• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

口服 LPS 给药可诱导小鼠胰腺淋巴结局部免疫变化。

Oral LPS Dosing Induces Local Immunological Changes in the Pancreatic Lymph Nodes in Mice.

机构信息

Department of Veterinary and Animal Sciences, University of Copenhagen, Grønnegårdsvej 15, 1870 Frederiksberg C, Denmark.

Department of Food Science, University of Copenhagen, Rolighedsvej 26, 1958 Frederiksberg C, Denmark.

出版信息

J Diabetes Res. 2019 Mar 6;2019:1649279. doi: 10.1155/2019/1649279. eCollection 2019.

DOI:10.1155/2019/1649279
PMID:30956991
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6431374/
Abstract

Lacking the initial contact between the immune system and microbial-associated molecular patterns (MAMPs), such as lipopolysaccharides (LPS), early in life, may be regarded as one of the causal factors of the increasing global increase in the incidence of autoimmune diseases, such as type 1 diabetes (T1D). Previously, a reduced incidence of T1D accompanied by dramatically increased abundances of both the mucin-metabolising bacterium , and LPS-carrying Proteobacteria was observed, when vancomycin was given to pups of nonobese diabetic (NOD) mice. While the T1D incidence reducing effect of . has been shown in further studies, little is known as to whether the increased abundance of LPS-carrying bacteria also has a protective effect. Therefore, we fed NOD pups with LPS orally from birth to weaning, which decreased the gene expressions of , , , , , , , and in the pancreatic lymph nodes, while the same gene expression profile in the spleen was unaffected. However, no significant difference in the incidence of T1D, gut microbiota composition, or ileum expression of the genetic markers of gut permeability, , , -, , , and were observed in relation to LPS ingestion. It is, therefore, concluded that early life oral . LPS has an impact on the local immune response, which, however, did not influence T1D incidence in NOD mice later in life.

摘要

在生命早期缺乏免疫系统与微生物相关分子模式(MAMPs)之间的初始接触,例如脂多糖(LPS),可能被认为是全球自身免疫性疾病(如 1 型糖尿病(T1D))发病率不断增加的一个原因。此前,当给予非肥胖型糖尿病(NOD)小鼠的幼崽万古霉素时,观察到 T1D 的发病率降低,同时黏蛋白代谢细菌和携带 LPS 的变形菌的丰度显著增加。虽然已经在进一步的研究中证明了 的 T1D 发病率降低作用,但对于携带 LPS 的细菌丰度增加是否也具有保护作用知之甚少。因此,我们从出生到断奶期间给 NOD 幼崽口服 LPS,这降低了胰腺淋巴结中 、 、 、 、 、 和 的基因表达,而脾脏中的相同基因表达谱不受影响。然而,与 LPS 摄入相关,在 T1D 发病率、肠道微生物群落组成或回肠肠道通透性的遗传标志物 、 、 - 、 、 和 的表达方面,未观察到显著差异。因此,结论是,生命早期口服 LPS 对局部免疫反应有影响,但这并没有影响 NOD 小鼠以后的 T1D 发病率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f645/6431374/45f2e5ca5a03/JDR2019-1649279.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f645/6431374/9fc934a8e933/JDR2019-1649279.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f645/6431374/2f058969f6d1/JDR2019-1649279.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f645/6431374/70abaf46c2a1/JDR2019-1649279.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f645/6431374/45f2e5ca5a03/JDR2019-1649279.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f645/6431374/9fc934a8e933/JDR2019-1649279.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f645/6431374/2f058969f6d1/JDR2019-1649279.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f645/6431374/70abaf46c2a1/JDR2019-1649279.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f645/6431374/45f2e5ca5a03/JDR2019-1649279.004.jpg

