Karseladze A I
Department of Morphological and Molecular Genetic Tumor Diagnostics, N. N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow, Russia.
Department of Oncopathology, V. I. Kulakov National Medical Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of the Russian Federation, Moscow, Russia.
Bull Exp Biol Med. 2023 Feb;174(4):502-508. doi: 10.1007/s10517-023-05737-x. Epub 2023 Mar 10.
We studied the features of reaction of the colon stromal cells (lymphohistiocytic population, fibroblasts, and blood vessels) to the appearance and progression of dysplasia in the colon epithelium against the background of increasing ischemia in the colon mucosa. The morphological material from 92 patients treated for benign processes and colon cancer in 2002-2016 was examined. Common histological methods and a complex immunohistochemical staining were used. The stromal cells of the colon mucosa, mainly lymphohistiocytic cells, undergo certain quantitative changes specific for each type of cells during progression of dysplasia and aggravation of ischemia in the mucosa. Some cells, e.g. plasma cells, presumably contribute to tissue hypoxia in the stroma. Most stromal cells, except interdigitating S100 dendritic cells and CD10 fibroblasts, decreased at the stage of grave dysplasia and cancer in situ. Low effectiveness of the immune defense can be partly explained by impairment of the function of stromal cells as a result of hypoxia in the microenvironment.
我们研究了在结肠黏膜缺血加重的背景下,结肠基质细胞(淋巴细胞组织细胞群体、成纤维细胞和血管)对结肠上皮发育异常的出现和进展的反应特征。检查了2002年至2016年因良性病变和结肠癌接受治疗的92例患者的形态学资料。采用常规组织学方法和复合免疫组织化学染色。在发育异常进展和黏膜缺血加重过程中,结肠黏膜的基质细胞,主要是淋巴细胞组织细胞,会经历特定于每种细胞类型的某些定量变化。一些细胞,如浆细胞,可能导致基质中的组织缺氧。除了交错的S100树突状细胞和CD10成纤维细胞外,大多数基质细胞在重度发育异常和原位癌阶段减少。免疫防御效率低下部分可归因于微环境缺氧导致基质细胞功能受损。