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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/33268
Title: Glycophorin C (CD236R) mediates vivax malaria parasite rosetting to normocytes
Authors: Wenn Chyau Lee
Benoit Malleret
Yee Ling Lau
Marjorie Mauduit
Mun Yik Fong
Jee Sun Cho
Rossarin Suwanarusk
Rou Zhang
Letusa Albrecht
Fabio T M Costa
Peter Preiser
Rose McGready
Laurent Renia
Francois Nosten
Bruce Russell
University of Malaya
National University of Singapore
Agency for Science, Technology and Research, Singapore
Universidade Estadual de Campinas
Nanyang Technological University
Mahidol University
Nuffield Department of Clinical Medicine
Keywords: Biochemistry, Genetics and Molecular Biology;Immunology and Microbiology;Medicine
Issue Date: 1-May-2014
Citation: Blood. Vol.123, No.18 (2014)
Abstract: Rosetting phenomenon has been linked to malaria pathogenesis. Although rosetting occurs in all causes of human malaria, most data on this subject has been derived from Plasmodium falciparum. Here, we investigate the function and factors affecting rosette formation in Plasmodiumvivax. To achieve this, we used a range of novel ex vivo protocols to study fresh and cryopreserved P vivax (n5 135) and P falciparum(n5 77) isolates from Thailand. Rosetting is more common in vivax than falciparum malaria, both in terms of incidence in patient samples and percentage of infected erythrocytes forming rosettes. Rosetting to P vivax asexual and sexual stages was evident 20 hours postreticulocyte invasion, reaching a plateau after 30 hours. Host ABOblood group, reticulocyte count, and parasitemia were not correlated with P vivax rosetting. Importantly, mature erythrocytes (normocytes), rather than reticulocytes, preferentially form rosetting complexes, indicating that this process is unlikely to directly facilitate merozoite invasion. Although antibodies against host erythrocyte receptors CD235a and CD35 had no effect, Ag-binding fragment against the BRIC 4 region of CD236R significantly inhibited rosette formation. Rosetting assays using CD236R knockdown normocytes derived from hematopoietic stem cells further supports the role of glycophorin C as a receptor in P vivax rosette formation. © 2014 by The American Society of Hematology.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84900440031&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/33268
ISSN: 15280020
00064971
Appears in Collections:Scopus 2011-2015

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