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首页> 外文期刊>Veterinary research >The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells
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The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells

机译:新的法氏囊七肽(BP7)在免疫应答和未成熟B细胞中的免疫调节功能和分子机制

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摘要

The bursa of Fabricius (BF) is the acknowledged central humoural immune organ unique to birds and plays a vital role in B lymphocyte development. In addition, the unique molecular immune features of bursal-derived biological peptides involved in B cell development are rarely reported. In this paper, a novel bursal heptapeptide (BP7) with the sequence GGCDGAA was isolated from the BF and was shown to enhance the monoclonal antibody production of a hybridoma. A mouse immunization experiment showed that mice immunized with an AIV antigen and BP7 produced strong antibody responses and cell-mediated immune responses. Additionally, BP7 stimulated increased mRNA levels of sIgM in immature mouse WEHI-231 B cells. Gene microarray results confirmed that BP7 regulated 2465 differentially expressed genes in BP7-treated WEHI-231 cells and induced 13 signalling pathways and various immune-related functional processes. Furthermore, we found that BP7 stimulated WEHI-231 cell autophagy and AMPK-ULK1 phosphorylation and regulated Bcl-2 protein expression. Finally, chicken immunization showed that BP7 enhanced the potential antibody and cytokine responses to the AIV antigen. These results suggested that BP7 might be an active biological factor that functions as a potential immunopotentiator, which provided some novel insights into the molecular mechanisms of the effects of bursal peptides on immune functions and B cell differentiation.
机译:Fabricius(BF)的滑囊是公认的鸟类独特的中央体液免疫器官,在B淋巴细胞的发育中起着至关重要的作用。另外,很少报道涉及B细胞发育的囊性生物肽的独特分子免疫特征。在本文中,从BF中分离出了具有序列GCGCGAA的新型法氏囊七肽(BP7),并显示出它可以增强杂交瘤的单克隆抗体产生。小鼠免疫实验表明,用AIV抗原和BP7免疫的小鼠产生强抗体反应和细胞介导的免疫反应。此外,BP7刺激未成熟的小鼠WEHI-231 B细胞中sIgM的mRNA水平升高。基因芯片结果证实,BP7调节了BP7处理的WEHI-231细胞中2465个差异表达的基因,并诱导了13条信号通路和各种免疫相关功能过程。此外,我们发现BP7刺激WEHI-231细胞自噬和AMPK-ULK1磷酸化并调节Bcl-2蛋白表达。最后,鸡免疫显示BP7增强了对AIV抗原的潜在抗体和细胞因子应答。这些结果表明,BP7可能是一种潜在的免疫增强剂,可能是一个活跃的生物因子,这提供了法医肽对免疫功能和B细胞分化的分子机制的一些新见解。

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