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

Authors :
O'Brien CM
Chy HS
Zhou Q
Blumenfeld S
Lambshead JW
Liu X
Kie J
Capaldo BD
Chung TL
Adams TE
Phan T
Bentley JD
McKinstry WJ
Oliva K
McMurrick PJ
Wang YC
Rossello FJ
Lindeman GJ
Chen D
Jarde T
Clark AT
Abud HE
Visvader JE
Nefzger CM
Polo JM
Loring JF
Laslett AL
Source :
Stem cells (Dayton, Ohio) [Stem Cells] 2017 Mar; Vol. 35 (3), pp. 626-640. Date of Electronic Publication: 2017 Jan 19.
Publication Year :
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. Stem Cells 2017;35:626-640.<br /> (© 2016 The Authors Stem Cells published by Wiley Periodicals, Inc. on behalf of AlphaMed Press.)

Details

Language :
English
ISSN :
1549-4918
Volume :
35
Issue :
3
Database :
MEDLINE
Journal :
Stem cells (Dayton, Ohio)
Publication Type :
Academic Journal
Accession number :
28009074
Full Text :
https://doi.org/10.1002/stem.2558