Induction of Calcitonin Receptors by 1 Alpha, 25-dihydroxyvitamin D3 in Osteoclast-like Multinucleated Cells Formed from Mouse Bone Marrow Cells
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We have developed a mouse marrow culture system, in which multinucleated cells (MNCs) are formed within 6-8 days. These MNCs showed several characteristics of osteoclasts, including tartrate-resistant acid phosphatase (TRACP) and the ability to resorb calcified dentine. 1 alpha, 25-Dihydroxyvitamin D3 [1 alpha, 25 (OH)2D3] stimulated the formation of TRACP-positive MNCs, and salmon calcitonin (CT) inhibited it. In this study, we examined whether the TRACP-positive MNCs formed from mouse marrow cells possess CT receptors, another typical characteristic of osteoclasts. Mouse marrow cells cultured for 8 days with 10 nM 1 alpha, 25(OH)2D3 and freshly isolated authentic mouse osteoclasts were incubated with [125I]-salmon CT in the presence or absence of excess amounts of unlabeled CT, stained for TRACP, and processed for autoradiography. The [125I]-CT exclusively bound to TRACP-positive mononuclear cells and MNCs formed in the 1 alpha, 25(OH)2D3-treated cultures and also to isolated mouse osteoclasts. Both [125I]-CT binding and TRACP activity were induced simultaneously on mononuclear cells on day 3 in the cultures treated with 1 alpha, 25(OH)2D3. CT markedly stimulated cAMP production in the 1 alpha,25(OH)2D3-treated cultures. The CT-dependent cAMP production increased in parallel with the increase in the number of TRACP-positive MNCs formed. Neither freshly isolated marrow cells nor cells cultured without 1 alpha, 25(OH)2D3 showed CT-induced cAMP accumulation. Furthermore, CT induced cytoplasmic contraction of both marrow-derived MNCs and isolated osteoclasts. These results clearly indicate that 1 alpha,25(OH)2D3 induces TRACP activity and CT receptors almost simultaneously in mouse marrow cultures, and the MNCs formed in vitro respond to CT as authentic osteoclasts do.
Wu Z, Deng W, Ye Y, Xu J, Han D, Zheng Y Front Endocrinol (Lausanne). 2024; 15:1378291.
PMID: 38868747 PMC: 11167098. DOI: 10.3389/fendo.2024.1378291.
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Shams R, Drasites K, Zaman V, Matzelle D, Shields D, Garner D Int J Mol Sci. 2021; 22(6).
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Historically significant events in the discovery of RANK/RANKL/OPG.
Martin T World J Orthop. 2013; 4(4):186-97.
PMID: 24147254 PMC: 3801238. DOI: 10.5312/wjo.v4.i4.186.
Aguila H, Mun S, Kalinowski J, Adams D, Lorenzo J, Lee S J Bone Miner Res. 2012; 27(5):1030-42.
PMID: 22258693 PMC: 3361560. DOI: 10.1002/jbmr.1553.
Martowicz M, Meyer M, Pike J J Cell Biochem. 2011; 112(8):2030-45.
PMID: 21465526 PMC: 3135786. DOI: 10.1002/jcb.23123.