• 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

相似文献

1
Immunological goings-on in visceral adipose tissue.内脏脂肪组织中的免疫活动。
Cell Metab. 2013 Jun 4;17(6):851-859. doi: 10.1016/j.cmet.2013.05.008.
2
The "Big Bang" in obese fat: Events initiating obesity-induced adipose tissue inflammation.肥胖脂肪中的“大爆炸”:引发肥胖诱导的脂肪组织炎症的事件。
Eur J Immunol. 2015 Sep;45(9):2446-56. doi: 10.1002/eji.201545502. Epub 2015 Aug 19.
3
Ambient air pollution exaggerates adipose inflammation and insulin resistance in a mouse model of diet-induced obesity.在饮食诱导肥胖的小鼠模型中,环境空气污染会加剧脂肪炎症和胰岛素抵抗。
Circulation. 2009 Feb 3;119(4):538-46. doi: 10.1161/CIRCULATIONAHA.108.799015. Epub 2009 Jan 19.
4
B Lymphocytes in obesity-related adipose tissue inflammation and insulin resistance.肥胖相关脂肪组织炎症和胰岛素抵抗中的 B 淋巴细胞。
Cell Mol Life Sci. 2014 Mar;71(6):1033-43. doi: 10.1007/s00018-013-1486-y. Epub 2013 Oct 15.
5
T-lymphocyte infiltration in visceral adipose tissue: a primary event in adipose tissue inflammation and the development of obesity-mediated insulin resistance.内脏脂肪组织中的T淋巴细胞浸润:脂肪组织炎症和肥胖介导的胰岛素抵抗发生发展中的首要事件。
Arterioscler Thromb Vasc Biol. 2008 Jul;28(7):1304-10. doi: 10.1161/ATVBAHA.108.165100. Epub 2008 Apr 17.
6
Regulation of adipose tissue T cell subsets by Stat3 is crucial for diet-induced obesity and insulin resistance.Stat3 调控脂肪组织 T 细胞亚群对于饮食诱导的肥胖和胰岛素抵抗至关重要。
Proc Natl Acad Sci U S A. 2013 Aug 6;110(32):13079-84. doi: 10.1073/pnas.1311557110. Epub 2013 Jul 22.
7
NK cells link obesity-induced adipose stress to inflammation and insulin resistance.自然杀伤细胞将肥胖引起的脂肪组织应激与炎症和胰岛素抵抗联系起来。
Nat Immunol. 2015 Apr;16(4):376-85. doi: 10.1038/ni.3120. Epub 2015 Mar 2.
8
Adaptive immunity in obesity and insulin resistance.肥胖与胰岛素抵抗中的适应性免疫。
Nat Rev Endocrinol. 2012 Dec;8(12):709-16. doi: 10.1038/nrendo.2012.114. Epub 2012 Jul 31.
9
Adipose tissue lymphocytes and macrophages in obesity and insulin resistance: makers or markers, and which comes first?肥胖与胰岛素抵抗中的脂肪组织淋巴细胞和巨噬细胞:制造者还是标志物,何者为先?
Arterioscler Thromb Vasc Biol. 2008 Jul;28(7):1211-3. doi: 10.1161/ATVBAHA.108.168229.
10
The B-side story in insulin resistance.
Nat Med. 2011 May;17(5):539-40. doi: 10.1038/nm0511-539.

