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产生单核因子的细胞在非肥胖糖尿病(NOD)胰岛炎的募集阶段占主导地位,而产生Th1型细胞因子的细胞则是效应阶段的特征。

Monokine-producing cells predominate in the recruitment phase of NOD insulitis while cells producing Th1-type cytokines characterize the effector phase.

作者信息

Pilström B, Björk L, Böhme J

机构信息

Department of Immunology, The Wenner-Gren Institute, Stockholm University, Sweden.

出版信息

J Autoimmun. 1997 Apr;10(2):147-55. doi: 10.1006/jaut.1996.0115.

Abstract

Cells infiltrating the Langerhans' islets of prediabetic NOD females were isolated from 6 weeks to 6 months of age. These cells were assayed at a single-cell level for production of eight different cytokines by intracellular immunofluorescent staining. Quiescent in vivo preactivated cells were detected by in vitro stimulation with PMA and ionomycin for 4 h. The cell recruitment phase, between 6 and 12 weeks of age, is predominated by production of the monokines IL-1alpha, IL-6, and TNF After stimulation IFN-gamma and occasional IL-10 and GM-CSF producing cells could also be observed. This cytokine pattern occurs simultaneously with increasing insulitis, and we suggest that these cytokines are important in attracting inflammatory cells to the islets and maintaining the inflammatory state. A high frequency of endocrine cells producing IL-6 during this period may denote a stress response caused by initial beta-cell destruction due to cytokines released by the inflammatory cells. During the effector phase, between 4 and 6 months, there is a characteristic Th1 cytokine profile with lymphocytes producing IL-2, IFN-gamma and TNF, supposedly TNF-beta. No IL-4 production could be detected and IL-10 was very rarely found, indicating the absence of a Th2 response. Our findings show that the effector phase in NOD insulitis is a Th1 rather than a Th2-mediated event. We also demonstrate that cytokines that may cause initial tissue destruction are produced during the recruitment of inflammatory cells.

摘要

从6周龄至6月龄的糖尿病前期非肥胖糖尿病(NOD)雌性小鼠的胰岛中分离出浸润细胞。通过细胞内免疫荧光染色在单细胞水平上检测这些细胞产生的八种不同细胞因子。通过用佛波酯(PMA)和离子霉素体外刺激4小时来检测体内静止的预激活细胞。在6至12周龄的细胞募集阶段,主要产生单核因子白细胞介素-1α(IL-1α)、白细胞介素-6(IL-6)和肿瘤坏死因子(TNF)。刺激后,还可观察到产生干扰素-γ(IFN-γ)以及偶尔产生白细胞介素-10(IL-10)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)的细胞。这种细胞因子模式与胰岛炎的加重同时出现,我们认为这些细胞因子在吸引炎症细胞到胰岛并维持炎症状态方面很重要。在此期间产生IL-6的内分泌细胞的高频率可能表示由炎症细胞释放的细胞因子导致的初始β细胞破坏引起的应激反应。在4至6个月的效应阶段,有一个特征性的Th1细胞因子谱,淋巴细胞产生白细胞介素-2(IL-2)、干扰素-γ和肿瘤坏死因子,推测为肿瘤坏死因子-β(TNF-β)。未检测到白细胞介素-4(IL-4)的产生,并且很少发现白细胞介素-10,表明不存在Th2反应。我们的研究结果表明,NOD胰岛炎的效应阶段是由Th1而非Th2介导的事件。我们还证明,在炎症细胞募集期间会产生可能导致初始组织破坏的细胞因子。

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