Identification of Alternatively Spliced Forms of human OSCAR in Osteoclasts
Korean Journal of Bone Metabolism
; : 11-20, 2012.
Article
ي En
| WPRIM
| ID: wpr-130875
المكتبة المسؤولة:
WPRO
ABSTRACT
OBJECTIVES: Osteoclasts are multinucleated giant cells which can resorb bone and differentiated from hematopoietic cells. We have previously reported murine osteoclast-associated receptor (OSCAR) may be an important bone-specific regulator of osteoclast differentiation. We have cloned soluble form of human OSCAR (hOSCAR) and examined the role of hOSCAR on osteoclast differentiation. METHODS: Osteoclast differentiation was induced by treatment with macrophage colony-stimulating factor (M-CSF) and receptor activator of nuclear factor kappa B ligand (RANKL) and tartrate-resistant acid phosphatase (TRAP) staining and pit formation were performed. Expression was measured by flow cytometry analysis, Northern and Western blot analysis. RESULTS: hOSCAR is expressed in osteoclast cells and involved in the differentiation of osteoclasts from peripheral blood mononuclear cells (PBMC). Two alternatively spliced forms (soluble hOSCAR [hOSCAR-S]) of hOSCAR were identified from osteoclasts complementary deoxyribonucleic acid (cDNA) library derived from PBMC. Putative transmembrane domain was not found in hOSCAR-S forms and it suggested that these forms might be secreted from osteoclast cells. These secreted forms of hOSCAR attenuated RANKL-induced osteoclast formation and bone resorption. CONCLUSIONS: Human osteoclasts express at least five different OSCAR messenger ribonucleic acid (mRNA) isoforms which could play different regulatory roles for differentiation. The secreted forms of hOSCAR might be a negative regulator of membrane-bounded forms of OSCAR.
Key words
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Osteoclasts
/
Acid Phosphatase
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DNA
/
RNA
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Giant Cells
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Blotting, Western
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Macrophage Colony-Stimulating Factor
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Clone Cells
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Alternative Splicing
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Protein Isoforms
نوع الدراسة:
Diagnostic_studies
/
Prognostic_studies
المحددات:
Humans
اللغة:
En
مجلة:
Korean Journal of Bone Metabolism
السنة:
2012
نوع:
Article