Kang Lei, Yao Chunping, Khodadadi-Jamayran Alireza, Xu Weihua, Zhang Ruowen, Banerjee Nilam Sanjib, Chang Chia-Wei, Chow Louise T, Townes Tim, Hu Kejin
1 Stem Cell Institute, Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham , Birmingham, Alabama.
2 Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham , Birmingham, Alabama.
Stem Cells Dev. 2016 Apr 1;25(7):556-68. doi: 10.1089/scd.2015.0321.
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.
足突细胞黏蛋白样蛋白(PODXL)是CD34家族蛋白的成员。它是一种携带许多翻译后表位的蛋白质,这些表位负责多种多能性表面标志物,包括TRA-1-60、TRA-1-81、GCTM2、GP200和单克隆抗体84。然而,PODXL尚未引起干细胞生物学家的关注。在此,我们报告了多能干细胞中PODXL mRNA和蛋白质的几个特征。与依赖修饰的多能性表位类似,PODXL转录本和载体蛋白也是多能性的特征。PODXL在从卵母细胞到四细胞阶段的早期人类胚胎中高度表达。在人类细胞重编程为多能性的过程中,与TRA-1-60和TRA-1-81不同,PODXL在重编程的非常早期就被KLF4激活。尽管TRA-1-60和TRA-1-81在分化后完全消失,但即使在长期分化后仍存在残余的PODXL(+)群体,并且它们通过通用的人类PODXL表位3D3得以鉴定。与灵长类多能干细胞(PSC)特有的TRA-1-60和TRA-1-81表位不同,PODXL载体蛋白可以用作小鼠表面标志物。最重要的是,针对3D3表位的抗体可导致人类PSC(hPSC)大量坏死和凋亡。我们建议可以使用3D3抗体来消除hPSC衍生细胞中用于细胞移植的致瘤性多能细胞。