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日粮胆碱缺乏和过量可能通过调节幼建鲤的NF-κB、STAT和p38 MAPK信号分子,诱导肠道炎症和肠道紧密连接蛋白转录的改变。

Dietary choline deficiency and excess induced intestinal inflammation and alteration of intestinal tight junction protein transcription potentially by modulating NF-κB, STAT and p38 MAPK signaling molecules in juvenile Jian carp.

作者信息

Wu Pei, Jiang Wei-Dan, Jiang Jun, Zhao Juan, Liu Yang, Zhang Yong-An, Zhou Xiao-Qiu, Feng Lin

机构信息

Animal Nutrition Institute, Sichuan Agricultural University, Chengdu, 611130, China; Fish Nutrition and Safety Production University Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, 611130, China; Key Laboratory for Animal Disease-Resistance Nutrition of China Ministry of Education, Sichuan Agricultural University, Chengdu, 611130, China.

Fish Nutrition and Safety Production University Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, 611130, China; Key Laboratory for Animal Disease-Resistance Nutrition of China Ministry of Education, Sichuan Agricultural University, Chengdu, 611130, China.

出版信息

Fish Shellfish Immunol. 2016 Nov;58:462-473. doi: 10.1016/j.fsi.2016.09.055. Epub 2016 Sep 28.

Abstract

This study investigated the effects of choline on intestinal mucosal immune and the possible mechanisms in fish by feeding juvenile Jian carp (Cyprinus carpio var. Jian) with graded levels of dietary choline (165-1820 mg/kg diet) for 65 days. The results firstly showed that choline deficiency induced inflammatory infiltration in the proximal intestine (PI), mid intestine (MI) and distal intestine (DI) of fish. Meanwhile, compared with the optimal choline group, choline deficiency decreased the activities of lysozyme and acid phosphatase, contents of complement 3 and IgM in the intestine, downregulated the mRNA levels of antimicrobial peptides (liver-expressed antimicrobial peptide (LEAP) 2A and defensin-3 in the PI and MI, LEAP-2B and hepcidin in the PI, MI and DI), anti-inflammatory cytokines (interleukin (IL) 10 and transforming growth factor β2 in the PI, MI and DI), and signaling molecule IκB in the PI, MI and DI; while upregulated the mRNA levels of pro-inflammatory cytokines (IL-6a and tumor necrosis factor α in the MI and DI, interferon γ2b in the PI and MI, IL-1β and IL-6b in the PI, MI and DI), and signaling molecules (Toll-like receptor 4 in the MI, myeloid differentiation primary response 88 in the PI and MI, Janus kinase 3 and tyrosine kinase 2 in the MI and DI, nuclear factor kappa B (NF-κB), signal transducers and activators of transcription (STAT) 4 and STAT5 in the PI, MI and DI) of juvenile Jian carp, further indicating that choline deficiency caused inflammation and immunity depression in the intestine of fish. But choline deficiency decreased the PI IL-6a mRNA level, and increased the DI LEAP-2A and defensin-3 mRNA levels with unknown reasons. Furthermore, dietary choline deficiency downregulated mRNA levels of tight junction (TJ) proteins (claudin 3c in the PI and MI, claudin 7, claudin 11 and occludin in the PI, MI and DI) and signaling molecule mitogen-activated protein kinases p38 in the PI, MI and DI of juvenile Jian carp, whereas upregulated the mRNA levels of claudin 3b in the MI and DI, and claudin 3c in the DI. Moreover, the excessive choline exhibited negative effects on intestinal immunity and TJ proteins that were similar to the choline deficiency. In summary, dietary choline deficiency or excess caused the depression of intestinal mucosal immune by inducing inflammation and dysfunction of the intestinal physical barrier, and regulating related signaling molecules of fish.

摘要

本研究通过给建鲤幼鱼投喂不同胆碱水平(165 - 1820毫克/千克饲料)的饲料65天,探究了胆碱对鱼类肠道黏膜免疫的影响及其可能机制。结果首先表明,胆碱缺乏诱导了鱼类近端肠道(PI)、中段肠道(MI)和远端肠道(DI)的炎症浸润。同时,与最佳胆碱组相比,胆碱缺乏降低了肠道中溶菌酶和酸性磷酸酶的活性、补体3和IgM的含量,下调了抗菌肽(PI和MI中的肝脏表达抗菌肽(LEAP)2A和防御素-3,PI、MI和DI中的LEAP-2B和铁调素)、抗炎细胞因子(PI、MI和DI中的白细胞介素(IL)10和转化生长因子β2)以及PI、MI和DI中信号分子IκB的mRNA水平;而上调了建鲤幼鱼促炎细胞因子(MI和DI中的IL-6a和肿瘤坏死因子α,PI和MI中的干扰素γ2b,PI、MI和DI中的IL-1β和IL-6b)以及信号分子(MI中的Toll样受体4,PI和MI中的髓样分化初级反应88,MI和DI中的Janus激酶3和酪氨酸激酶2,PI、MI和DI中的核因子κB(NF-κB)、信号转导和转录激活因子(STAT)4和STAT5)的mRNA水平,进一步表明胆碱缺乏导致鱼类肠道炎症和免疫抑制。但胆碱缺乏使PI中IL-6a mRNA水平降低,而DI中LEAP-2A和防御素-3 mRNA水平升高,原因不明。此外,饲料中胆碱缺乏下调了建鲤幼鱼PI、MI和DI中紧密连接(TJ)蛋白(PI和MI中的claudin 3c,PI、MI和DI中的claudin 7、claudin 11和闭合蛋白)以及信号分子丝裂原活化蛋白激酶p38的mRNA水平,而MI和DI中claudin 3b以及DI中claudin 3c的mRNA水平上调。此外,过量胆碱对肠道免疫和TJ蛋白也有负面影响,与胆碱缺乏类似。总之,饲料中胆碱缺乏或过量通过诱导炎症和肠道物理屏障功能障碍以及调节鱼类相关信号分子,导致肠道黏膜免疫抑制。

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