Marchant A, Duchow J, Delville J P, Goldman M
Department of Immunology, Hôpital Erasme, Université Libre de Bruxelles, Belgium.
Eur J Immunol. 1992 Jun;22(6):1663-5. doi: 10.1002/eji.1830220650.
We examined by flow cytometry the expression of lipopolysaccharide (LPS) receptor CD14 molecule on monocytes after addition of LPS to human whole blood. Within 30 min LPS induced an increase in monocyte CD14 expression, peaking between 1 and 3 h and followed by a slow decrease. Maximal increase in anti-CD14 monoclonal antibody binding sites was estimated as twofold the basal value. This effect, already observed with very low concentrations of LPS (10 pg/ml), was dose dependent. Protein synthesis was not involved in the CD14 hyperexpression since it was not influenced by co-incubation with cycloheximide. Finally, LPS-induced up-regulation of monocyte CD14 was associated with an increased binding of fluoresceinated LPS. We conclude that LPS in whole blood up-regulates the expression of its own CD14 receptor on monocytes, a phenomenon that could be relevant to the pathogenesis of gram-negative sepsis.
我们通过流式细胞术检测了在人全血中加入脂多糖(LPS)后单核细胞上脂多糖受体CD14分子的表达。在30分钟内,LPS诱导单核细胞CD14表达增加,在1至3小时达到峰值,随后缓慢下降。抗CD14单克隆抗体结合位点的最大增加估计为基础值的两倍。这种效应在极低浓度的LPS(10 pg/ml)下就已观察到,且呈剂量依赖性。蛋白质合成不参与CD14的过度表达,因为它不受与放线菌酮共同孵育的影响。最后,LPS诱导的单核细胞CD14上调与荧光素标记的LPS结合增加有关。我们得出结论,全血中的LPS上调了单核细胞上其自身CD14受体的表达,这一现象可能与革兰氏阴性脓毒症的发病机制有关。