Onori P, Franchitto A, Sferra R, Vetuschi A, Gaudio E
Department of Experimental Medicine, Human & Clinical Anatomy, State University of L'Aquila, Italy.
Dig Dis Sci. 2001 May;46(5):1095-104. doi: 10.1023/a:1010778532240.
The epithelial layer covering lymphoid follicles of Peyer's patches consists of cells with a different surface morphology. Some of these cells have been described as a distinct cytotype, the so-called M cells. In order to resolve the controversy on the specific morphological and biochemical markers of M cells, structural, ultrastructural, and morphometrical study of the epithelium covering the rat Peyer's patches were performed. Peyer's patches from healthy rats were processed for light microscopy, immunohistochemistry, in situ nick-end labeling (TUNEL), and scanning and transmission electron microscopy. A morphometric study was also performed to evaluate microvillus density, length, and number of lysosomes in different areas of the epithelium. Peyer's patches were covered by simple columnar/cubical dome epithelium (DE). Scarce goblet cells and a large number of enterocytes were observed. Ultrastructural observations revealed that the DE showed cells with different morphology. The density and length of microvilli and the lysosome number varied along the whole dome without significant differences. The DE cells characterized by short and disorganized microvilli appeared always in close spatial relationship with lymphocytes. In conclusion, the concept that distinct cell types (enterocytes and M cells) can be identified in the rat DE does not appear to be valid based on morphological criteria. It seems correct to consider that in rat Peyer's patches the presence of scarce goblet cells and a large number of enterocytes showing dynamic morphofunctional modifications is related to the functional state and/or to cell cycle.
覆盖派尔集合淋巴结淋巴滤泡的上皮层由具有不同表面形态的细胞组成。其中一些细胞被描述为一种独特的细胞类型,即所谓的M细胞。为了解决关于M细胞特定形态和生化标志物的争议,对覆盖大鼠派尔集合淋巴结的上皮进行了结构、超微结构和形态计量学研究。将来自健康大鼠的派尔集合淋巴结进行处理,用于光学显微镜检查、免疫组织化学、原位缺口末端标记(TUNEL)以及扫描和透射电子显微镜检查。还进行了形态计量学研究,以评估上皮不同区域的微绒毛密度、长度和溶酶体数量。派尔集合淋巴结被单层柱状/立方顶上皮(DE)覆盖。观察到少量杯状细胞和大量肠上皮细胞。超微结构观察显示,DE显示出具有不同形态的细胞。微绒毛的密度和长度以及溶酶体数量在整个顶部均有变化,但无显著差异。以短而紊乱的微绒毛为特征的DE细胞总是与淋巴细胞保持紧密的空间关系。总之,基于形态学标准,在大鼠DE中可识别出不同细胞类型(肠上皮细胞和M细胞)这一概念似乎并不成立。认为在大鼠派尔集合淋巴结中,少量杯状细胞和大量表现出动态形态功能改变的肠上皮细胞的存在与功能状态和/或细胞周期有关,这似乎是正确的。