Harokopakis Evlambia, Albzreh Mohamad H, Martin Michael H, Hajishengallis George
Center for Oral Health and Systemic Disease, University of Louisville Health Sciences Center, KY 40292, USA.
J Immunol. 2006 Jun 15;176(12):7645-56. doi: 10.4049/jimmunol.176.12.7645.
We present evidence for a novel TLR2 function in transmodulating the adhesive activities of human monocytes in response to the fimbriae of Porphyromonas gingivalis, a pathogen implicated in chronic periodontitis and atherosclerosis. Monocyte recruitment into the subendothelium is a crucial step in atherosclerosis, and we investigated the role of P. gingivalis fimbriae in stimulating monocyte adhesion to endothelial cells and transendothelial migration. Fimbriae induced CD11b/CD18-dependent adhesion of human monocytes or mouse macrophages to endothelial receptor ICAM-1; these activities were inhibited by TLR2 blockade or deficiency or by pharmacological inhibitors of PI3K. Moreover, this inducible adhesive activity was sensitive to the action of Clostridium difficile toxin B, but was not affected by Clostridium botulinum C3 exoenzyme, pertussis toxin, or cholera toxin. Accordingly, we subsequently showed through the use of dominant negative signaling mutants of small GTPases, that Rac1 mediates the ability of fimbria-stimulated monocytes to bind ICAM-1. A dominant negative mutant of Rac1 also inhibited the lipid kinase activity of PI3K suggesting that Rac1 acts upstream of PI3K in this proadhesive pathway. Furthermore, fimbriae stimulated monocyte adhesion to HUVEC and transmigration across HUVEC monolayers; both activities required TLR2 and Rac1 signaling and were dependent upon ICAM-1 and the high-affinity state of CD11b/CD18. P. gingivalis-stimulated monocytes displayed enhanced transendothelial migration compared with monocytes stimulated with nonfimbriated isogenic mutants. Thus, P. gingivalis fimbriae activate a novel proadhesive pathway in human monocytes, involving TLR2, Rac1, PI3K, and CD11b/CD18, which may constitute a mechanistic basis linking P. gingivalis to inflammatory atherosclerotic processes.
我们提供了证据,证明Toll样受体2(TLR2)具有一种新功能,即能反式调节人单核细胞的黏附活性,以响应牙龈卟啉单胞菌的菌毛,牙龈卟啉单胞菌是一种与慢性牙周炎和动脉粥样硬化有关的病原体。单核细胞募集到内皮下是动脉粥样硬化的关键步骤,我们研究了牙龈卟啉单胞菌菌毛在刺激单核细胞黏附于内皮细胞及跨内皮迁移中的作用。菌毛诱导人单核细胞或小鼠巨噬细胞通过CD11b/CD18依赖性方式黏附于内皮受体细胞间黏附分子-1(ICAM-1);这些活性可被TLR2阻断或缺陷,或PI3K的药理学抑制剂所抑制。此外,这种诱导性黏附活性对艰难梭菌毒素B的作用敏感,但不受肉毒梭菌C3外毒素、百日咳毒素或霍乱毒素的影响。因此,我们随后通过使用小GTP酶的显性负性信号突变体表明,Rac1介导了菌毛刺激的单核细胞结合ICAM-1的能力。Rac1的显性负性突变体也抑制了PI3K的脂质激酶活性,这表明在这条促黏附途径中Rac1作用于PI3K的上游。此外,菌毛刺激单核细胞黏附于脐静脉内皮细胞(HUVEC)并跨HUVEC单层迁移;这两种活性都需要TLR2和Rac1信号传导,并且依赖于ICAM-1和CD11b/CD18的高亲和力状态。与用无菌毛的同基因突变体刺激的单核细胞相比,牙龈卟啉单胞菌刺激的单核细胞表现出增强的跨内皮迁移。因此,牙龈卟啉单胞菌菌毛在人单核细胞中激活了一条新的促黏附途径,涉及TLR2、Rac1、PI3K和CD11b/CD18,这可能构成将牙龈卟啉单胞菌与炎症性动脉粥样硬化过程联系起来的机制基础。