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白色念珠菌酵母细胞与小鼠腘淋巴结组织的结合是由巨噬细胞介导的。

Binding of Candida albicans yeast cells to mouse popliteal lymph node tissue is mediated by macrophages.

作者信息

Han Y, van Rooijen N, Cutler J E

机构信息

Department of Microbiology, Montana State University, Bozeman 59717.

出版信息

Infect Immun. 1993 Aug;61(8):3244-9. doi: 10.1128/iai.61.8.3244-3249.1993.

Abstract

We previously reported that Candida albicans yeast cells adhere to the macrophage-rich medullary and subcapsular sinus areas of mouse lymph node tissue. To determine whether the yeast cell-lymph node interaction is mediated by macrophages, the effect of specific elimination of macrophages on yeast cell binding was studied, and yeast cell adherence was correlated with the ingestion of India ink by lymph node cells. Macrophage elimination was done by use of liposome-containing dichloromethylene diphosphonate (L-Cl2MDP). Mice were injected in the hind footpads with the L-Cl2MDP preparation, popliteal lymph nodes were removed 5 days later, and yeast cell adherence was determined by an ex vivo binding assay. As controls, lymph nodes from mice that received footpad injections of either phosphate-buffered saline (PBS) alone or liposome-containing PBS were used. Use of macrophage- and neutrophil-specific monoclonal antibodies in tissue immunostaining showed that the L-Cl2MDP treatment eliminated macrophages but not neutrophils from the medullary and subcapsular sinus areas of the popliteal lymph nodes. A striking reduction of yeast cell adherence occurred with lymph nodes from L-Cl2MDP-treated mice compared with lymph nodes from control animals. The lymph node-yeast cell binding patterns of L-Cl2MDP-treated and control mice were the same regardless of mouse strain, sex, or T-cell competency. Results of India ink experiments, in which India ink was injected into footpads of mice and was rapidly taken up by popliteal lymph node macrophages, showed a strong correlation between yeast adherence and India ink staining of cells. In addition, the interaction of yeast cells with lymph node tissue from normal mice was not significantly affected by the addition of two extracellular matrix proteins, fibronectin and laminin, during the ex vivo adherence assay. These data indicate that medullary and subcapsular sinus lymph node macrophages express an adhesion system similar to that described for mouse splenic marginal zone macrophages.

摘要

我们之前报道过,白色念珠菌酵母细胞可黏附于小鼠淋巴结组织中富含巨噬细胞的髓质和被膜下窦区域。为了确定酵母细胞与淋巴结的相互作用是否由巨噬细胞介导,我们研究了特异性清除巨噬细胞对酵母细胞黏附的影响,并将酵母细胞黏附与淋巴结细胞摄取印度墨汁的情况相关联。通过使用含二氯亚甲基二膦酸盐的脂质体(L-Cl2MDP)来清除巨噬细胞。给小鼠后足垫注射L-Cl2MDP制剂,5天后取出腘窝淋巴结,通过体外结合试验测定酵母细胞黏附情况。作为对照,使用接受单独足垫注射磷酸盐缓冲盐水(PBS)或含脂质体PBS的小鼠的淋巴结。在组织免疫染色中使用巨噬细胞和中性粒细胞特异性单克隆抗体表明,L-Cl2MDP处理可从腘窝淋巴结的髓质和被膜下窦区域清除巨噬细胞,但不能清除中性粒细胞。与对照动物的淋巴结相比,L-Cl2MDP处理小鼠的淋巴结中酵母细胞黏附显著减少。无论小鼠品系、性别或T细胞功能如何,L-Cl2MDP处理和对照小鼠的淋巴结-酵母细胞结合模式均相同。印度墨汁实验结果显示,将印度墨汁注射到小鼠足垫中并被腘窝淋巴结巨噬细胞迅速摄取,酵母黏附与细胞的印度墨汁染色之间存在很强的相关性。此外,在体外黏附试验中添加两种细胞外基质蛋白纤连蛋白和层粘连蛋白,对酵母细胞与正常小鼠淋巴结组织的相互作用没有显著影响。这些数据表明,髓质和被膜下窦淋巴结巨噬细胞表达的黏附系统类似于小鼠脾边缘区巨噬细胞所描述的黏附系统。

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