首页> 外文期刊>American Journal of Pathology >Differential Expression of Ca2+-Binding Proteins on Follicular Dendritic Cells in Non-Neoplastic and Neoplastic Lymphoid Follicles
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Differential Expression of Ca2+-Binding Proteins on Follicular Dendritic Cells in Non-Neoplastic and Neoplastic Lymphoid Follicles

机译:Ca2 +结合蛋白在非赘生性和赘生性淋巴滤泡的卵泡树突状细胞中的差异表达。

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摘要

We studied the Ca2+-capture ability of follicular dendritic cells (FDCs) in tonsillar secondary lymphoid follicles (LFs) and the expression of six Ca2+-binding proteins (CBPs), caldesmon, S-100 protein, calcineurin, calbindin-D, calmodulin, and annexin VI in LFs of various lymphoid tissues and caldesmon and S-100 protein in neoplastic follicles of follicular lymphomas. First, Ca2+-capture cytochemistry revealed extensive Ca2+ capture in the nuclei and cytoplasm of FDCs, but little or none in follicular lymphocytes. All six CBPs were localized immunohistochemically in the LFs and were always present in the basal light zone. Immunoelectron microscopic staining of FDCs was classified into two patterns: caldesmon was distributed in the peripheral cytoplasm like a be S-100 protein, calcineurin, calbindin-D, and calmodulin were distributed diffusely in the cytosol. Annexin VI was, however, negative on FDCs. Immunocytochemistry also demonstrated CBP-positive FDCs within FDC-associated clusters isolated from germinal centers. In situ hybridization revealed diffuse calmodulin mRNA expression throughout the secondary LFs. These data indicate that the CBPs examined may regulate Ca2+ in the different subcellular sites of FDCs, and the roles of CBPs may be heterogeneous. We also investigated the distribution of caldesmon and S-100 protein in follicular lymphomas on paraffin-embedded tissue sections. FDCs within grades I and II neoplastic follicles clearly expressed caldesmon, but not S-100 protein, except a part of grade II neoplastic follicles. FDCs within grade III follicles showed no caldesmon, but frequently expressed S-100 protein. These results demonstrate that the caldesmon and S-100 protein staining patterns of grade I follicular lymphomas are different from those of grade III follicular lymphomas and suggest that FDC networks in grade I neoplastic follicles may be similar to those in the light zone within non-neoplastic follicles, FDC networks in grade III neoplastic follicles may be similar to those in dark and basal light zones within non-neoplastic follicles, and grade II follicles may be intermediate between grade I and grade III follicles.
机译:我们研究了扁桃体继发性淋巴滤泡(LFs)中卵泡树突状细胞(sfc)的Ca 2 + 捕获能力以及 的六个表达Ca 2 + 结合蛋白(CBPs),caldesmon, S-100蛋白,钙调神经磷酸酶,calbindin-D,钙调蛋白和膜联蛋白 VI滤泡性淋巴瘤赘生性滤泡中各种淋巴组织和Caldesmon的LF和S-100蛋白 。首先,Ca 2 + -捕获 细胞化学揭示了FDC的核 和细胞质中广泛的Ca 2 + 捕获, 所有六个CBPs免疫组织化学定位在LFs 中,并且始终存在于基底轻区。 FDCs的免疫电子 显微染色分为两种模式: caldesmon分布在周围的细胞质中,像是 皮带。 S-100蛋白,钙调神经磷酸酶,钙结合蛋白D和钙调蛋白 分散地分布在细胞质中。但是,膜联蛋白VI在FDC上为 阴性。免疫细胞化学还显示了从生发中心分离的FDC相关簇中的CBP阳性 FDC。 原位杂交显示在整个次要LF中弥漫性钙调蛋白mRNA表达 。 。这些数据表明,所检查的CBPs可能在FDC的不同亚细胞部位 中调节Ca 2 + ,并且CBPs的作用可能是异质的。我们还 研究了石蜡包埋的组织切片上滤泡性淋巴瘤中的Caldesmon和S-100蛋白 的分布。卵泡清楚地表达了 Caldesmon,但没有表达S-100蛋白,只是II 肿瘤性卵泡的一部分。 III级卵泡内的FDCs显示没有 caldesmon,但经常表达S-100蛋白。这些 结果表明,I级滤泡性淋巴瘤的caldesmon和S-100蛋白染色 模式与III级滤泡性淋巴瘤的 模式不同,因此建议I级肿瘤滤泡中的FDC 网络可能与非肿瘤滤泡轻区中的 相似,III级肿瘤滤泡中的FDC网络 卵泡可能与非肿瘤性卵泡内的 暗区和基底亮区的卵泡相似, 和II级卵泡可能介于I级和 之间III级卵泡。

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    《American Journal of Pathology》 |1999年第3期|00000805-00000814|共10页
  • 作者单位

    From the Second Department of Internal Medicine,Yamagata University School of Medicine, Yamagata, Japan|and First Department of Pathology,Yamagata University School of Medicine, Yamagata, Japan;

    and First Department of Pathology,Yamagata University School of Medicine, Yamagata, Japan;

    From the Second Department of Internal Medicine,Yamagata University School of Medicine, Yamagata, Japan;

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  • 入库时间 2022-08-17 14:17:21

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