Constitutive and inducible expression of HLA class II determinants by human osteoblast-like cells in vitro

Activated immune cells release cytokines which modulate the activity of bone cells in vitro. Expression of major histocompatibility complex (HLA in humans) class II determinants on bone surface cells may be important in local immune cell activation. In this study, expression of HLA-DR and DQ by cult...

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Veröffentlicht in:The Journal of clinical investigation 1990-05, Vol.85 (5), p.1421-1426
Hauptverfasser: SKJØDT, H, HUGHES, D. E, DOBSON, P. R. M, RUSSELL, R. G. G
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container_issue 5
container_start_page 1421
container_title The Journal of clinical investigation
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creator SKJØDT, H
HUGHES, D. E
DOBSON, P. R. M
RUSSELL, R. G. G
description Activated immune cells release cytokines which modulate the activity of bone cells in vitro. Expression of major histocompatibility complex (HLA in humans) class II determinants on bone surface cells may be important in local immune cell activation. In this study, expression of HLA-DR and DQ by cultured human bone cells (HBC) derived from normal trabecular bone surfaces was assessed by fluorescence-activated cell sorter (FACS) analysis and immunoperoxidase techniques using monoclonal antibodies. A subset of HBC (10-30%) expressed DR constitutively while 5-15% displayed DQ during long-term culture. HBC lacked a number of monocyte and lymphocyte markers. In addition, both DR+ and DR- HBC (FACS separated) produced osteocalcin stimulated by 1,25-dihydroxyvitamin D2 (1,25(OH)2D3). This suggests that both phenotypes belong to the osteoblast lineage. The number of DR+ HBC was increased by interferon-gamma (IFN gamma; 40-95% DR+ cells) whereas DQ+ HBC remained unchanged or was slightly increased (5-20% DQ+ cells). Moreover, 1,25(OH)2D3 enhanced IFN gamma-induced DR expression and at high concentration (10(-7) M) augmented DR expression by itself. Other major osteotropic factors, parathyroid hormone, interleukin 1, and calcitonin, did not affect HBC DR expression. The findings suggest that HBC may participate in activation of the immune system and that some osteotropic factors may regulate this function.
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E</creatorcontrib><creatorcontrib>DOBSON, P. R. M</creatorcontrib><creatorcontrib>RUSSELL, R. G. G</creatorcontrib><title>Constitutive and inducible expression of HLA class II determinants by human osteoblast-like cells in vitro</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>Activated immune cells release cytokines which modulate the activity of bone cells in vitro. Expression of major histocompatibility complex (HLA in humans) class II determinants on bone surface cells may be important in local immune cell activation. In this study, expression of HLA-DR and DQ by cultured human bone cells (HBC) derived from normal trabecular bone surfaces was assessed by fluorescence-activated cell sorter (FACS) analysis and immunoperoxidase techniques using monoclonal antibodies. A subset of HBC (10-30%) expressed DR constitutively while 5-15% displayed DQ during long-term culture. HBC lacked a number of monocyte and lymphocyte markers. In addition, both DR+ and DR- HBC (FACS separated) produced osteocalcin stimulated by 1,25-dihydroxyvitamin D2 (1,25(OH)2D3). This suggests that both phenotypes belong to the osteoblast lineage. The number of DR+ HBC was increased by interferon-gamma (IFN gamma; 40-95% DR+ cells) whereas DQ+ HBC remained unchanged or was slightly increased (5-20% DQ+ cells). Moreover, 1,25(OH)2D3 enhanced IFN gamma-induced DR expression and at high concentration (10(-7) M) augmented DR expression by itself. Other major osteotropic factors, parathyroid hormone, interleukin 1, and calcitonin, did not affect HBC DR expression. 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G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Constitutive and inducible expression of HLA class II determinants by human osteoblast-like cells in vitro</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>1990-05-01</date><risdate>1990</risdate><volume>85</volume><issue>5</issue><spage>1421</spage><epage>1426</epage><pages>1421-1426</pages><issn>0021-9738</issn><eissn>1558-8238</eissn><coden>JCINAO</coden><abstract>Activated immune cells release cytokines which modulate the activity of bone cells in vitro. Expression of major histocompatibility complex (HLA in humans) class II determinants on bone surface cells may be important in local immune cell activation. In this study, expression of HLA-DR and DQ by cultured human bone cells (HBC) derived from normal trabecular bone surfaces was assessed by fluorescence-activated cell sorter (FACS) analysis and immunoperoxidase techniques using monoclonal antibodies. A subset of HBC (10-30%) expressed DR constitutively while 5-15% displayed DQ during long-term culture. HBC lacked a number of monocyte and lymphocyte markers. In addition, both DR+ and DR- HBC (FACS separated) produced osteocalcin stimulated by 1,25-dihydroxyvitamin D2 (1,25(OH)2D3). This suggests that both phenotypes belong to the osteoblast lineage. The number of DR+ HBC was increased by interferon-gamma (IFN gamma; 40-95% DR+ cells) whereas DQ+ HBC remained unchanged or was slightly increased (5-20% DQ+ cells). Moreover, 1,25(OH)2D3 enhanced IFN gamma-induced DR expression and at high concentration (10(-7) M) augmented DR expression by itself. 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subjects Adult
Aged
Biological and medical sciences
Bone and Bones - immunology
Calcitonin - pharmacology
Calcitriol - pharmacology
Cells, Cultured
Cycloheximide - pharmacology
Female
Histocompatibility Antigens Class II - genetics
HLA-DQ Antigens - analysis
HLA-DQ Antigens - genetics
HLA-DR Antigens - analysis
HLA-DR Antigens - genetics
Humans
Immunopathology
Interferon-gamma - pharmacology
Interleukin-1 - pharmacology
Kinetics
Male
Medical sciences
Middle Aged
Osteoblasts - drug effects
Osteoblasts - immunology
Osteocalcin - biosynthesis
Parathyroid Hormone - pharmacology
Recombinant Proteins
title Constitutive and inducible expression of HLA class II determinants by human osteoblast-like cells in vitro
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