相似文献

1
Oral LPS Dosing Induces Local Immunological Changes in the Pancreatic Lymph Nodes in Mice.口服 LPS 给药可诱导小鼠胰腺淋巴结局部免疫变化。
J Diabetes Res. 2019 Mar 6;2019:1649279. doi: 10.1155/2019/1649279. eCollection 2019.
2
Modulation of Gut Microbiota by Low Methoxyl Pectin Attenuates Type 1 Diabetes in Non-obese Diabetic Mice.低甲氧基果胶通过调节肠道微生物群减轻非肥胖型糖尿病小鼠的 1 型糖尿病。
Front Immunol. 2019 Jul 30;10:1733. doi: 10.3389/fimmu.2019.01733. eCollection 2019.
3
Specific inulin-type fructan fibers protect against autoimmune diabetes by modulating gut immunity, barrier function, and microbiota homeostasis.特定的菊粉型果聚糖纤维通过调节肠道免疫、屏障功能和微生物组平衡来预防自身免疫性糖尿病。
Mol Nutr Food Res. 2017 Aug;61(8). doi: 10.1002/mnfr.201601006. Epub 2017 Mar 24.
4
A diet enriched in omega-3 PUFA and inulin prevents type 1 diabetes by restoring gut barrier integrity and immune homeostasis in NOD mice.富含 ω-3PUFA 和菊粉的饮食可通过恢复 NOD 小鼠的肠道屏障完整性和免疫稳态来预防 1 型糖尿病。
Front Immunol. 2023 Jan 13;13:1089987. doi: 10.3389/fimmu.2022.1089987. eCollection 2022.
5
Prevention of diabetes in the nonobese diabetic mouse by oral immunological treatments. Comparative efficiency of human insulin and two bacterial antigens, lipopolysacharide from Escherichia coli and glycoprotein extract from Klebsiella pneumoniae.通过口服免疫疗法预防非肥胖糖尿病小鼠患糖尿病。人胰岛素与两种细菌抗原(大肠杆菌脂多糖和肺炎克雷伯菌糖蛋白提取物)的比较效果。
Diabetes Metab. 1996 Oct;22(5):341-8.
6
Frontline Science: Abnormalities in the gut mucosa of non-obese diabetic mice precede the onset of type 1 diabetes.前沿科学:非肥胖型糖尿病小鼠的肠道黏膜异常先于 1 型糖尿病的发生。
J Leukoc Biol. 2019 Sep;106(3):513-529. doi: 10.1002/JLB.3HI0119-024RR. Epub 2019 Jul 16.
7
Early-life exposure to gut microbiota from disease-protected mice does not impact disease outcome in type 1 diabetes susceptible NOD mice.生命早期暴露于来自疾病保护型小鼠的肠道微生物群不会影响易患 1 型糖尿病的 NOD 小鼠的疾病结局。
Immunol Cell Biol. 2019 Jan;97(1):97-103. doi: 10.1111/imcb.12201. Epub 2018 Oct 9.
8
Upregulating CD4+CD25+FOXP3+ regulatory T cells in pancreatic lymph nodes in diabetic NOD mice by adjuvant immunotherapy.通过辅助免疫疗法上调糖尿病NOD小鼠胰腺淋巴结中的CD4+CD25+FOXP3+调节性T细胞。
Transplantation. 2009 Jan 27;87(2):198-206. doi: 10.1097/TP.0b013e3181933261.
9
Antibiotics in early life alter the gut microbiome and increase disease incidence in a spontaneous mouse model of autoimmune insulin-dependent diabetes.早期使用抗生素会改变肠道微生物群,并增加自身免疫性胰岛素依赖型糖尿病自发小鼠模型中的疾病发生率。
PLoS One. 2015 May 13;10(5):e0125448. doi: 10.1371/journal.pone.0125448. eCollection 2015.
10
Administration of Human Derived Upper gut Commensal Prevotella histicola delays the onset of type 1 diabetes in NOD mice.普氏粪杆菌定植可延缓 NOD 小鼠 1 型糖尿病的发生。
BMC Microbiol. 2022 Jan 4;22(1):8. doi: 10.1186/s12866-021-02406-9.

引用本文的文献

1
The biofunction of in intestinal-related diseases.[具体物质]在肠道相关疾病中的生物功能。 (原文中“of”后面缺少具体内容)
Microbiome Res Rep. 2024 Sep 5;3(4):47. doi: 10.20517/mrr.2024.12. eCollection 2024.
2
Oral route lipopolysaccharide as a potential dementia preventive agent inducing neuroprotective microglia.口服脂多糖作为一种有潜力的预防痴呆症的药物,可诱导神经保护型小胶质细胞。
Front Immunol. 2023 Mar 9;14:1110583. doi: 10.3389/fimmu.2023.1110583. eCollection 2023.
3
Microbiota-dependent proteolysis of gluten subverts diet-mediated protection against type 1 diabetes.

