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Toll样受体在慢性淋巴细胞白血病细胞中的表达及功能

Expression and function of toll like receptors in chronic lymphocytic leukaemia cells.

作者信息

Muzio Marta, Scielzo Cristina, Bertilaccio Maria T S, Frenquelli Michela, Ghia Paolo, Caligaris-Cappio Federico

机构信息

Department of Oncology, Unit and Laboratory of Lymphoid Malignancies, Istituto Scientifico San Raffaele and Università Vita-Salute San Raffaele, Milano, Italy.

出版信息

Br J Haematol. 2009 Feb;144(4):507-16. doi: 10.1111/j.1365-2141.2008.07475.x. Epub 2008 Nov 19.

Abstract

Mature B-cells can recognize microbial antigens via B-cell-receptor (BCR) in a specific way and via Toll-like receptors (TLR) in a costimulatory manner. A wealth of information is gathering on the possible role of antigenic stimulation in the natural history of Chronic Lymphocytic Leukaemia (CLL). However little is known regarding the repertoire and function of TLR in CLL cells. The TLR family includes 10 different transmembrane proteins devoted to recognize specific pathogen-associated molecular patterns and to alarm immunocompetent cells to trigger an immune response. Here, we studied fresh leukaemic cells for the expression pattern of TLR1 to TLR10, NOD1, NOD2 and SIGIRR (also known as TIR8). CLL cells were found to express several pattern recognition receptors including TLR1, TLR2, TLR6, TLR10, NOD1 and NOD2. The specific TLR expressed by CLL cells were functional. Leukaemic cells, upon stimulation with TLR1/2/6 ligands, such as bacterial lipopeptides, activated the nuclear factor-kappaB signalling pathway, expressed CD86 and CD25 activation molecules, and were protected from spontaneous apoptosis. These findings further support the hypothesis that CLL cells resemble antigen-activated B-cells and suggest a potential role of TLR in modulating CLL cell response in the context of specific antigen recognition.

摘要

成熟B细胞能够通过B细胞受体(BCR)以特异性方式识别微生物抗原,并通过Toll样受体(TLR)以共刺激方式识别。关于抗原刺激在慢性淋巴细胞白血病(CLL)自然病程中的可能作用,正在积累大量信息。然而,对于CLL细胞中TLR的组成和功能知之甚少。TLR家族包括10种不同的跨膜蛋白,专门用于识别特定的病原体相关分子模式,并向免疫活性细胞发出警报以触发免疫反应。在此,我们研究了新鲜白血病细胞中TLR1至TLR10、NOD1、NOD2和SIGIRR(也称为TIR8)的表达模式。发现CLL细胞表达多种模式识别受体,包括TLR1、TLR2、TLR6、TLR10、NOD1和NOD2。CLL细胞表达的特定TLR具有功能。白血病细胞在用TLR1/2/6配体(如细菌脂肽)刺激后,激活核因子-κB信号通路,表达CD86和CD25激活分子,并免受自发凋亡。这些发现进一步支持了CLL细胞类似于抗原激活的B细胞这一假说,并提示TLR在特定抗原识别背景下调节CLL细胞反应中可能发挥的作用。

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