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

Author:

O'Brien Carmel M.12,Chy Hun S.12,Zhou Qi12,Blumenfeld Shiri1,Lambshead Jack W.12,Liu Xiaodong23,Kie Joshua13,Capaldo Bianca D.45,Chung Tung-Liang12,Adams Timothy E.1,Phan Tram1,Bentley John D.1,McKinstry William J.1,Oliva Karen6,McMurrick Paul J.6,Wang Yu-Chieh78,Rossello Fernando J.23,Lindeman Geoffrey J.4910,Chen Di11,Jarde Thierry31213,Clark Amander T.11,Abud Helen E.312,Visvader Jane E.45,Nefzger Christian M.23,Polo Jose M.23,Loring Jeanne F.78,Laslett Andrew L.12

Affiliation:

1. a Clayton and Parkville, CSIRO Manufacturing, Victoria, Australia

2. b Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia

3. c Department of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia

4. d The Walter and Eliza Hall Institute (WEHI), Parkville, Victoria, Australia

5. e Department of Medical Biology

6. f Department of Surgery, Cabrini Monash University, Malvern, Victoria, Australia

7. g Department of Chemical Physiology

8. h Center for Regenerative Medicine, The Scripps Research Institute, La Jolla, California, USA

9. i Department of Medicine, The University of Melbourne, Parkville, Victoria, Australia

10. j Department of Medical Oncology, The Royal Melbourne Hospital, Parkville, Victoria, Australia

11. k Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, California, USA

12. l Cancer Program, Monash Biomedicine Discovery Institute

13. m Centre for Cancer Research, Hudson Institute of Medical Research, Clayton, Victoria, Australia

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.

Funder

California Institute for Regenerative Medicine

State Government of Victoria

Australia's National Health and Medical Research Council

Australian Research Council

Anastasia Lukianchikov

WEHI Flow Cytometry

Victorian Cancer Biobank and Cabrini Hospitals

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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