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The Universal 3D3 Antibody of Human PODXL Is Pluripotent Cytotoxic, and Identifies a Residual Population After Extended Differentiation of Pluripotent Stem Cells.

Authors :
Kang, Lei
Yao, Chunping
Khodadadi-Jamayran, Alireza
Xu, Weihua
Zhang, Ruowen
Banerjee, Nilam Sanjib
Chang, Chia-Wei
Chow, Louise T.
Townes, Tim
Hu, Kejin
Source :
Stem Cells & Development. Apr2016, Vol. 25 Issue 7, p556-568. 13p.
Publication Year :
2016

Abstract

Podocalyxin-like protein (PODXL) is a member of CD34 family proteins. It is the protein that carries many post-translational epitopes responsible for various pluripotent surface markers including TRA-1-60, TRA-1-81, GCTM2, GP200, and mAb84. However, PODXL has not attracted the attention of stem cell biologists. Here, we report several features of PODXL mRNA and protein in pluripotent stem cells. Similar to the modification-dependent pluripotent epitopes, PODXL transcripts and carrier protein are also features of pluripotency. PODXL is highly expressed in early human embryos from oocytes up to four-cell stages. During reprogramming of human cells to pluripotency, in contrast to TRA-1-60 and TRA-1-81, PODXL is activated by KLF4 at a very early time of reprogramming. Although TRA-1-60 and TRA-1-81 are completely lost upon differentiation, a residual PODXL+ population exists even after extended differentiation and they were identified by the universal human PODXL epitope 3D3. Unlike TRA-1-60 and TRA-1-81 epitopes that are unique to primate pluripotent stem cells (PSCs), PODXL carrier protein can be used as a murine surface marker. Most importantly, antibody to 3D3 epitope causes massive necrosis and apoptosis of human PSCs (hPSCs). We suggest that 3D3 antibody could be employed to eliminate the tumorigenic pluripotent cells in hPSC-derived cells for cell transplantation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15473287
Volume :
25
Issue :
7
Database :
Academic Search Index
Journal :
Stem Cells & Development
Publication Type :
Academic Journal
Accession number :
114077655
Full Text :
https://doi.org/10.1089/scd.2015.0321