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New Monoclonal Antibodies to Defined Cell Surface Proteins on Human Pluripotent Stem Cells

Authors :
Bianca D. Capaldo
Helen E. Abud
Qi Zhou
Shiri Blumenfeld
Karen Oliva
Paul J. McMurrick
Joshua Kie
Geoffrey J. Lindeman
Jane E. Visvader
Andrew L. Laslett
William J. McKinstry
Timothy E. Adams
Di Chen
Christian M. Nefzger
Jose M. Polo
Thierry Jarde
John D. Bentley
Jeanne F. Loring
Jack W. Lambshead
Yu-Chieh Wang
Xiaodong Liu
Tung Liang Chung
Fernando J. Rossello
Carmel M. O’Brien
Tram Phan
Amander T. Clark
Hun S. Chy
Source :
Stem Cells (Dayton, Ohio), Stem cells (Dayton, Ohio), vol 35, iss 3
Publication Year :
2017
Publisher :
Oxford University Press (OUP), 2017.

Abstract

The study and application of human pluripotent stem cells (hPSCs) will be enhanced by the availability of well-characterized monoclonal antibodies (mAbs) detecting cell-surface epitopes. Here, we report generation of seven new mAbs that detect cell surface proteins present on live and fixed human ES cells (hESCs) and human iPS cells (hiPSCs), confirming our previous prediction that these proteins were present on the cell surface of hPSCs. The mAbs all show a high correlation with POU5F1 (OCT4) expression and other hPSC surface markers (TRA-160 and SSEA-4) in hPSC cultures and detect rare OCT4 positive cells in differentiated cell cultures. These mAbs are immunoreactive to cell surface protein epitopes on both primed and naive state hPSCs, providing useful research tools to investigate the cellular mechanisms underlying human pluripotency and states of cellular reprogramming. In addition, we report that subsets of the seven new mAbs are also immunoreactive to human bone marrow-derived mesenchymal stem cells (MSCs), normal human breast subsets and both normal and tumorigenic colorectal cell populations. The mAbs reported here should accelerate the investigation of the nature of pluripotency, and enable development of robust cell separation and tracing technologies to enrich or deplete for hPSCs and other human stem and somatic cell types.

Details

ISSN :
15494918 and 10665099
Volume :
35
Database :
OpenAIRE
Journal :
Stem Cells
Accession number :
edsair.doi.dedup.....04eabc3e899b2e23c30bdad68fe28fd5
Full Text :
https://doi.org/10.1002/stem.2558