Kelleher D, Murphy A, Lynch S, O'Farrelly C
Department of Clinical Medicine, Trinity College, Dublin, Ireland.
Eur J Immunol. 1994 Apr;24(4):1013-6. doi: 10.1002/eji.1830240437.
The expression of adhesion molecules by human duodenal intraepithelial lymphocytes (IEL) was examined by two-color flow cytometry. Resting IEL expressed LFA-1, HML-1, CD44. Stimulation with phytohemagglutinin (PHA) resulted in down-regulation of expression of these molecules with induction of expression of ICAM-1 and VLA-4. VLA-4 expression was also found on non-activated IEL from patients with celiac disease. In addition, IEL expressed an antigen recognized by a novel monoclonal antibody D2.1. The molecular mass of D2.1 is heterogeneous: 82 kDa in peripheral blood lymphocytes and 44 kDa in an IEL line. Expression of this antigen was also up-regulated by PHA. To determine the involvement of these antigens in binding of IEL to human enterocytes, we developed a system based on adherence of an IEL cell line to the I407 fetal intestinal cell line. Monoclonal antibodies VLA-4, D2.1 and to a lesser extent ICAM-1 blocked adherence of IEL to I407 cells. These data suggest that VLA-4 and D2.1 may be involved in adherence of IEL to human enterocytes or secreted matrix molecules in vivo.
采用双色流式细胞术检测人十二指肠上皮内淋巴细胞(IEL)黏附分子的表达。静息IEL表达淋巴细胞功能相关抗原-1(LFA-1)、人黏膜淋巴细胞抗原-1(HML-1)、淋巴细胞功能相关抗原-44(CD44)。用植物血凝素(PHA)刺激导致这些分子表达下调,并诱导细胞间黏附分子-1(ICAM-1)和极迟抗原-4(VLA-4)表达。在乳糜泻患者的未激活IEL上也发现了VLA-4表达。此外,IEL表达一种可被新型单克隆抗体D2.1识别的抗原。D2.1的分子量具有异质性:外周血淋巴细胞中为82 kDa,IEL系中为44 kDa。该抗原的表达也被PHA上调。为了确定这些抗原在IEL与人肠上皮细胞结合中的作用,我们建立了一个基于IEL细胞系与I407胎儿肠细胞系黏附的系统。单克隆抗体VLA-4、D2.1以及程度较轻的ICAM-1可阻断IEL与I407细胞的黏附。这些数据表明,VLA-4和D2.1可能参与IEL在体内与人肠上皮细胞或分泌的基质分子的黏附。