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细胞培养中碳酸磷灰石板上的破骨细胞和成骨细胞活性。

Osteoclast and osteoblast activities on carbonate apatite plates in cell cultures.

机构信息

Department of Periodontology, Division of Oral Infections and Health Science, Asahi University School of Dentistry, 1851, Hozumi, Mizuho, Gifu 501-0296, Japan.

出版信息

J Biomater Appl. 2011 Nov;26(4):435-49. doi: 10.1177/0885328210374672. Epub 2010 Jul 12.

Abstract

Previous studies have demonstrated that carbonate apatite (CA) is superior to hydroxyapatite (HA) and β-tricalciumphosphate (β-TCP) with regard to osteoclastic resorption, but evidence on osteoclast and osteoblast response remains controversial. In the present study, the expression of bone related mRNA is examined on CA, HA, β-TCP, and titanium plates. ICR mouse osteoblast cells are cocultured with ICR mouse bone marrow cells. Crude osteoclast-like cell-rich suspensions are then seeded onto plates and cultured for 48 h. Total RNA is extracted and mRNA expression is examined by real-time RT-PCR. Amounts of vacuolar-type ATPase, cathepsin K, and TRAP mRNA are significantly greater on CA than on the other plates. The amount of osteoprotegerin mRNA is significantly greater on CA than on the other plates. RANKL mRNA expression, which is generally regarded as an osteoblast maker, varies with material, but shows no significant differences between CA and the other plates. The formation and activity of osteoclasts is greater with CA than with the other plates. Thus, CA is superior to β-TCP as a bioresorbable bone substitute for tissue engineering.

摘要

先前的研究表明,在破骨细胞吸收方面,碳酸磷灰石(CA)优于羟基磷灰石(HA)和β-磷酸三钙(β-TCP),但关于破骨细胞和成骨细胞反应的证据仍存在争议。在本研究中,我们研究了 CA、HA、β-TCP 和钛板上与骨相关的 mRNA 的表达。ICR 小鼠成骨细胞与 ICR 小鼠骨髓细胞共培养。然后将粗破骨细胞样细胞丰富的悬浮液接种到平板上,并培养 48 小时。提取总 RNA,并通过实时 RT-PCR 检查 mRNA 表达。与其他平板相比,CA 上的液泡型 ATP 酶、组织蛋白酶 K 和 TRAP mRNA 的量显著更高。CA 上的护骨素 mRNA 量明显高于其他平板。通常被认为是成骨细胞标志物的 RANKL mRNA 表达随材料而异,但 CA 与其他平板之间没有显著差异。与其他平板相比,CA 上破骨细胞的形成和活性更大。因此,CA 作为组织工程的可生物吸收骨替代物优于 β-TCP。

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