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新型禽腔上囊寡肽 BP9 对抗体反应、未成熟 B 细胞和自噬的作用和机制。

The Functions and Mechanism of a New Oligopeptide BP9 from Avian Bursa on Antibody Responses, Immature B Cell, and Autophagy.

机构信息

Key Laboratory of Animal Microbiology of China's Ministry of Agriculture, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.

Hospital of Nanjing Agricultural University, Nanjing 210095, China.

出版信息

J Immunol Res. 2019 Jan 6;2019:1574383. doi: 10.1155/2019/1574383. eCollection 2019.

Abstract

The bursa of Fabricius is an acknowledged central humoral immune organ unique to birds, which is vital to B cell differentiation and antibody production. However, the function and mechanism of the biological active peptide isolated from bursa on B cell development and autophagy were less reported. In this study, we isolated a new oligopeptide with nine amino acids Leu-Met-Thr-Phe-Arg-Asn-Glu-Gly-Thr from avian bursa following RP-HPLC, MODIL-TOP-MS, and MS/MS, which was named after BP9. The results of immunization experiments showed that mice injected with 0.01 and 0.05 mg/mL BP9 plus JEV vaccine generated the significant increased antibody levels, compared to those injected with JEV vaccine only. The microarray analysis on the molecular basis of BP9-treated immature B cell showed that vast genes were involved in various immune-related biological processes in BP9-treated WEHI-231 cells, among which the regulation of cytokine production and T cell activation were both major immune-related processes in WEHI-231 cells with BP9 treatment following network analysis. Also, the differentially regulated genes were found to be involved in four significantly enriched pathways in BP9-treated WEHI-231 cells. Finally, we proved that BP9 induced the autophagy formation, regulated the gene and protein expressions related to autophagy in immature B cell, and stimulated AMPK-ULK1 phosphorylation expression. These results suggested that BP9 might be a strong bursal-derived active peptide on antibody response, B cell differentiation, and autophagy in immature B cells, which provided the linking among humoral immunity, B cell differentiation, and autophagy and offered the important reference for the effective immunotherapeutic strategies and immune improvement.

摘要

法氏囊是一种公认的鸟类特有的中枢体液免疫器官,对 B 细胞分化和抗体产生至关重要。然而,从法氏囊中分离得到的具有生物活性的肽对 B 细胞发育和自噬的功能和机制的报道较少。在本研究中,我们采用 RP-HPLC、MODIL-TOP-MS 和 MS/MS 从禽类法氏囊中分离得到一种新的九肽,命名为 BP9,其氨基酸序列为 Leu-Met-Thr-Phe-Arg-Asn-Glu-Gly-Thr。免疫实验结果表明,与单独注射 JEV 疫苗的小鼠相比,注射 0.01 和 0.05mg/mL BP9 加 JEV 疫苗的小鼠产生了显著增加的抗体水平。BP9 处理未成熟 B 细胞的分子基础的微阵列分析表明,大量基因参与了 BP9 处理的 WEHI-231 细胞中的各种免疫相关的生物过程,其中,在网络分析后,BP9 处理 WEHI-231 细胞中细胞因子产生和 T 细胞激活的调节是主要的免疫相关过程。此外,差异调节基因被发现参与了 BP9 处理的 WEHI-231 细胞中四个显著富集的途径。最后,我们证明 BP9 诱导了自噬的形成,调节了未成熟 B 细胞中与自噬相关的基因和蛋白的表达,并刺激了 AMPK-ULK1 磷酸化的表达。这些结果表明,BP9 可能是一种强大的法氏囊来源的活性肽,对未成熟 B 细胞的抗体反应、B 细胞分化和自噬具有调节作用,为体液免疫、B 细胞分化和自噬之间的联系提供了重要参考,为有效的免疫治疗策略和免疫改善提供了重要参考。

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