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树突状网状细胞的产后发育及其免疫复合物捕获能力。

Postnatal development of dendritic reticulum cells and their immune complex trapping ability.

作者信息

Imai Y, Dobashi M, Terashima K

机构信息

Department of Pathology, Yamagata University School of Medicine, Japan.

出版信息

Histol Histopathol. 1986 Jan;1(1):19-26.

PMID:2980099
Abstract

The postnatal development of dendritic reticulum cells in the rat popliteal lymph nodes was electron microscopically investigated in relation to the appearance of immune complex trapping capacity. The popliteal lymph nodes of neonatal rat consisted of loosely arranged fibroblastic reticulum cells. In the following stage, the peripheral cortex and paracortex became distinguishable. The former was made up of an accumulation of small lymphocytes, scattered within a framework of reticulum cells. On te 28 th day, the first primary follicle appeared in the peripheral cortex. Simultaneously the immune complex could be trapped on the cytoplasmic membrane of reticulum cells, which were located in the central portion of the primary follicles. The early image of germinal centers appeared corresponding to immune complex trapping areas. In the well-developed secondary follicles, the immune complex trapping cells were mainly localized in the cap area. Their cytoplasmic membranes formed the dendritic processes, on which the distinct ability of trapping of the immune complex was recognized. It was demonstrated that the fibroblastic reticulum cells, forming the stroma of lymph nodes, were transformed into the typical dendritic reticulum cells with labyrinth structures in the cap area. Desmosomal junctions were often found, not only between the dendritic reticulum cells themselves, but also between the dendritic reticulum cells and lymphocytes. We suggest that the desmosomal junctions play a role as the channel for a transmission of immunological information.

摘要

运用电子显微镜技术,研究了大鼠腘淋巴结中树突状网状细胞的产后发育及其与免疫复合物捕获能力出现的关系。新生大鼠的腘淋巴结由排列疏松的成纤维网状细胞组成。在随后的阶段,外周皮质和副皮质变得可区分。前者由聚集在网状细胞框架内的小淋巴细胞组成。在第28天,第一个初级滤泡出现在外周皮质。同时,免疫复合物可捕获在位于初级滤泡中心部分的网状细胞的细胞质膜上。生发中心的早期图像与免疫复合物捕获区域相对应。在发育良好的次级滤泡中,免疫复合物捕获细胞主要定位于帽区。它们的细胞质膜形成树突状突起,在其上可识别出明显的免疫复合物捕获能力。结果表明,构成淋巴结基质的成纤维网状细胞在帽区转化为具有迷宫结构的典型树突状网状细胞。不仅在树突状网状细胞自身之间,而且在树突状网状细胞与淋巴细胞之间,经常发现桥粒连接。我们认为桥粒连接作为免疫信息传递的通道发挥作用。

相似文献

1
Postnatal development of dendritic reticulum cells and their immune complex trapping ability.树突状网状细胞的产后发育及其免疫复合物捕获能力。
Histol Histopathol. 1986 Jan;1(1):19-26.
2
A change in the localization of the region trapping immune complexes in rat popliteal lymph nodes during development of germinal centers, with regard to the distribution of follicular dendritic cells.关于生发中心发育过程中大鼠腘淋巴结内捕获免疫复合物区域的定位变化与滤泡树突状细胞分布的关系。
Histol Histopathol. 1996 Apr;11(2):293-302.
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Transport of immune complexes from the subcapsular sinus to lymph node follicles on the surface of nonphagocytic cells, including cells with dendritic morphology.免疫复合物从被膜下窦运输至淋巴结滤泡,通过非吞噬细胞表面进行,包括具有树突状形态的细胞。
J Immunol. 1983 Oct;131(4):1714-27.
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The ultrastructure of the abdominal lymph nodes cortex in rats during primary and secondary immune response (a special reference to dendritic reticulum cells and interdigitating cells).大鼠初次和二次免疫反应期间腹部淋巴结皮质的超微结构(特别提及树突状网状细胞和交错突细胞)
Morphol Embryol (Bucur). 1990 Jan-Mar;36(1):49-58.
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A novel in vivo follicular dendritic cell-dependent iccosome-mediated mechanism for delivery of antigen to antigen-processing cells.一种新的体内滤泡树突状细胞依赖性免疫体介导的将抗原递呈给抗原处理细胞的机制。
J Immunol. 1988 Jan 15;140(2):341-53.
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Appearance of the reticular cells which trap antigens in the rat lymph node in postnatal development.大鼠淋巴结中捕获抗原的网状细胞在出生后发育过程中的外观。
J Electron Microsc (Tokyo). 1991 Dec;40(6):378-84.
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Ontogeny of the follicular dendritic cell phenotype and function in the postnatal murine spleen.出生后小鼠脾脏中滤泡树突状细胞表型和功能的个体发生
Cell Immunol. 2001 Nov 25;214(1):45-53. doi: 10.1006/cimm.2001.1874.
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Function of the follicular dendritic cell in the germinal center of lymphoid follicles.滤泡树突状细胞在淋巴滤泡生发中心的功能。
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[Effect of blockage of the afferent lymphatic vessels on the development of popliteal lymph nodes in the rat].[阻断传入淋巴管对大鼠腘淋巴结发育的影响]
Kaibogaku Zasshi. 1989 Dec;64(6):550-60.

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