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小鼠胰岛的体内显微镜检查:在器官特异性胰岛炎模型中,转移淋巴细胞与胰岛的粘附增加依赖于巨噬细胞衍生的细胞因子。

In vivo microscopy of murine islets of Langerhans: increased adhesion of transferred lymphocytes to islets depends on macrophage-derived cytokines in a model of organ-specific insulitis.

作者信息

Ludwig R, Kretschmer M, Caspar G, Bojunga J, Oldenburg A, Schumm-Draeger P, Stegmüller M, von Minckwitz G, Usadel K H, Kusterer K

机构信息

Department of Medicine I, J.W. Goethe University, Frankfurt am Main, Germany.

出版信息

Immunology. 1999 Sep;98(1):111-5. doi: 10.1046/j.1365-2567.1999.00826.x.

Abstract

Environmental factors contribute to the pathogenesis of type 1 diabetes (insulin-dependent diabetes mellitus). Multiple low doses of streptozotocin (MLDS) induce hyperglycaemia and insulitis in mice. Previously we demonstrated that adhesion of lymphocytes to endothelium of islets is only increased when donor animals were diabetic and recipient mice had received 5 mg/kg streptozotocin (STZ). Therefore we used streptozotocin to evaluate the immunological relevance of such an irritation of islets. Lymphocytes, separated from diabetic mice (MLDS), were fluorescently labelled and injected to recipient mice that had received 5 mg/kg STZ. With in vivo microscopy we measured lymphocyte flow and adherence in islets. Expression of vascular cell adhesion molecule-1 (VCAM-1) and intracellular adhesion molecule-1 (ICAM-1) in the pancreas was assessed using immunohistochemistry. Very late antigen-4 (VLA-4) and leucocyte function-associated antigen-1 (LFA-1) expression on transferred lymphocytes was measured with flow cytometry. Pretreatment of recipients with antibodies to cytokines or silica reduced lymphocyte adherence to islet endothelium from 2.04% (goat immunoglobulin G; IgG) or 1.82% (rat IgG) to 0.47, 0.58, 0.39 or 0. 19% for monoclonal antibody (mAb) interferon-gamma (IFN-gamma), polyclonal antibody (pAb) tumour necrosis factor-alpha (TNF-alpha), pAb interleukin (IL)-1alpha or silica, respectively. Reduced adhesion was associated with a decreased expression of VCAM-1 and ICAM-1 in islets of treated recipients compared with mice treated with 5 mg/kg STZ alone. In conclusion, pretreatment of recipients with 5 mg/kg STZ leads to an increased expression of adhesion molecules in the islets and lymphocyte adhesion to islet endothelium in vivo, demonstrating an immune response of the islets. Prevention of increased expression of ICAM-1 or VCAM-1 and reduction of lymphocyte adhesion in islets by silica or antibody indicate an involvement of macrophages and macrophage derived cytokines in the generation of this immune response.

摘要

环境因素在1型糖尿病(胰岛素依赖型糖尿病)的发病机制中起作用。多次低剂量链脲佐菌素(MLDS)可诱导小鼠出现高血糖和胰岛炎。此前我们证明,只有当供体动物患有糖尿病且受体小鼠接受了5mg/kg链脲佐菌素(STZ)时,淋巴细胞与胰岛内皮的黏附才会增加。因此,我们使用链脲佐菌素评估这种胰岛刺激的免疫相关性。从糖尿病小鼠(MLDS)中分离出淋巴细胞,进行荧光标记后注射到接受了5mg/kg STZ的受体小鼠体内。通过体内显微镜观察,我们测量了淋巴细胞在胰岛中的流动和黏附情况。使用免疫组织化学方法评估胰腺中血管细胞黏附分子-1(VCAM-1)和细胞间黏附分子-1(ICAM-1)的表达。用流式细胞术测量转移淋巴细胞上极迟抗原-4(VLA-4)和白细胞功能相关抗原-1(LFA-1)的表达。用细胞因子抗体或二氧化硅预处理受体,可使淋巴细胞与胰岛内皮的黏附从2.04%(山羊免疫球蛋白G;IgG)或1.82%(大鼠IgG)分别降至单克隆抗体(mAb)干扰素-γ(IFN-γ)、多克隆抗体(pAb)肿瘤坏死因子-α(TNF-α)、pAb白细胞介素(IL)-1α或二氧化硅处理后的0.47%、0.58%、0.39%或0.19%。与仅接受5mg/kg STZ处理的小鼠相比,处理后的受体小鼠胰岛中VCAM-1和ICAM-1表达降低,黏附减少与之相关。总之,用5mg/kg STZ预处理受体可导致体内胰岛中黏附分子表达增加以及淋巴细胞与胰岛内皮的黏附增加,表明胰岛存在免疫反应。二氧化硅或抗体可防止ICAM-1或VCAM-1表达增加并减少淋巴细胞在胰岛中的黏附,这表明巨噬细胞和巨噬细胞衍生的细胞因子参与了这种免疫反应的产生。

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Macrophage and lymphocyte homing in experimental diabetes.实验性糖尿病中巨噬细胞和淋巴细胞的归巢
Exp Clin Endocrinol Diabetes. 1999;107 Suppl 3:S102-7. doi: 10.1055/s-0029-1212162.

本文引用的文献

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Insulin-dependent diabetes mellitus.胰岛素依赖型糖尿病
Cell. 1996 May 3;85(3):291-7. doi: 10.1016/s0092-8674(00)81106-x.

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