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cxcl-14 在大鼠磨牙胚萌出运动中的差异表达。

Differential expression of cxcl-14 during eruptive movement of rat molar germs.

机构信息

2nd Stage BK 21 for School of Dentistry, Dental Science Research Institute, Chonnam National University, Gwangju, South Korea.

出版信息

J Exp Zool B Mol Dev Evol. 2011 Sep 15;316(6):418-26. doi: 10.1002/jez.b.21414. Epub 2011 Apr 1.

Abstract

Tooth eruption at the early postnatal period is strictly controlled by the molecules secreted mainly from follicular tissues, which recruit monocytes for osteoclast formation. In this study, it was hypothesized that different molecules can be expressed according to the stages of tooth eruption. Rat molar germs together with follicles were extracted and DD-PCR was performed from the root formation stage 2nd molars germs (after eruptive movement) and cap stage 3rd molar germs (before movement) at postnatal day 9. Cxcl-14, a potent chemoattractant, was detected as one of the differentially expressed molecules from DD-PCR. Its expression increased significantly at the root formation stage, compared with the cap or crown formation stage at both transcription and translation levels. The expression patterns of cxcl-14 were consistent with those of MCP-1 and CSF-1, and opposite to OPG. Immunofluorescence showed that cxcl-14 was localized in the dental follicular tissues only at the root formation stage overlaying the proximo-occlusal region of the molar germs. Many osteoclasts appeared on the surface of the alveolar bone which overlayed the occlusal region of the root formation stage 2nd molar germs and underwent resorption. Cxcl-14 expression was reduced considerably at both the translation and transcription levels by an alendronate treatment. These results suggest that cxcl-14 may be implicated in the formation of the eruptive pathway of tooth germs via osteoclastogenesis.

摘要

牙齿在新生后早期的萌出受到来自滤泡组织的分子的严格调控,这些分子募集单核细胞形成破骨细胞。在本研究中,我们假设不同的分子可以根据牙齿萌出的阶段而表达。从新生后第 9 天的第 2 磨牙萌出运动后的根形成期和第 3 磨牙萌出前的帽状期牙胚中提取磨牙牙胚和滤泡,进行 DD-PCR。趋化因子 Cxcl-14 是一种有效的趋化因子,作为从 DD-PCR 差异表达的分子之一被检测到。其在转录和翻译水平上均在根形成期表达显著增加,与帽状期或牙冠形成期相比。cxcl-14 的表达模式与 MCP-1 和 CSF-1 的表达模式一致,与 OPG 的表达模式相反。免疫荧光显示,cxcl-14 仅在根形成期定位于覆盖磨牙牙胚近中-闭锁区的牙滤泡组织中。在根形成期第 2 磨牙牙胚的闭锁区上方的牙槽骨表面出现了许多破骨细胞,这些破骨细胞发生了吸收。阿仑膦酸盐处理后,cxcl-14 的翻译和转录水平均显著降低。这些结果表明,cxcl-14 可能通过破骨细胞形成参与了牙胚的萌出途径的形成。

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