Stem Cell Reports (Jul 2018)

DSG2 Is a Functional Cell Surface Marker for Identification and Isolation of Human Pluripotent Stem Cells

  • Jongjin Park,
  • Yeonsung Son,
  • Na Geum Lee,
  • Kyungmin Lee,
  • Dong Gwang Lee,
  • Jinhoi Song,
  • Jaemin Lee,
  • Seokho Kim,
  • Min Ji Cho,
  • Ju-Hong Jang,
  • Jangwook Lee,
  • Jong-Gil Park,
  • Yeon-Gu Kim,
  • Jang-Seong Kim,
  • Jungwoon Lee,
  • Yee Sook Cho,
  • Young-Jun Park,
  • Baek Soo Han,
  • Kwang-Hee Bae,
  • Seungmin Han,
  • Byunghoon Kang,
  • Seungjoo Haam,
  • Sang-Hyun Lee,
  • Sang Chul Lee,
  • Jeong-Ki Min

Journal volume & issue
Vol. 11, no. 1
pp. 115 – 127

Abstract

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Summary: Pluripotent stem cells (PSCs) represent the most promising clinical source for regenerative medicine. However, given the cellular heterogeneity within cultivation and safety concerns, the development of specific and efficient tools to isolate a pure population and eliminate all residual undifferentiated PSCs from differentiated derivatives is a prerequisite for clinical applications. In this study, we raised a monoclonal antibody and identified its target antigen as desmoglein-2 (DSG2). DSG2 co-localized with human PSC (hPSC)-specific cell surface markers, and its expression was rapidly downregulated upon differentiation. The depletion of DSG2 markedly decreased hPSC proliferation and pluripotency marker expression. In addition, DSG2-negative population in hPSCs exhibited a notable suppression in embryonic body and teratoma formation. The actions of DSG2 in regulating the self-renewal and pluripotency of hPSCs were predominantly exerted through the regulation of β-catenin/Slug-mediated epithelial-to-mesenchymal transition. Our results demonstrate that DSG2 is a valuable PSC surface marker that is essential for the maintenance of PSC self-renewal. : DSG2 is a desmosomal cadherin molecule. In this article, Min and colleagues show that DSG2 is a valuable PSC surface marker that is essential for the maintenance of PSC self-renewal and pluripotency and the acquisition of pluripotency during somatic cell reprogramming through the regulation of β-catenin-mediated EMT signaling. keywords: desmoglein-2, cell surface marker, pluripotent stem cells, monoclonal antibody, EMT