Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/27535
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Type: Journal article
Title: MHC class II compartment, endocytosis and phagocytic activity of macrophages and putative dendritic cells isolated from normal tissues rich in synovium
Author: Moghaddami, M.
Mayrhofer, G.
Cleland, L.
Citation: International Immunology, 2005; 17(8):1117-1130
Publisher: Oxford Univ Press
Issue Date: 2005
ISSN: 0953-8178
1460-2377
Abstract: The endocytic and phagocytic activities of a population of MHC IIhi CD11c+ dendritic cell (DC)-like cells in synovium-rich tissues (SRTs) of normal rat paws were compared with CD163+ cells (putative macrophages) from the same tissues and pseudo-afferent lymph DCs, peritoneal macrophages and blood monocytes. Fifty percent of CD11c+ cells and 75% of CD163+ cells isolated from SRT internalized fluorescein-conjugated dextran (FITC-DX). Of these endocytic cells, half of those expressing CD11c, but only 30% of those expressing CD163, were surface MHC class II+ (sMHC II+). CD11c+ cells were more endocytic than monocytes or pseudo-afferent lymph DC, but some CD163+ cells (type A synoviocytes) were found to be highly endocytic. CD163+ cells from SRT were more phagocytic (25%) than the general MHC class II+ population (16%). Of phagocytic cells, 40% of CD163+ cells were sMHC IIvariable and they constituted 60% of all MHC class II+ phagocytic cells. Only 18% of phagocytic MHC II+ cells expressed CD11c and the most of these were MHC IIhi. In comparison, 60% of CD163+ peritoneal macrophages were phagocytic, while blood monocytes were poorly phagocytic. Intracellular MHC class II-rich compartments (MIIC) were prominent in sMHC IIhi cells in SRT but rare in CD163+ cells. Most MHC IIhi CD11c+ cells did not have a detectable MIIC.
Keywords: antigen-presenting cells
endocytosis
MIIC
phagocytosis
synovial cells
Description: Copyright © 2005 Japanese Society for Immunology
DOI: 10.1093/intimm/dxh291
Published version: http://intimm.oxfordjournals.org/cgi/content/abstract/17/8/1117
Appears in Collections:Aurora harvest 6
Molecular and Biomedical Science publications

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