New Monoclonal Antibodies to Defined Cell Surface Proteins on Human Pluripotent Stem Cells. (19th January 2017)

• Record Type: Journal Article
• Authors: O'Brien, Carmel M.; Chy, Hun S.; Zhou, Qi; Blumenfeld, Shiri; Lambshead, Jack W.; Liu, Xiaodong; Kie, Joshua; Capaldo, Bianca D.; Chung, Tung-Liang; Adams, Timothy E.; Phan, Tram; Bentley, John D.; McKinstry, William J.; Oliva, Karen; McMurrick, Paul J.; Wang, Yu-Chieh; Rossello, Fernando J.; Lindeman, Geoffrey J.; Chen, Di; Jarde, Thierry; Clark, Amander T.; Abud, Helen E.; Visvader, Jane E.; Nefzger, Christian M.; Polo, Jose M.; Loring, Jeanne F.; Laslett, Andrew L.
• Is Part Of: Stem cells. Volume 35:Number 3(2017:Mar.)
• Page Start: 626
• Page End: 640
• Publication Date: 2017-01-19
• Subjects: Pluripotency -- Human embryonic stem cells -- Human iPS cells -- Naive -- Breast -- Colorectal -- Cell surface markers -- Monoclonal antibodies -- Cancer; Cloning -- Periodicals; Clone cells -- Periodicals; Stem cells -- Periodicals; Cell Differentiation -- Periodicals; Cell Division -- Periodicals; Clone Cells -- Periodicals; Hematopoietic Stem Cells -- Periodicals; Stem Cells -- Periodicals; 571.84
• DOI: 10.1002/stem.2558
• Languages: English
• ISSNs: 1066-5099

Abstract

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.