Park S H, Hsiao G Y-W, Huang G T-J
Division of Associated Clinical Specialties, Section of Endodontics, UCLA School of Dentistry, Los Angeles, CA 90095-1668, USA.
Int Endod J. 2004 Mar;37(3):185-92. doi: 10.1111/j.0143-2885.2004.00782.x.
To determine whether leucocyte infiltration during neurogenic inflammation in the pulp is regulated by neuropeptides via inducing the release of proinflammatory chemokines interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) from human dental pulp.
Cultured primary pulp cells and pulp tissue explants were stimulated with substance P (SP) and/or calcitonin gene-related peptide (CGRP). IL-8 or MCP-1, secreted from cultured cells or produced in pulp explants, was analysed by enzyme-linked immunosorbent assay.
Substance P induced IL-8 secretion from cultured pulp cells (approximately threefold increase over control, P < 0.05) and from pulp tissue explants (two- to three fold). SP only minimally to moderately induced MCP-1 (approximately two fold) in cultured pulp cells. While MCP-1 induction in cultured pulp cells was detected after 24 h of SP stimulation, no induction was observed in pulp tissue. CGRP did not induce IL-8, but moderately increased MCP-1 production (approximately three fold) in cultured pulp cells. There was no synergistic induction of MCP-1 by SP plus CGRP stimulation of pulp cells.
Substance P is a stronger inducer of IL-8 production in dental pulp than CGRP. IL-8 is more strongly induced than MCP-1 by SP, suggesting a more important role for IL-8 than MCP-1 in leucocyte infiltration during neurogenic inflammation in dental pulp.
确定牙髓神经源性炎症期间白细胞浸润是否由神经肽通过诱导人牙髓释放促炎趋化因子白细胞介素-8(IL-8)和单核细胞趋化蛋白-1(MCP-1)来调节。
用P物质(SP)和/或降钙素基因相关肽(CGRP)刺激原代培养的牙髓细胞和牙髓组织外植体。通过酶联免疫吸附测定法分析培养细胞分泌或牙髓外植体产生的IL-8或MCP-1。
P物质诱导培养的牙髓细胞分泌IL-8(比对照增加约三倍,P<0.05)以及牙髓组织外植体分泌IL-8(增加两到三倍)。SP仅轻微至中度诱导培养的牙髓细胞产生MCP-1(约两倍)。虽然在SP刺激24小时后检测到培养的牙髓细胞中有MCP-1的诱导,但在牙髓组织中未观察到诱导。CGRP不诱导IL-8,但适度增加培养的牙髓细胞中MCP-1的产生(约三倍)。SP加CGRP刺激牙髓细胞对MCP-1没有协同诱导作用。
在牙髓中,P物质比CGRP更能诱导IL-8的产生。SP对IL-8的诱导作用比对MCP-1更强,这表明在牙髓神经源性炎症期间,IL-8在白细胞浸润中比MCP-1发挥更重要的作用。