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本文引用的文献

1
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.
2
MyD88 is required for protection from lethal infection with a mouse-adapted SARS-CoV.MyD88是抵御适应小鼠的严重急性呼吸综合征冠状病毒致死性感染所必需的。
PLoS Pathog. 2008 Dec;4(12):e1000240. doi: 10.1371/journal.ppat.1000240. Epub 2008 Dec 12.
3
MyD88 dependent signaling contributes to protective host defense against Burkholderia pseudomallei.依赖髓样分化因子88的信号传导有助于宿主对类鼻疽伯克霍尔德菌的保护性防御。
PLoS One. 2008;3(10):e3494. doi: 10.1371/journal.pone.0003494. Epub 2008 Oct 23.
4
Signaling through MyD88 regulates leukocyte recruitment after brain injury.通过髓样分化因子88(MyD88)进行的信号传导调节脑损伤后的白细胞募集。
J Immunol. 2008 Nov 1;181(9):6481-90. doi: 10.4049/jimmunol.181.9.6481.
5
TLR adaptor MyD88 is essential for pathogen control during oral toxoplasma gondii infection but not adaptive immunity induced by a vaccine strain of the parasite.Toll样受体衔接蛋白髓样分化因子88(MyD88)对于口腔感染刚地弓形虫期间的病原体控制至关重要,但对于该寄生虫疫苗株诱导的适应性免疫则并非必需。
J Immunol. 2008 Sep 1;181(5):3464-73. doi: 10.4049/jimmunol.181.5.3464.
6
Expression of endothelial monocyte-activating polypeptide II in the rat dental follicle and its potential role in tooth eruption.内皮单核细胞激活多肽II在大鼠牙囊中的表达及其在牙齿萌出中的潜在作用。
Eur J Oral Sci. 2008 Aug;116(4):334-40. doi: 10.1111/j.1600-0722.2008.00547.x.
7
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8
Attenuation of monocyte chemoattractant protein-1 expression via inhibition of nuclear factor-kappaB activity in inflammatory vascular injury.通过抑制核因子-κB活性减轻炎症性血管损伤中单核细胞趋化蛋白-1的表达
Am J Hypertens. 2007 Nov;20(11):1170-5. doi: 10.1016/j.amjhyper.2007.07.011.
9
A DNA microarray analysis of chemokine and receptor genes in the rat dental follicle--role of secreted frizzled-related protein-1 in osteoclastogenesis.大鼠牙囊趋化因子和受体基因的DNA微阵列分析——分泌型卷曲相关蛋白-1在破骨细胞生成中的作用
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10
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大鼠牙囊中的髓样分化因子88表达:对破骨细胞生成和牙齿萌出的影响

MyD88 expression in the rat dental follicle: implications for osteoclastogenesis and tooth eruption.

作者信息

Liu Dawen, Yao Shaomian, Wise Gary E

机构信息

Department of Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA.

出版信息

Eur J Oral Sci. 2010 Aug;118(4):333-41. doi: 10.1111/j.1600-0722.2010.00751.x.

DOI:10.1111/j.1600-0722.2010.00751.x
PMID:20662905
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2914338/
Abstract

Myeloid differentiation factor 88 (MyD88) is a key adaptor molecule in the interleukin (IL)-1 and IL-18 toll-like receptor signaling pathways. Because MyD88 is present in dental follicle (DF) cells in vitro, the purpose of this study was to determine its chronological expression in vivo, as well as its possible role in osteoclastogenesis and tooth eruption. An oligo DNA microarray was used to determine expression of the Myd88 gene in vivo in the DFs from the first mandibular molars of postnatal rats from days 1 to 11. The results showed that MyD88 was expressed maximally on day 3. Using small interfering RNA (siRNA) to knock down MyD88 expression in the DF cells also reduced the expression of the nuclear factor-kappa B-1 (NFKB1) and monocyte chemoattractant protein 1 (MCP-1) genes. Interleukin-1alpha up-regulated the expression of NFKB1, MCP-1, and receptor activator of nuclear factor kappa B ligand (RANKL), but knockdown of MyD88 nullified this IL-1alpha effect. Conditioned medium from DF cells with MyD88 knocked down had reduced chemotactic activity for mononuclear cells and reduced osteoclastogenesis, as opposed to controls. In conclusion, the maximal expression of MyD88 in the DF of postnatal day 3 rats may contribute to the major burst of osteoclastogenesis needed for eruption by up-regulating MCP-1 and RANKL expression.

摘要

髓样分化因子88(MyD88)是白细胞介素(IL)-1和IL-18Toll样受体信号通路中的关键衔接分子。由于体外培养的牙囊(DF)细胞中存在MyD88,本研究旨在确定其在体内的时序表达,以及其在破骨细胞生成和牙齿萌出中的可能作用。利用寡核苷酸DNA微阵列检测出生后1至11天大鼠下颌第一磨牙DF中Myd88基因的体内表达。结果显示,MyD88在出生后第3天表达最高。使用小干扰RNA(siRNA)敲低DF细胞中MyD88的表达,也降低了核因子-κB-1(NFKB1)和单核细胞趋化蛋白1(MCP-1)基因的表达。白细胞介素-1α上调了NFKB1、MCP-1和核因子κB受体激活剂配体(RANKL)的表达,但敲低MyD88可消除白细胞介素-1α的这种作用。与对照组相比,敲低MyD88的DF细胞条件培养基对单核细胞的趋化活性降低,破骨细胞生成减少。总之,出生后第3天大鼠DF中MyD88的最高表达可能通过上调MCP-1和RANKL的表达,促进萌出所需的破骨细胞生成的主要爆发。