Liu Dawen, Yao Shaomian, Wise Gary E
Department of Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA.
Eur J Oral Sci. 2010 Aug;118(4):333-41. doi: 10.1111/j.1600-0722.2010.00751.x.
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.
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。