| Literature DB >> 33741926 |
Robert N Barker1, Mark A Vickers2,3,4, Huan Cao1, Aristotelis Antonopoulos5, Sadie Henderson6, Heather Wassall1, John Brewin7, Alanna Masson8, Jenna Shepherd1, Gabriela Konieczny1, Bhinal Patel5, Maria-Louise Williams1, Adam Davie1, Megan A Forrester1, Lindsay Hall1, Beverley Minter1, Dimitris Tampakis9, Michael Moss6, Charlotte Lennon1, Wendy Pickford1, Lars Erwig1, Beverley Robertson5, Anne Dell7, Gordon D Brown1,10, Heather M Wilson1, David C Rees7, Stuart M Haslam5, J Alexandra Rowe11.
Abstract
In both sickle cell disease and malaria, red blood cells (RBCs) are phagocytosed in the spleen, but receptor-ligand pairs mediating uptake have not been identified. Here, we report that patches of high mannose N-glycans (Man5-9GlcNAc2), expressed on diseased or oxidized RBC surfaces, bind the mannose receptor (CD206) on phagocytes to mediate clearance. We find that extravascular hemolysis in sickle cell disease correlates with high mannose glycan levels on RBCs. Furthermore, Plasmodium falciparum-infected RBCs expose surface mannose N-glycans, which occur at significantly higher levels on infected RBCs from sickle cell trait subjects compared to those lacking hemoglobin S. The glycans are associated with high molecular weight complexes and protease-resistant, lower molecular weight fragments containing spectrin. Recognition of surface N-linked high mannose glycans as a response to cellular stress is a molecular mechanism common to both the pathogenesis of sickle cell disease and resistance to severe malaria in sickle cell trait.Entities:
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Year: 2021 PMID: 33741926 PMCID: PMC7979802 DOI: 10.1038/s41467-021-21814-z
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919