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原发性干燥综合征中的核BCL10

Nuclear BCL10 in primary Sjögren's syndrome.

作者信息

Gatumu Margaret K, Jonsson Malin V, Øijordsbakken Gunnvor, Skarstein Kathrine

机构信息

Section for Pathology, The Gade Institute, University of Bergen, Bergen, Norway.

出版信息

J Oral Pathol Med. 2009 Jul;38(6):501-7. doi: 10.1111/j.1600-0714.2009.00757.x. Epub 2009 Mar 9.

Abstract

BACKGROUND

The events following triggering of antigen receptors and subsequent activation of the transcription factor nuclear factor kappa B (NFkappaB) need to be carefully controlled to prevent abnormal immune responses. BCL10 links the antigen receptor to NFkappaB. The aim of this study was to determine the expression pattern of BCL10 and NFkappaB in minor salivary gland infiltrates of patients with primary Sjögren's syndrome (pSS).

METHODS

Minor salivary glands from patients with primary SS (n = 17) and sicca controls (n = 4) were evaluated by single and double immunohistochemistry and immunofluorescence for confocal microscopy. BCL10 and NFkappaB-p65 expression were evaluated in the infiltrating lymphocytes. Ectopic germinal centers (GCs) were investigated by CD21. Tonsil, lymph node and lymphoma tissue were used as positive controls.

RESULTS

BCL10 nuclear positive cells were observed in focal lymphocytic infiltrates in the investigated minor salivary glands and were not restricted to patients with ectopic GCs. By double-staining, some of the BCL10 nuclear positive cells were identified as B cells. There was, however, no constitutive activation of NFkappaB as depicted by the exclusive cytoplasmic expression of p65 in the infiltrating lymphocytes in the pSS.

CONCLUSION

Nuclear expression of BCL10 in infiltrating lymphocytes was a common occurrence in pSS minor salivary glands indicating it as a possible marker of autoimmune induced chronic inflammation. There was, however, no constitutive activation of NFkappaB.

摘要

背景

抗原受体触发及随后转录因子核因子κB(NFκB)激活后的一系列事件需严格调控,以防止异常免疫反应。BCL10将抗原受体与NFκB连接起来。本研究旨在确定原发性干燥综合征(pSS)患者小唾液腺浸润中BCL10和NFκB的表达模式。

方法

采用单免疫组化、双免疫组化及免疫荧光共聚焦显微镜技术,对原发性干燥综合征患者(n = 17)和干燥对照组(n = 4)的小唾液腺进行评估。评估浸润淋巴细胞中BCL10和NFκB-p65的表达。通过CD21检测异位生发中心(GCs)。扁桃体、淋巴结及淋巴瘤组织用作阳性对照。

结果

在所研究的小唾液腺局灶性淋巴细胞浸润中观察到BCL10核阳性细胞,且不限于有异位GCs的患者。通过双重染色,部分BCL10核阳性细胞被鉴定为B细胞。然而,pSS浸润淋巴细胞中p65仅在细胞质表达,表明不存在NFκB的组成性激活。

结论

浸润淋巴细胞中BCL10的核表达在pSS小唾液腺中常见,提示其可能是自身免疫诱导的慢性炎症的一个标志物。然而,不存在NFκB的组成性激活。

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