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本文引用的文献

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Electroporation to deliver plasmid DNA into rat dental tissues.电穿孔将质粒 DNA 递送入大鼠牙组织。
J Gene Med. 2010 Dec;12(12):981-9. doi: 10.1002/jgm.1521.
2
Cellular and molecular basis of tooth eruption.牙齿萌出的细胞和分子基础。
Orthod Craniofac Res. 2009 May;12(2):67-73. doi: 10.1111/j.1601-6343.2009.01439.x.
3
Mechanisms of tooth eruption and orthodontic tooth movement.牙齿萌出与正畸牙齿移动的机制。
J Dent Res. 2008 May;87(5):414-34. doi: 10.1177/154405910808700509.
4
Osteogenic gene expression by human periodontal ligament cells under cyclic tension.人牙周膜细胞在周期性张力作用下的成骨基因表达
J Dent Res. 2007 Dec;86(12):1212-6. doi: 10.1177/154405910708601214.
5
Impaired growth plate function in bmp-6 null mice.骨形态发生蛋白-6基因敲除小鼠生长板功能受损。
Bone. 2008 Jan;42(1):216-25. doi: 10.1016/j.bone.2007.09.053. Epub 2007 Oct 4.
6
Bone morphogenetic proteins and their receptors in the eye.眼部的骨形态发生蛋白及其受体
Exp Biol Med (Maywood). 2007 Sep;232(8):979-92. doi: 10.3181/0510-MR-345.
7
Bone formation as a potential motive force of tooth eruption in the rat molar.骨形成作为大鼠磨牙牙齿萌出的潜在驱动力。
Clin Anat. 2007 Aug;20(6):632-9. doi: 10.1002/ca.20495.
8
Gradients in bone morphogenetic protein-related gene expression across the growth plate.生长板中骨形态发生蛋白相关基因表达的梯度变化。
J Endocrinol. 2007 Apr;193(1):75-84. doi: 10.1677/joe.1.07099.
9
Regional differences of expression of bone morphogenetic protein-2 and RANKL in the rat dental follicle.大鼠牙囊骨形态发生蛋白-2和RANKL表达的区域差异
Eur J Oral Sci. 2006 Dec;114(6):512-6. doi: 10.1111/j.1600-0722.2006.00406.x.
10
CSF-1 regulation of osteoclastogenesis for tooth eruption.集落刺激因子-1对牙齿萌出过程中破骨细胞生成的调节作用。
J Dent Res. 2005 Sep;84(9):837-41. doi: 10.1177/154405910508400911.

大鼠磨牙萌出对牙槽骨形成的需求。

Requirement of alveolar bone formation for eruption of rat molars.

作者信息

Wise Gary E, He Hongzhi, Gutierrez Dina L, Ring Sherry, Yao Shaomian

机构信息

Department of Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, USA.

出版信息

Eur J Oral Sci. 2011 Oct;119(5):333-8. doi: 10.1111/j.1600-0722.2011.00854.x.

DOI:10.1111/j.1600-0722.2011.00854.x
PMID:21896048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3170088/
Abstract

Tooth eruption is a localized event that requires a dental follicle (DF) to regulate the resorption of alveolar bone to form an eruption pathway. During the intra-osseous phase of eruption, the tooth moves through this pathway. The mechanism or motive force that propels the tooth through this pathway is controversial but many studies have shown that alveolar bone growth at the base of the crypt occurs during eruption. To determine if this bone growth (osteogenesis) was causal, experiments were designed in which the expression of an osteogenic gene in the DF, bone morphogenetic protein-6 (Bmp6), was inhibited by injection of the first mandibular molar of the rat with a small interfering RNA (siRNA) targeted against Bmp6. The injection was followed by electroporation to promote uptake of the siRNA. In 45 first molars injected, eruption was either delayed or completely inhibited (seven molars). In the impacted molars, an eruption pathway formed but bone growth at the base of the crypt was greatly reduced compared with the erupted first-molar controls. These studies show that alveolar bone growth at the base of the crypt is required for tooth eruption and that Bmp6 may be essential for promoting this growth.

摘要

牙齿萌出是一个局部性事件,需要牙囊(DF)调节牙槽骨的吸收以形成萌出通道。在萌出的骨内阶段,牙齿通过该通道移动。推动牙齿通过该通道的机制或动力存在争议,但许多研究表明,在萌出过程中,隐窝底部的牙槽骨会生长。为了确定这种骨生长(成骨作用)是否具有因果关系,设计了实验,通过向大鼠的第一下颌磨牙注射针对骨形态发生蛋白-6(Bmp6)的小干扰RNA(siRNA)来抑制DF中成骨基因的表达。注射后进行电穿孔以促进siRNA的摄取。在45颗注射的第一磨牙中,萌出要么延迟要么完全被抑制(7颗磨牙)。在阻生磨牙中,形成了萌出通道,但与已萌出的第一磨牙对照相比,隐窝底部的骨生长大大减少。这些研究表明,隐窝底部的牙槽骨生长是牙齿萌出所必需的,并且Bmp6可能对促进这种生长至关重要。