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Eryptotic Phenotype in Chronic Myeloid Leukemia: Contribution of Neutrophilic Cathepsin G
Author(s) -
Rukmini Govekar,
Poonam D. Kawle,
R. Brent Thomas,
Suresh H. Advani,
Sheena PV,
Surekha M. Zingde
Publication year - 2012
Publication title -
anemia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.921
H-Index - 25
eISSN - 2090-1275
pISSN - 2090-1267
DOI - 10.1155/2012/659303
Subject(s) - neutrophilia , cathepsin g , band 3 , myeloid leukemia , medicine , phenotype , immunology , leukemia , antigen , chronic myelogenous leukemia , biology , membrane protein , microbiology and biotechnology , genetics , gene , membrane , phosphorylation , serine
In pathological conditions with concurrent neutrophilia, modifications of erythrocyte membrane proteins are reported. In chronic myeloid leukemia (CML), a myeloproliferative disease wherein neutrophilia is accompanied by enhanced erythrophagocytosis, we report for the first time excessive cleavage of erythrocyte band 3. Distinct fragments of band 3 serve as senescent cell antigens leading to erythrophagocytosis. Using immunoproteomics, we report the identification of immunogenic 43 kDa fragment of band 3 in 68% of CML samples compared to their detection in only 38% of healthy individuals. Thus, excessive fragmentation of band 3 in CML, detected in our study, corroborated with the eryptotic phenotype. We demonstrate the role of neutrophilic cathepsin G, detected as an immunogen on erythrocyte membrane, in band 3 cleavage. Cathepsin G from serum adsorbs to the erythrocyte membrane to mediate cleavage of band 3 and therefore contribute to the eryptotic phenotype in CML.

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