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次级淋巴器官正常微结构所需的p52/NF-κB的不同活性:由Bcl-3增强的功能

Distinct activities of p52/NF-kappa B required for proper secondary lymphoid organ microarchitecture: functions enhanced by Bcl-3.

作者信息

Poljak L, Carlson L, Cunningham K, Kosco-Vilbois M H, Siebenlist U

机构信息

Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA.

出版信息

J Immunol. 1999 Dec 15;163(12):6581-8.

Abstract

Mice rendered deficient in p52, a subunit of NF-kappa B, or in Bcl-3, an I kappa B-related regulator that associates with p52 homodimers, share defects in the microarchitecture of secondary lymphoid organs. The mutant mice are impaired in formation of B cell follicles and are unable to form proper follicular dendritic cell (FDC) networks upon antigenic challenge. The defects in formation of B cell follicles may be attributed, at least in part, to impaired production of the B lymphocyte chemoattractant (BLC) chemokine, possibly a result of defective FDCs. The p52- and Bcl-3-deficient mice exhibit additional defects within the splenic marginal zone, including reduced numbers of metallophilic macrophages, reduced deposition of the laminin-beta 2 chain and impaired expression of a mucosal addressin marker on sinus-lining cells. Whereas p52-deficient mice are severely defective in all of these aspects, Bcl-3-deficient mice are only partially defective. We determined that FDCs or other non-hemopoietic cells that underlie FDCs are intrinsically impaired in p52-deficient mice. Adoptive transfers of wild-type bone marrow into p52-deficient mice failed to restore FDC networks or follicles. The transfers did restore metallophilic macrophages to the marginal zone, however. Together, the results suggest that p52 carries out functions essential for a proper splenic microarchitecture in both hemopoietic and non-hemopoietic cells and that Bcl-3 is important in enhancing these essential activities of p52.

摘要

p52(核因子-κB的一个亚基)或Bcl-3(一种与p52同二聚体相关的IκB相关调节因子)功能缺失的小鼠,在二级淋巴器官的微观结构上存在共同缺陷。这些突变小鼠在B细胞滤泡形成方面受损,并且在抗原刺激后无法形成正常的滤泡树突状细胞(FDC)网络。B细胞滤泡形成的缺陷可能至少部分归因于B淋巴细胞趋化因子(BLC)趋化因子产生受损,这可能是FDC缺陷的结果。p52和Bcl-3缺陷的小鼠在脾边缘区还表现出其他缺陷,包括嗜金属巨噬细胞数量减少、层粘连蛋白-β2链沉积减少以及窦衬细胞上黏膜地址素标志物的表达受损。虽然p52缺陷的小鼠在所有这些方面都存在严重缺陷,但Bcl-3缺陷的小鼠只是部分缺陷。我们确定,在p52缺陷的小鼠中,FDC或构成FDC的其他非造血细胞存在内在缺陷。将野生型骨髓过继转移到p52缺陷的小鼠中未能恢复FDC网络或滤泡。然而,这种转移确实使嗜金属巨噬细胞恢复到了边缘区。总之,这些结果表明,p52在造血细胞和非造血细胞中都执行着对适当脾微观结构至关重要的功能,并且Bcl-3在增强p52的这些基本活性方面很重要。

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