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A glycan-based approach to cell characterization and isolation: Hematopoiesis as a paradigm
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 hem...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455685/ https://www.ncbi.nlm.nih.gov/pubmed/36066492 http://dx.doi.org/10.1084/jem.20212552 |
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author | Piszczatowski, Richard T. Schwenger, Emily Sundaravel, Sriram Stein, Catarina M. Liu, Yang Stanley, Pamela Verma, Amit Zheng, Deyou Seidel, Ronald D. Almo, Steven C. Townley, Robert A. Bülow, Hannes E. Steidl, Ulrich |
author_facet | Piszczatowski, Richard T. Schwenger, Emily Sundaravel, Sriram Stein, Catarina M. Liu, Yang Stanley, Pamela Verma, Amit Zheng, Deyou Seidel, Ronald D. Almo, Steven C. Townley, Robert A. Bülow, Hannes E. Steidl, Ulrich |
author_sort | Piszczatowski, Richard T. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9455685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94556852022-10-22 A glycan-based approach to cell characterization and isolation: Hematopoiesis as a paradigm Piszczatowski, Richard T. Schwenger, Emily Sundaravel, Sriram Stein, Catarina M. Liu, Yang Stanley, Pamela Verma, Amit Zheng, Deyou Seidel, Ronald D. Almo, Steven C. Townley, Robert A. Bülow, Hannes E. Steidl, Ulrich J Exp Med Article 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. Rockefeller University Press 2022-09-06 /pmc/articles/PMC9455685/ /pubmed/36066492 http://dx.doi.org/10.1084/jem.20212552 Text en © 2022 Piszczatowski et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Piszczatowski, Richard T. Schwenger, Emily Sundaravel, Sriram Stein, Catarina M. Liu, Yang Stanley, Pamela Verma, Amit Zheng, Deyou Seidel, Ronald D. Almo, Steven C. Townley, Robert A. Bülow, Hannes E. Steidl, Ulrich A glycan-based approach to cell characterization and isolation: Hematopoiesis as a paradigm |
title | A glycan-based approach to cell characterization and isolation: Hematopoiesis as a paradigm |
title_full | A glycan-based approach to cell characterization and isolation: Hematopoiesis as a paradigm |
title_fullStr | A glycan-based approach to cell characterization and isolation: Hematopoiesis as a paradigm |
title_full_unstemmed | A glycan-based approach to cell characterization and isolation: Hematopoiesis as a paradigm |
title_short | A glycan-based approach to cell characterization and isolation: Hematopoiesis as a paradigm |
title_sort | glycan-based approach to cell characterization and isolation: hematopoiesis as a paradigm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455685/ https://www.ncbi.nlm.nih.gov/pubmed/36066492 http://dx.doi.org/10.1084/jem.20212552 |
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