Botero Tatiana M, Shelburne Charles E, Holland G Rex, Hanks Carl T, Nör Jacques E
Department of Cariology, Restorative Sciences and Endodontics, University of Michigan, School of Dentistry, Ann Arbor, Michigan 48109-1078, USA.
J Endod. 2006 Oct;32(10):951-5. doi: 10.1016/j.joen.2006.03.018. Epub 2006 Jul 26.
Lipopolysaccharide (LPS) from gram-negative bacteria cell walls such as Prevotella intermedia and Escherichia coli induce vascular endothelial growth factor (VEGF) expression in odontoblasts, but not in undifferentiated dental pulp cells. CD14 and TLR4 are responsible for LPS signaling in macrophages, but their expression levels and function in dental pulp cells are unknown. We showed here that murine odontoblast-like cells (MDPC-23) express CD14 and TLR4 by immunohistochemistry and flow cytometry. In contrast, undifferentiated dental pulp cells (OD-21) presented low or no expression of these two receptors. MDPC-23 cells showed CD14 and TLR4 up-regulation upon exposure to LPS, as determined by real time PCR. Dominant negative murine TLR4 (DN-mTLR4) transfected MDPC-23 cells did not show upregulated VEGF expression in response to LPS stimulation. These results demonstrate that odontoblast-like cells express CD14 and TLR4, and that LPS-induced VEGF expression is mediated, at least in part, by TLR4 signaling.
来自革兰氏阴性菌细胞壁的脂多糖(LPS),如中间普氏菌和大肠杆菌,可诱导成牙本质细胞表达血管内皮生长因子(VEGF),但未分化的牙髓细胞则不会。CD14和TLR4负责巨噬细胞中的LPS信号传导,但其在牙髓细胞中的表达水平和功能尚不清楚。我们在此表明,通过免疫组织化学和流式细胞术,小鼠成牙本质细胞样细胞(MDPC-23)表达CD14和TLR4。相比之下,未分化的牙髓细胞(OD-21)这两种受体的表达较低或无表达。实时PCR检测显示,MDPC-23细胞在暴露于LPS后CD14和TLR4上调。转染显性负性小鼠TLR4(DN-mTLR4)的MDPC-23细胞在LPS刺激下未出现VEGF表达上调。这些结果表明,成牙本质细胞样细胞表达CD14和TLR4,且LPS诱导的VEGF表达至少部分由TLR4信号传导介导。