Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/133641
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Type: Journal article
Title: New monoclonal antibodies to defined cell surface proteins on human pluripotent stem cells
Author: O’Brien, C.M.
Chy, H.S.
Zhou, Q.
Blumenfeld, S.
Lambshead, J.W.
Liu, X.
Kie, J.
Capaldo, B.D.
Chung, T.L.
Adams, T.E.
Phan, T.
Bentley, J.D.
McKinstry, W.J.
Oliva, K.
McMurrick, P.J.
Wang, Y.C.
Rossello, F.J.
Lindeman, G.J.
Chen, D.
Jarde, T.
et al.
Citation: Stem Cells, 2017; 35(3):626-640
Publisher: Wiley
Issue Date: 2017
ISSN: 1066-5099
1549-4918
Statement of
Responsibility: 
Carmel M. O'Brien, Hun S. Chy, Qi Zhou, Shiri Blumenfeld, Jack W. Lambshead, Xiaodong Liu ... et al.
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.
Keywords: Hematopoietic Stem Cells
Pluripotent Stem Cells
Animals
Humans
Mice
Membrane Proteins
Antibodies, Monoclonal
Antigens, Surface
Flow Cytometry
Cell Culture Techniques
Cell Differentiation
Down-Regulation
Octamer Transcription Factor-3
Embryoid Bodies
Cell Self Renewal
Rights: © 2016 The Authors STEM CELLS published by Wiley Periodicals, Inc. on behalf of AlphaMed Press. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited
DOI: 10.1002/stem.2558
Published version: http://dx.doi.org/10.1002/stem.2558
Appears in Collections:Medicine publications

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