Comprehensive Cell Surface Antigen Analysis Identifies Transferrin Receptor Protein-1 (CD71) as a Negative Selection Marker for Human Neuronal Cells

Author:

Menon Vishal1234ORCID,Thomas Ria125,Elgueta Claudio6,Horl Marcus1,Osborn Teresia5,Hallett Penny J.5,Bartos Marlene6,Isacson Ole5,Pruszak Jan137ORCID

Affiliation:

1. Department of Molecular Embryology, Institute of Anatomy and Cell Biology, Faculty of Medicine, University of Freiburg, Freiburg, Germany

2. Spemann Graduate School of Biology and Medicine (SGBM) and Faculty of Biology, University of Freiburg, Freiburg, Germany

3. Freiburg iPS Core (FiPS), Institute for Transfusion Medicine and Gene Therapy, Medical Center, University of Freiburg, Freiburg, Germany

4. Faculty of Medicine, University of Freiburg, Freiburg, Germany

5. Neuroregeneration Laboratories, McLean Hospital, Harvard Medical School, Boston, Massachusetts, USA

6. Institute for Physiology I, Cellular and Systemic Neurophysiology, Faculty of Medicine, University of Freiburg, Freiburg, Germany

7. Center for Biological Signaling Studies (BIOSS), University of Freiburg, Freiburg, Germany

Abstract

Abstract Cell state-, developmental stage-, and lineage-specific combinatorial expression of cluster of differentiation (CD) molecules enables the identification of cellular subsets via multicolor flow cytometry. We describe an exhaustive characterization of neural cell types by surface antigens, exploiting human pluripotent stem cell-derived neural cell systems. Using multiwell screening approaches followed by detailed validation of expression patterns and dynamics, we exemplify a strategy for resolving cellular heterogeneity in stem cell paradigms. In addition to providing a catalog of surface antigens expressed in the neural lineage, we identified the transferrin receptor-1 (CD71) to be differentially expressed in neural stem cells and differentiated neurons. In this context, we describe a role for N-Myc proto-oncogene (MYCN) in maintaining CD71 expression in proliferating neural cells. We report that in vitro human stem cell-derived neurons lack CD71 surface expression and that the observed differential expression can be used to identify and enrich CD71− neuronal derivatives from heterogeneous cultures. Stem Cells  2019;37:1293–1306

Funder

Emmy Noether-Program of the German Research Foundation

DFG Excellence Initiative

scholarship funds from the State Graduate Funding Program of Baden-Württemberg

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

Reference62 articles.

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