A glycan-based approach to cell characterization and isolation: Hematopoiesis as a paradigm

Author:

Piszczatowski Richard T.1ORCID,Schwenger Emily1ORCID,Sundaravel Sriram1ORCID,Stein Catarina M.2ORCID,Liu Yang2ORCID,Stanley Pamela13ORCID,Verma Amit45367ORCID,Zheng Deyou289ORCID,Seidel Ronald D.10ORCID,Almo Steven C.103ORCID,Townley Robert A.2106ORCID,Bülow Hannes E.283ORCID,Steidl Ulrich153711ORCID

Affiliation:

1. Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 1

2. Department of Genetics, Albert Einstein College of Medicine, Bronx, NY 2

3. Montefiore Einstein Cancer Center, Albert Einstein College of Medicine-Montefiore Health System, Bronx, NY 7

4. Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 4

5. Departments of Oncology and Medicine, Albert Einstein College of Medicine-Montefiore Health System, Bronx, NY 6

6. Department of Biological Sciences, University of Wisconsin Milwaukee, Milwaukee, WI 8

7. Blood Cancer Institute, Albert Einstein College of Medicine, Bronx, NY 9

8. Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 5

9. 10The Saul R. Korey Department of Neurology, Albert Einstein College of Medicine, Bronx, NY

10. Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 3

11. Ruth L. and David S. Gottesman Institute for Stem Cell Research and Regenerative Medicine, Albert Einstein College of Medicine, Bronx, NY 11

Abstract

Cell surfaces display a wide array of molecules that confer identity. While flow cytometry and cluster of differentiation (CD) markers have revolutionized cell characterization and purification, functionally heterogeneous cellular subtypes remain unresolvable by the CD marker system alone. Using hematopoietic lineages as a paradigm, we leverage the extraordinary molecular diversity of heparan sulfate (HS) glycans to establish cellular “glycotypes” by utilizing a panel of anti-HS single-chain variable fragment antibodies (scFvs). Prospective sorting with anti-HS scFvs identifies functionally distinct glycotypes within heterogeneous pools of mouse and human hematopoietic progenitor cells and enables further stratification of immunophenotypically pure megakaryocyte–erythrocyte progenitors. This stratification correlates with expression of a heptad of HS-related genes that is reflective of the HS epitope recognized by specific anti-HS scFvs. While we show that HS glycotyping provides an orthogonal set of tools for resolution of hematopoietic lineages, we anticipate broad utility of this approach in defining and isolating novel, viable cell types across diverse tissues and species.

Funder

NYSTEM

National Institutes of Health

Medical Scientist Training Programs

National Cancer Institute

Jane A. and Myles P. Dempsey

Wollowick Family Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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