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PMID: 12553877 Published · ppublish English Journal Article

Expression and role of mannose receptor/terminal high-mannose type oligosaccharide on osteoclast precursors during osteoclast formation.

The Journal of endocrinology ·Vol. 176 ·No. 2 ·2003-02-00 ·Pages 285-92

Morishima S, Morita I, Tokushima T, Kawashima H, Miyasaka M, Omura K, Murota S

Abstract

Osteoclasts are formed from hematopoietic precursors via cell-cell fusion. We have previously reported that mannose residues are expressed on the outer membranes of monocytes during osteoclast differentiation. In the present study, we have attempted to demonstrate the pattern of expression levels of terminal high-mannose type oligosaccharide and to show that the mannose receptor is expressed on osteoclast precursor cells. Osteoclasts were formed using three different systems, namely mouse bone marrow cell culture, co-culture of mouse spleen cells with stromal cells, and RAW264.7 cell cultures. During osteoclast differentiation, the expression of terminal high-mannose type oligosaccharide gradually increased and then peaked at the stage of fusion in all three systems. Expression of the mannose receptor gradually increased during osteoclast differentiation in bone marrow cells and the co-culture system. In contrast, that in RAW264.7 cells had already been detected in the absence of the soluble receptor activator of NF-kappaB ligand and did not change during osteoclast differentiation. To ascertain whether expression of high-mannose type oligosaccharide is involved in tartrate-resistant acid phosphatase (TRAP)-positive multinucleated cell (MNC) formation, glycosidase inhibitors were used on RAW264.7 cell culture. Castanospermine, an inhibitor of glucosidase I, inhibited the TRAP-positive MNCs, and deoxymannojirimycin, an inhibitor of alpha-mannosidase I, increased the TRAP-positive MNC formation. These results indicate that the binding of terminal high-mannose and mannose receptor is important for the process of cellular fusion in osteoclast formation.

MeSH Terms
1-Deoxynojirimycin/pharmacology Acid Phosphatase/analysis Animals Biomarkers/analysis Bone Marrow Cells Cell Culture Techniques/methods Cell Differentiation/drug effects Cell Line Cells, Cultured Enzyme Inhibitors/pharmacology Glycoside Hydrolase Inhibitors Indolizines/pharmacology Isoenzymes/analysis Lectins, C-Type Macrophages/drug effects,metabolism Male Mannose Receptor Mannose-Binding Lectins Mannosidases/antagonists & inhibitors Mice Microscopy, Fluorescence Oligosaccharides/analysis,metabolism Osteoclasts/cytology,drug effects Receptors, Cell Surface/analysis,metabolism Stem Cells/cytology,drug effects Tartrate-Resistant Acid Phosphatase alpha-Glucosidases alpha-Mannosidase
Chemicals
Biomarkers Enzyme Inhibitors Glycoside Hydrolase Inhibitors Indolizines Isoenzymes Lectins, C-Type Mannose Receptor Mannose-Binding Lectins Oligosaccharides Receptors, Cell Surface 1-Deoxynojirimycin Acid Phosphatase Acp5 protein, mouse Tartrate-Resistant Acid Phosphatase Mannosidases glucosidase I alpha-Glucosidases alpha-Mannosidase castanospermine
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Morishima S
Cellular Physiological Chemistry, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo 113-8549, Japan.
Morita I
Tokushima T
Kawashima H
Miyasaka M
Omura K
Murota S
Article Info
Journal
The Journal of endocrinology
Abbr.
J Endocrinol
ISSN
0022-0795
Published
2003-02-00
Pages
285-92
Language
English
Region
England
NLM ID
0375363
Subset
IM
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