| Literature DB >> 33547048 |
Anaïs Wanet1, Mahmoud A Bassal1,2, Sweta B Patel3, Francisco Marchi1, Samanta A Mariani4, Nouraiz Ahmed5, Haoran Zhang1, Marta Borchiellini6,7, Sisi Chen1, Junyan Zhang1, Annalisa Di Ruscio7,8,9, Kensuke Miyake10, Mindy Tsai11, Anuya Paranjape11, Shin-Young Park12, Hajime Karasuyama10, Timm Schroeder5, Elaine Dzierzak4, Stephen J Galli11,13, Daniel G Tenen14,2, Robert S Welner15.
Abstract
E-cadherin is a calcium-dependent cell-cell adhesion molecule extensively studied for its involvement in tissue formation, epithelial cell behavior, and suppression of cancer. However, E-cadherin expression in the hematopoietic system has not been fully elucidated. Combining single-cell RNA-sequencing analyses and immunophenotyping, we revealed that progenitors expressing high levels of E-cadherin and contained within the granulocyte-monocyte progenitors (GMPs) fraction have an enriched capacity to differentiate into basophils and mast cells. We detected E-cadherin expression on committed progenitors before the expression of other reported markers of these lineages. We named such progenitors pro-BMPs (pro-basophil and mast cell progenitors). Using RNA sequencing, we observed transcriptional priming of pro-BMPs to the basophil and mast cell lineages. We also showed that GATA-2 directly regulates E-cadherin expression in the basophil and mast cell lineages, thus providing a mechanistic connection between the expression of this cell surface marker and the basophil and mast cell fate specification.Entities:
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Year: 2021 PMID: 33547048 PMCID: PMC8261706 DOI: 10.1126/sciimmunol.aba0178
Source DB: PubMed Journal: Sci Immunol ISSN: 2470-9468