Regoli M, Borghesi C, Bertelli E, Nicoletti C
Institute of Human Anatomy, University of Siena, Italy.
Ann Anat. 1995 Mar;177(2):119-24. doi: 10.1016/S0940-9602(11)80057-9.
The epithelium associated with the lymphoid follicles of Peyer's patches differs from the villi epithelium by the presence of M cells. The main function of these cells is to take up antigens (inert material, viruses and bacteria) from the intestinal lumen. The M cells are able to internalize various different gram-negative bacteria. In order to show the M cells ability to interact and take up a gram-positive bacterium, we exposed rabbit Peyer's patches to Streptococcus pneumoniae R36a. Using the isolated ileal loop technique, Peyer's patches were incubated with a bacterial suspension for varying periods (15, 30, 60, 100 minutes). The bacteria were found outside and inside the M cells. The internalized streptococci could be found in the M cell cytoplasm, in the cytoplasmic "pockets" and inside the intraepithelial lymphoid cells. The finding of internalized bacteria with their damaged walls suggests the possibility that M cells are able to modify internalized antigens in the same way as the antigen presenting cells.
与派尔集合淋巴结淋巴滤泡相关的上皮细胞因存在M细胞而与绒毛上皮不同。这些细胞的主要功能是从肠腔摄取抗原(惰性物质、病毒和细菌)。M细胞能够内化各种不同的革兰氏阴性菌。为了展示M细胞与革兰氏阳性菌相互作用并摄取的能力,我们将兔派尔集合淋巴结暴露于肺炎链球菌R36a。采用分离的回肠袢技术,将派尔集合淋巴结与细菌悬液孵育不同时间(15、30、60、100分钟)。在M细胞内外均发现了细菌。内化的链球菌可见于M细胞胞质、胞质“小窝”以及上皮内淋巴细胞内。发现内化细菌的细胞壁受损,提示M细胞有可能像抗原呈递细胞一样能够修饰内化抗原。