本文引用的文献

1
Dietary LPS traces influences disease expression of the diet-induced obese mouse.膳食中脂多糖痕迹影响饮食诱导肥胖小鼠的疾病表现。
Res Vet Sci. 2019 Apr;123:195-203. doi: 10.1016/j.rvsc.2019.01.005. Epub 2019 Jan 8.
2
The gut microbiota metabolite indole alleviates liver inflammation in mice.肠道微生物群代谢产物吲哚可减轻小鼠肝脏炎症。
FASEB J. 2018 Jun 15;32(12):fj201800544. doi: 10.1096/fj.201800544.
3
Akkermansia muciniphila can reduce the damage of gluco/lipotoxicity, oxidative stress and inflammation, and normalize intestine microbiota in streptozotocin-induced diabetic rats.
微生物群依赖的麸质蛋白水解作用破坏了饮食介导的对 1 型糖尿病的保护作用。
Cell Host Microbe. 2023 Feb 8;31(2):213-227.e9. doi: 10.1016/j.chom.2022.12.009. Epub 2023 Jan 4.
4
The Role of the Gut Microbiota in the Pathogenesis of Diabetes.肠道微生物群在糖尿病发病机制中的作用。
Int J Mol Sci. 2022 Jan 1;23(1):480. doi: 10.3390/ijms23010480.
5
Gut microbiota and diabetes: From correlation to causality and mechanism.肠道微生物群与糖尿病:从相关性到因果关系及机制
World J Diabetes. 2020 Jul 15;11(7):293-308. doi: 10.4239/wjd.v11.i7.293.
6
Therapeutic Effect of Bifidobacterium Administration on Experimental Autoimmune Myasthenia Gravis in Lewis Rats.双歧杆菌对实验性自身免疫性重症肌无力大鼠的治疗作用。
Front Immunol. 2019 Dec 19;10:2949. doi: 10.3389/fimmu.2019.02949. eCollection 2019.
阿克曼氏菌(Akkermansia muciniphila)可减轻糖脂毒性、氧化应激和炎症对机体的损伤,并可使链脲佐菌素诱导的糖尿病大鼠肠道微生物群恢复正常。
Pathog Dis. 2018 Jun 1;76(4). doi: 10.1093/femspd/fty028.
4
An Early Life Mucosal Insult Temporarily Decreases Acute Oxazolone-Induced Inflammation in Mice.早期生活黏膜损伤可暂时减轻小鼠急性氧化唑诱导的炎症。
Inflammation. 2018 Aug;41(4):1437-1447. doi: 10.1007/s10753-018-0790-y.
5
induces gut microbiota remodelling and controls islet autoimmunity in NOD mice.诱导肠道微生物群重塑并控制 NOD 小鼠的胰岛自身免疫。
Gut. 2018 Aug;67(8):1445-1453. doi: 10.1136/gutjnl-2017-314508. Epub 2017 Dec 21.
6
Effect of Early-life Gut Mucosal Compromise on Disease Progression in NOD Mice.早期肠道黏膜受损对非肥胖糖尿病(NOD)小鼠疾病进展的影响。
Comp Med. 2017 Oct 1;67(5):388-399.
7
Regulation of type 1 diabetes development and B-cell activation in nonobese diabetic mice by early life exposure to a diabetogenic environment.早年暴露于致糖尿病环境对非肥胖糖尿病小鼠1型糖尿病发展和B细胞激活的调节作用。
PLoS One. 2017 Aug 3;12(8):e0181964. doi: 10.1371/journal.pone.0181964. eCollection 2017.
8
Immunological effects of reduced mucosal integrity in the early life of BALB/c mice.BALB/c小鼠生命早期黏膜完整性降低的免疫效应
PLoS One. 2017 May 1;12(5):e0176662. doi: 10.1371/journal.pone.0176662. eCollection 2017.
9
Sensitivity to oxazolone induced dermatitis is transferable with gut microbiota in mice.对恶唑酮诱导的皮炎的敏感性可通过肠道微生物群在小鼠中传递。
Sci Rep. 2017 Mar 14;7:44385. doi: 10.1038/srep44385.
10
Microbiota Influences Vaccine and Mucosal Adjuvant Efficacy.微生物群影响疫苗和黏膜佐剂的功效。
Immune Netw. 2017 Feb;17(1):20-24. doi: 10.4110/in.2017.17.1.20. Epub 2017 Feb 23.