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PMID: 1695609 Published · ppublish English Journal Article

Tissue distribution of HRF20, a novel factor preventing the membrane attack of homologous complement, and its predominant expression on endothelial cells in vivo.

Immunology ·Vol. 70 ·No. 2 ·1990-06-00 ·Pages 145-9

Nose M, Katoh M, Okada N, Kyogoku M, Okada H

Abstract

A 20,000 molecular weight (MW) homologous restriction factor (HRF20), detected by 1F5 monoclonal antibody (mAb), is present on blood cell surfaces and inhibits the terminal stage of the formation of membrane attack complexes by homologous complement activation. The tissue distribution of HRF20 was studied by immunohistochemical analysis using 1F5. HRF20 was predominantly expressed on endothelial cells of systemic arteries, veins and capillaries, as well as on the surface of cultured human umbilical vein endothelial cells. HRF20 was also detected, to a lesser extent, on the Schwann sheath of peripheral nerve fibres, ependymal cells and certain epithelial cells such as acinar cells of the salivary gland, bronchial epithelium, renal tubules and squamous epithelium. The distribution pattern of HRF20 differed somewhat from that of decay-accelerating factor (DAF), which is another membrane inhibitor of homologous complement activation.

MeSH Terms
Antibodies, Monoclonal Antigens, Differentiation/analysis CD59 Antigens Cells, Cultured Complement Membrane Attack Complex/biosynthesis Endothelium/analysis Endothelium, Vascular/analysis Epithelium/analysis Humans Immunoenzyme Techniques Membrane Glycoproteins/analysis Nervous System/analysis
Chemicals
Antibodies, Monoclonal Antigens, Differentiation CD59 Antigens Complement Membrane Attack Complex Membrane Glycoproteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Nose M
Department of Pathology, Tohoku University School of Medicine, Sendai, Japan.
Katoh M
Okada N
Kyogoku M
Okada H
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Article Info
Journal
Immunology
Abbr.
Immunology
ISSN
0019-2805
Published
1990-06-00
Pages
145-9
Language
English
Region
England
NLM ID
0374672
PMCID
PMC1384184
Subset
IM
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