Authors

Caroline B Pantazis
Andrian Yang
Erika Lara
Justin A McDonough, The Jackson LaboratoryFollow
Cornelis Blauwendraat
Lirong Peng
Hideyuki Oguro, The Jackson LaboratoryFollow
Jitendra Kanaujiya, The Jackson Laboratory
Jizhong Zou
David Sebesta
Gretchen Pratt
Erin Cross
Jeffrey Blockwick
Philip Buxton
Lauren Kinner-Bibeau
Constance Medura
Christopher Tompkins
Stephen Hughes
Marianita Santiana
Faraz Faghri
Mike A Nalls
Daniel Vitale
Shannon Ballard
Yue A Qi
Daniel M Ramos
Kailyn M Anderson
Julia Stadler
Priyanka Narayan
Jason Papademetriou
Luke Reilly
Matthew P Nelson
Sanya Aggarwal
Leah U Rosen
Peter Kirwan
Venkat Pisupati
Steven L Coon
Sonja W Scholz
Theresa Priebe
Miriam Öttl
Jian Dong
Marieke Meijer
Lara J M Janssen
Vanessa S Lourenco
Rik van der Kant
Dennis Crusius
Dominik Paquet
Ana-Caroline Raulin
Guojun Bu
Aaron Held
Brian J Wainger
Rebecca M C Gabriele
Jackie M Casey
Selina Wray
Dad Abu-Bonsrah
Clare L Parish
Melinda S Beccari
Don W Cleveland
Emmy Li
Indigo V L Rose
Martin Kampmann
Carles Calatayud Aristoy
Patrik Verstreken
Laurin Heinrich
Max Y Chen
Birgitt Schüle
Dan Dou
Erika L F Holzbaur
Maria Clara Zanellati
Richa Basundra
Mohanish Deshmukh
Sarah Cohen
Richa Khanna
Malavika Raman
Zachary S Nevin
Madeline Matia
Jonas Van Lent
Vincent Timmerman
Bruce R Conklin
Katherine Johnson Chase
Ke Zhang
Salome Funes
Daryl A Bosco
Lena Erlebach
Marc Welzer
Deborah Kronenberg-Versteeg
Guochang Lyu
Ernest Arenas
Elena Coccia
Lily Sarrafha
Tim Ahfeldt
John C Marioni
William C Skarnes, The Jackson LaboratoryFollow
Mark R Cookson
Michael E Ward
Florian T Merkle

Document Type

Article

Publication Date

12-1-2022

Publication Title

Cell Stem Cell

Keywords

JGM, SS1, Humans, Induced Pluripotent Stem Cells, Cell Differentiation, Gene Editing, Biological Assay

JAX Source

Cell Stem Cell. 2022;29(12):1685-702.e22.

Volume

29

Issue

12

First Page

1685

Last Page

1702

ISSN

1875-9777

PMID

36459969

DOI

https://doi.org/10.1016/j.stem.2022.11.004

Abstract

Human induced pluripotent stem cell (iPSC) lines are a powerful tool for studying development and disease, but the considerable phenotypic variation between lines makes it challenging to replicate key findings and integrate data across research groups. To address this issue, we sub-cloned candidate human iPSC lines and deeply characterized their genetic properties using whole genome sequencing, their genomic stability upon CRISPR-Cas9-based gene editing, and their phenotypic properties including differentiation to commonly used cell types. These studies identified KOLF2.1J as an all-around well-performing iPSC line. We then shared KOLF2.1J with groups around the world who tested its performance in head-to-head comparisons with their own preferred iPSC lines across a diverse range of differentiation protocols and functional assays. On the strength of these findings, we have made KOLF2.1J and its gene-edited derivative clones readily accessible to promote the standardization required for large-scale collaborative science in the stem cell field.

Comments

This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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