Dunzendorfer Stefan, Lee Hyun-Ku, Soldau Katrin, Tobias Peter S
Department of Immunology, The Scripps Research Institute, La Jolla, CA 92037, USA.
J Immunol. 2004 Jul 15;173(2):1166-70. doi: 10.4049/jimmunol.173.2.1166.
TLR4 is the primary recognition molecule for inflammatory responses initiated by bacterial LPS (endotoxin). Internalization of endotoxin by various cell types is an important step for its removal and detoxification. Because of its role as an LPS-signaling receptor, TLR4 has been suggested to be involved in cellular LPS uptake as well. LPS uptake was investigated in primary monocytes and endothelial cells derived from TLR4 and CD14 knockout C57BL/6 mice using tritiated and fluorescein-labeled LPS. Intracellular LPS distribution was investigated by deconvolution confocal microscopy. We could not observe any difference in LPS uptake and intracellular LPS distribution in either monocytes or endothelial cells between TLR4(-/-) and wild-type cells. As expected, CD14(-/-) monocytes showed a highly impaired LPS uptake, confirming CD14-dependent uptake in monocytes. Upon longer incubation periods, the CD14-deficient monocytes mimicked the LPS uptake pattern of endothelial cells. Endothelial cell LPS uptake is slower than monocyte uptake, LBP rather than CD14 dependent, and sensitive to polyanionic polymers, which have been shown to block scavenger receptor-dependent uptake mechanisms. We conclude that TLR4 is not involved in cellular LPS uptake mechanisms. In membrane CD14-positive cells, LPS is predominantly taken up via CD14-mediated pathways, whereas in the CD14-negative endothelial cells, there is a role for scavenger receptor-dependent pathways.
Toll样受体4(TLR4)是由细菌脂多糖(内毒素)引发的炎症反应的主要识别分子。各种细胞类型对内毒素的内化作用是内毒素清除和解毒的重要步骤。由于TLR4作为脂多糖信号受体的作用,也有人提出它参与细胞对脂多糖的摄取。使用氚标记和荧光素标记的脂多糖,对源自TLR4和CD14基因敲除的C57BL/6小鼠的原代单核细胞和内皮细胞中的脂多糖摄取情况进行了研究。通过去卷积共聚焦显微镜研究细胞内脂多糖的分布。我们在TLR4基因敲除(-/-)细胞和野生型细胞的单核细胞或内皮细胞中均未观察到脂多糖摄取及细胞内脂多糖分布存在任何差异。正如预期的那样,CD14基因敲除(-/-)的单核细胞显示出脂多糖摄取能力严重受损,证实了单核细胞中脂多糖摄取依赖于CD14。在较长的孵育期后,缺乏CD14的单核细胞模仿了内皮细胞的脂多糖摄取模式。内皮细胞对脂多糖的摄取比单核细胞慢,依赖于脂多糖结合蛋白(LBP)而非CD14,并且对多阴离子聚合物敏感,多阴离子聚合物已被证明可阻断清道夫受体依赖性摄取机制。我们得出结论,TLR4不参与细胞对脂多糖的摄取机制。在膜CD14阳性细胞中,脂多糖主要通过CD14介导的途径摄取,而在CD14阴性的内皮细胞中,清道夫受体依赖性途径发挥作用。