Bjerke K, Halstensen T S, Jahnsen F, Pulford K, Brandtzaeg P
Laboratory for Immunohistochemistry and Immunopathology (LIIPAT), University of Oslo, National Hospital, Rikshospitalet, Norway.
Gut. 1993 Oct;34(10):1357-63. doi: 10.1136/gut.34.10.1357.
Antibodies to the cytosolic leucocyte L1 protein (or calprotectin) were examined for reactivity with macrophages, neutrophils, and eosinophils identified by paired immunofluorescence staining in sections of normal human ileal mucosa, including Peyer's patches. Macrophages were recognised by expression of the myelomonocytic antigen CD68 (monoclonal antibody KP1). Neutrophilic granulocytes were identified by their content of neutrophil elastase, and eosinophilic granulocytes by monoclonal antibody EG2. Virtually all CD68+ macrophages in normal lamina propria and Peyer's patches were L1- and the same was true for most extravasated macrophages in normal peripheral lymph nodes. Some mesenteric lymph nodes, however, and all peripheral lymph nodes with overt pathological processes (malignant lymphoma) contained many CD68+L1+ macrophages. Numerous L1+ cells were also localised to the crypt region and to some extent beneath the villous epithelium in normal lamina propria, but they were mainly identified as EG2+ eosinophils. Such cells were remarkably scarce or absent beneath the follicle associated epithelium in the dome region of Peyer's patches, where CD68+L1- macrophages were abundant. Also subepithelial and interfollicular CD68- interdigitating dendritic cells in Peyer's patches (recognised by antibody to S-100 protein) were usually unreactive with L1 antibody. The L1 protein shows a broad spectrum of antimicrobial activities in vitro, and its putative antiproliferative properties are interesting in relation to the immunosuppression postulated to take place in lamina propria. The virtual absence of L1 producing cells beneath the follicle associated epithelium in Peyer's patches may support the immunostimulatory function of these macrophage rich structures, which are held to be crucial for induction of specific mucosal immunity.
通过对正常人回肠黏膜切片(包括派尔集合淋巴结)进行配对免疫荧光染色,检测细胞溶质白细胞L1蛋白(或钙卫蛋白)抗体与巨噬细胞、中性粒细胞和嗜酸性粒细胞的反应性。巨噬细胞通过髓单核细胞抗原CD68(单克隆抗体KP1)的表达来识别。中性粒细胞通过其所含的中性粒细胞弹性蛋白酶来鉴定,嗜酸性粒细胞则通过单克隆抗体EG2来鉴定。正常固有层和派尔集合淋巴结中几乎所有CD68+巨噬细胞均为L1阴性,正常外周淋巴结中大多数渗出的巨噬细胞也是如此。然而,一些肠系膜淋巴结以及所有有明显病理过程(恶性淋巴瘤)的外周淋巴结含有许多CD68+L1+巨噬细胞。在正常固有层的隐窝区域以及绒毛上皮下方也有许多L1+细胞,且在一定程度上存在,但它们主要被鉴定为EG2+嗜酸性粒细胞。在派尔集合淋巴结圆顶区域的滤泡相关上皮下方,此类细胞明显稀少或不存在,而该区域CD68+L1-巨噬细胞丰富。派尔集合淋巴结中的上皮下和滤泡间CD68-交错突细胞(通过抗S-100蛋白抗体识别)通常与L1抗体无反应。L1蛋白在体外显示出广泛的抗菌活性,其假定的抗增殖特性与固有层中假定发生的免疫抑制有关。派尔集合淋巴结滤泡相关上皮下方几乎不存在产生L1的细胞,这可能支持这些富含巨噬细胞的结构的免疫刺激功能,这些结构被认为对诱导特异性黏膜免疫至关重要。