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Characterization of Binding and Phagocytosis of Oxidatively Damaged Erythrocyte to Macrophage

BACKGROUND: Scavenger receptors are thought to be involved in the recognition of oxidized low-density lipoprotein (oxLDL) and oxidized erythrocyte (oxRBC). However, there are controversies about the kind of receptors and ligands related to the binding. Macrophages lacking class A scavenger receptor...

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Autores principales: Ko, Hong Sook, Kim, In Seop, Lee, Kwangje, Kim, Sang Wook, Kim, Chee Jeong, Ryu, Wang Seong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531690/
https://www.ncbi.nlm.nih.gov/pubmed/12647635
http://dx.doi.org/10.3904/kjim.2002.17.4.220
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author Ko, Hong Sook
Kim, In Seop
Lee, Kwangje
Kim, Sang Wook
Kim, Chee Jeong
Ryu, Wang Seong
author_facet Ko, Hong Sook
Kim, In Seop
Lee, Kwangje
Kim, Sang Wook
Kim, Chee Jeong
Ryu, Wang Seong
author_sort Ko, Hong Sook
collection PubMed
description BACKGROUND: Scavenger receptors are thought to be involved in the recognition of oxidized low-density lipoprotein (oxLDL) and oxidized erythrocyte (oxRBC). However, there are controversies about the kind of receptors and ligands related to the binding. Macrophages lacking class A scavenger receptor show identical binding of oxRBC with wild-type ones. METHODS: RBCs were oxidized with ascorbic acid and CuSO(4). Lipid oxidation was measured indirectly by measuring TBARS semiquantitatively. The binding and phagocytosis were measured by counting the number of oxRBC bound or taken up after incubation at 4°C or 37°C for 60 minutes to 100 macrophages differentiated from human monocytic leukemia cell line. RESULTS: The degree of oxidation and the binding of oxRBCs were dependent on the concentration of CuSO(4). The binding and phagocytosis of oxRBC were inhibited by 99% with oxLDL. Fucoidan, competing class A scavenger receptor, inhibited the binding by more than 90%. The binding of oxRBC was higher at 37°C than at 4°C by 3 times. The binding of oxRBCs was maximal at pH 6.5 and higher than at physiologic pH by 2.8 times. At pH 8.5 and 9.5, binding decreased by 67 and 88%, respectively. CONCLUSION: OxRBCs might bind and be taken up to macrophages not mainly through class A nor B scavenger receptors, but through other scavenger receptors and/or pathways. These processes are dynamic and ionic strength might be involved.
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spelling pubmed-45316902015-10-02 Characterization of Binding and Phagocytosis of Oxidatively Damaged Erythrocyte to Macrophage Ko, Hong Sook Kim, In Seop Lee, Kwangje Kim, Sang Wook Kim, Chee Jeong Ryu, Wang Seong Korean J Intern Med Original Article BACKGROUND: Scavenger receptors are thought to be involved in the recognition of oxidized low-density lipoprotein (oxLDL) and oxidized erythrocyte (oxRBC). However, there are controversies about the kind of receptors and ligands related to the binding. Macrophages lacking class A scavenger receptor show identical binding of oxRBC with wild-type ones. METHODS: RBCs were oxidized with ascorbic acid and CuSO(4). Lipid oxidation was measured indirectly by measuring TBARS semiquantitatively. The binding and phagocytosis were measured by counting the number of oxRBC bound or taken up after incubation at 4°C or 37°C for 60 minutes to 100 macrophages differentiated from human monocytic leukemia cell line. RESULTS: The degree of oxidation and the binding of oxRBCs were dependent on the concentration of CuSO(4). The binding and phagocytosis of oxRBC were inhibited by 99% with oxLDL. Fucoidan, competing class A scavenger receptor, inhibited the binding by more than 90%. The binding of oxRBC was higher at 37°C than at 4°C by 3 times. The binding of oxRBCs was maximal at pH 6.5 and higher than at physiologic pH by 2.8 times. At pH 8.5 and 9.5, binding decreased by 67 and 88%, respectively. CONCLUSION: OxRBCs might bind and be taken up to macrophages not mainly through class A nor B scavenger receptors, but through other scavenger receptors and/or pathways. These processes are dynamic and ionic strength might be involved. Korean Association of Internal Medicine 2002-12 /pmc/articles/PMC4531690/ /pubmed/12647635 http://dx.doi.org/10.3904/kjim.2002.17.4.220 Text en Copyright © 2002 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ko, Hong Sook
Kim, In Seop
Lee, Kwangje
Kim, Sang Wook
Kim, Chee Jeong
Ryu, Wang Seong
Characterization of Binding and Phagocytosis of Oxidatively Damaged Erythrocyte to Macrophage
title Characterization of Binding and Phagocytosis of Oxidatively Damaged Erythrocyte to Macrophage
title_full Characterization of Binding and Phagocytosis of Oxidatively Damaged Erythrocyte to Macrophage
title_fullStr Characterization of Binding and Phagocytosis of Oxidatively Damaged Erythrocyte to Macrophage
title_full_unstemmed Characterization of Binding and Phagocytosis of Oxidatively Damaged Erythrocyte to Macrophage
title_short Characterization of Binding and Phagocytosis of Oxidatively Damaged Erythrocyte to Macrophage
title_sort characterization of binding and phagocytosis of oxidatively damaged erythrocyte to macrophage
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531690/
https://www.ncbi.nlm.nih.gov/pubmed/12647635
http://dx.doi.org/10.3904/kjim.2002.17.4.220
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