[免疫复合物病理条件下小鼠胸腺细胞死亡和淋巴结的基因毒性应激途径]。

N G Grushka, S I Pavlovych, T M Bryzgina, V S Sukhina, N V Makogon, R I Yanchiy
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引用次数: 2

摘要

采用牛血清白蛋白对CBA小鼠免疫系统损伤模型进行了基因毒性应激和免疫功能细胞死亡(凋亡和坏死)方式的研究。建立免疫小鼠的免疫荧光研究,免疫复合物在肝组织、脾、肾和主动脉的固定。这些器官的组织学研究显示血管系统的影响,在较小程度上,实质。经BSA免疫后,淋巴结细胞的DNA彗星指数增加了1.4倍,胸腺细胞的DNA彗星指数增加了1.5倍。我们还观察到胸腺(3.4倍)和淋巴结(3.3倍)DNA损伤最大的细胞数量分别增加,表明强烈的基因毒性应激。细胞活细胞数减少,死亡增加,包括促炎坏死和免疫原性坏死。由此,在实验模型上获得的数据证明,广义免疫复合物病理过程导致免疫系统中枢和外周器官的DNA损伤和ICC死亡。ICC基因毒性应激及其通过坏死方式的死亡扩增可能在免疫复合物疾病的发展中起重要作用。这些外周血淋巴细胞因子可作为评估自身免疫和免疫复合物疾病严重程度及其治疗效果的前瞻性检测系统。
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[Genotoxic stress and the pathways of thymus cell death and lymph nodes of mice in conditions of immunocomplex pathology].

There were performed the studies of genotoxic stress and the ways of immunocompetent cells death (apoptosis and necrosis) in the modeling of immune system damage by immunization of CBA mice with the bovine serum albumin. Immunofluorescence studies of immunized mice were established the fixation of immune complexes in liver tissue, spleen, kidney and the aorta. Histological studies of these organs showed vascular system affection and, to a lesser extent, parenchyma. It has been shown that DNA comets index increases in 1,4 time in the lymph node cells and in 1,5 time in the thymus cells in the presence of BSA immunization. We also observed an increase in the number of cells with maximum damage DNA thymus preparations (3.4 fold) and lymph nodes (3.3-fold), respectively, indicating strong genotoxic stress. There were shown the reduce of live ICC number and their death increase, including the pro-inflammatory and immunogenic necrotic way. In that way, data which were obtained on the experimental model is evidenced that generalized immunecomplex pathologic process leads to DNA damage and ICC death both central and peripheral organs of the immune system. ICC genotoxic stress and their death amplification by the necrotic way may play a significant role in the immunecomplex deseases development. These factors of peripheral blood lymphocytes can serve as a prospective test system for assessing the severity of autoimmune and immune complex diseases and their treatment effectiveness.

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