenetically

Transient naive reprogramming corrects hiPS cells functionally and epigenetically
Transient naive reprogramming corrects hiPS cells functionally and epigenetically
Cells undergo a major epigenome reconfiguration when reprogrammed to human induced pluripotent stem cells (hiPS cells). However, the epigenomes of hiPS cells and human embryonic stem (hES) cells differ significantly, which affects hiPS cell function1,2,3,4,5,6,7,8. These differences include epigenetic memory and aberrations that emerge during reprogramming, for which the mechanisms remain unknown. Here we characterized the persistence and emergence of these epigenetic differences by performing genome-wide DNA methylation profiling throughout primed and naive reprogramming of human somatic cells to hiPS cells. We found that reprogramming-induced epigenetic aberrations emerge midway through primed reprogramming, whereas DNA demethylation begins early in naive reprogramming. Using this knowledge, we developed a transient-naive-treatment (TNT) reprogramming strategy that emulates the embryonic epigenetic reset. We show that the epigenetic memory in hiPS cells is concentrated in cell of origin-dependent repressive chromatin marked by H3K9me3, lamin-B1 and aberrant CpH methylation. TNT reprogramming reconfigures these domains to a hES cell-like state and does not disrupt genomic imprinting. Using an isogenic system, we demonstrate that TNT reprogramming can correct the transposable element overexpression and differential gene expression seen in conventional hiPS cells, and that TNT-reprogrammed hiPS and hES cells show similar differentiation efficiencies. Moreover, TNT reprogramming enhances the differentiation of hiPS cells derived from multiple cell types. Thus, TNT reprogramming corrects epigenetic memory and aberrations, producing hiPS cells that are molecularly and functionally more similar to hES cells than conventional hiPS cells. We foresee TNT reprogramming becoming a new standard for biomedical and therapeutic applications and providing a novel system for studying epigenetic memory.
0028-0836
863-872
Buckberry, Sam
fe0c626c-699f-4858-9572-5b1af9b18814
Liu, Xiaodong
e30fba98-1b4e-4b63-bd7e-708b96e28d44
Poppe, Daniel
84e4ffe5-8508-409a-9b2b-4c82e9127693
Rackham, Owen J.L.
8122eb1f-6e9f-4da5-90e1-ce108ccbbcbf
et al.
Buckberry, Sam
fe0c626c-699f-4858-9572-5b1af9b18814
Liu, Xiaodong
e30fba98-1b4e-4b63-bd7e-708b96e28d44
Poppe, Daniel
84e4ffe5-8508-409a-9b2b-4c82e9127693
Rackham, Owen J.L.
8122eb1f-6e9f-4da5-90e1-ce108ccbbcbf

et al. (2023) Transient naive reprogramming corrects hiPS cells functionally and epigenetically. Nature, 620, 863-872. (doi:10.1038/s41586-023-06424-7).

Record type: Article

Abstract

Cells undergo a major epigenome reconfiguration when reprogrammed to human induced pluripotent stem cells (hiPS cells). However, the epigenomes of hiPS cells and human embryonic stem (hES) cells differ significantly, which affects hiPS cell function1,2,3,4,5,6,7,8. These differences include epigenetic memory and aberrations that emerge during reprogramming, for which the mechanisms remain unknown. Here we characterized the persistence and emergence of these epigenetic differences by performing genome-wide DNA methylation profiling throughout primed and naive reprogramming of human somatic cells to hiPS cells. We found that reprogramming-induced epigenetic aberrations emerge midway through primed reprogramming, whereas DNA demethylation begins early in naive reprogramming. Using this knowledge, we developed a transient-naive-treatment (TNT) reprogramming strategy that emulates the embryonic epigenetic reset. We show that the epigenetic memory in hiPS cells is concentrated in cell of origin-dependent repressive chromatin marked by H3K9me3, lamin-B1 and aberrant CpH methylation. TNT reprogramming reconfigures these domains to a hES cell-like state and does not disrupt genomic imprinting. Using an isogenic system, we demonstrate that TNT reprogramming can correct the transposable element overexpression and differential gene expression seen in conventional hiPS cells, and that TNT-reprogrammed hiPS and hES cells show similar differentiation efficiencies. Moreover, TNT reprogramming enhances the differentiation of hiPS cells derived from multiple cell types. Thus, TNT reprogramming corrects epigenetic memory and aberrations, producing hiPS cells that are molecularly and functionally more similar to hES cells than conventional hiPS cells. We foresee TNT reprogramming becoming a new standard for biomedical and therapeutic applications and providing a novel system for studying epigenetic memory.

Text
s41586-023-06424-7 - Version of Record
Available under License Creative Commons Attribution.
Download (71MB)

More information

Accepted/In Press date: 11 July 2023
Published date: 16 August 2023

Identifiers

Local EPrints ID: 501096
URI: http://eprints.soton.ac.uk/id/eprint/501096
ISSN: 0028-0836
PURE UUID: 4e1569ca-3573-4797-93fe-1d9b06371fe5
ORCID for Owen J.L. Rackham: ORCID iD orcid.org/0000-0002-4390-0872

Catalogue record

Date deposited: 23 May 2025 16:48
Last modified: 22 Aug 2025 02:30

Export record

Altmetrics

Contributors

Author: Sam Buckberry
Author: Xiaodong Liu
Author: Daniel Poppe
Corporate Author: et al.

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×