引用本文的文献

1
Transcriptome and Cellular Evidence of Depot-Specific Function in Beef Cattle Intramuscular, Subcutaneous, and Visceral Adipose Tissues.肉牛肌内、皮下和内脏脂肪组织中特定部位功能的转录组和细胞证据
Biology (Basel). 2025 Jul 11;14(7):848. doi: 10.3390/biology14070848.
2
Regulatory T cells in brown adipose tissue safeguard thermogenesis by restraining interferon-γ-producing lymphocytes.棕色脂肪组织中的调节性T细胞通过抑制产生干扰素-γ的淋巴细胞来保护产热。
Sci Immunol. 2025 Jul 25;10(109):eads0478. doi: 10.1126/sciimmunol.ads0478.
3
Adipose tissue harbors pathogenic T cells in obesity that exacerbate inflammatory arthritis.在肥胖症中,脂肪组织含有致病性T细胞,会加剧炎症性关节炎。
J Exp Med. 2025 Sep 1;222(9). doi: 10.1084/jem.20240677. Epub 2025 Jul 7.
4
Immune cell-adipose tissue crosstalk in metabolic diseases with a focus on type 1 diabetes.免疫细胞与脂肪组织在代谢性疾病中的相互作用,重点关注1型糖尿病
Diabetologia. 2025 Jun 4. doi: 10.1007/s00125-025-06437-z.
5
Lipid accumulation product and visceral adiposity index as independent predictors of long-term survival after gastric cancer immunotherapy.脂质蓄积产物和内脏脂肪指数作为胃癌免疫治疗后长期生存的独立预测因素。
BMC Cancer. 2025 Jun 5;25(1):1009. doi: 10.1186/s12885-025-14411-6.
6
Paradoxical effects of adiposity and inflammation on immunotherapy efficacy in gastric cancer: novel insights from real-world data.肥胖和炎症对胃癌免疫治疗疗效的矛盾影响:来自真实世界数据的新见解
Gastric Cancer. 2025 May 12. doi: 10.1007/s10120-025-01622-w.
7
Interleukin-33 and Obesity-Related Inflammation and Cancer.白细胞介素-33与肥胖相关炎症及癌症
Encyclopedia (Basel, 2021). 2024 Dec;4(4):1770-1789. doi: 10.3390/encyclopedia4040117. Epub 2024 Nov 23.
8
Gut Microbiota-Butyrate-PPARγ Axis Modulates Adipose Regulatory T Cell Population.肠道微生物群-丁酸盐-PPARγ轴调节脂肪组织调节性T细胞群体。
Adv Sci (Weinh). 2025 May;12(20):e2411086. doi: 10.1002/advs.202411086. Epub 2025 Feb 25.
9
Siglec-E augments adipose tissue inflammation by modulating TRAF3 signaling and monocytic myeloid-derived suppressor cells during obesity.在肥胖过程中,唾液酸结合免疫球蛋白样凝集素E(Siglec-E)通过调节TRAF3信号传导和单核细胞来源的髓源性抑制细胞来增强脂肪组织炎症。
Front Immunol. 2025 Feb 4;16:1501307. doi: 10.3389/fimmu.2025.1501307. eCollection 2025.
10
Macrophage SUCLA2 coupled glutaminolysis manipulates obesity through AMPK.巨噬细胞SUCLA2偶联的谷氨酰胺分解通过AMPK调控肥胖。
Nat Commun. 2025 Feb 18;16(1):1738. doi: 10.1038/s41467-025-57044-w.

本文引用的文献

1
Lack of invariant natural killer T cells affects lipid metabolism in adipose tissue of diet-induced obese mice.缺乏不变自然杀伤 T 细胞会影响饮食诱导肥胖小鼠脂肪组织中的脂质代谢。
Arterioscler Thromb Vasc Biol. 2013 Jun;33(6):1189-96. doi: 10.1161/ATVBAHA.112.301105. Epub 2013 Mar 21.
2
Adipose tissue macrophages function as antigen-presenting cells and regulate adipose tissue CD4+ T cells in mice.脂肪组织巨噬细胞作为抗原呈递细胞在调节小鼠脂肪组织 CD4+T 细胞中发挥作用。
Diabetes. 2013 Aug;62(8):2762-72. doi: 10.2337/db12-1404. Epub 2013 Mar 14.
3
B cells promote inflammation in obesity and type 2 diabetes through regulation of T-cell function and an inflammatory cytokine profile.B 细胞通过调节 T 细胞功能和炎症细胞因子谱促进肥胖和 2 型糖尿病中的炎症反应。
Proc Natl Acad Sci U S A. 2013 Mar 26;110(13):5133-8. doi: 10.1073/pnas.1215840110. Epub 2013 Mar 11.
4
Class II major histocompatibility complex plays an essential role in obesity-induced adipose inflammation.Ⅱ类主要组织相容性复合体在肥胖诱导的脂肪炎症中起着至关重要的作用。
Cell Metab. 2013 Mar 5;17(3):411-22. doi: 10.1016/j.cmet.2013.02.009.
5
Innate lymphoid type 2 cells sustain visceral adipose tissue eosinophils and alternatively activated macrophages.先天淋巴样细胞 2 型维持内脏脂肪组织嗜酸性粒细胞和选择性激活的巨噬细胞。
J Exp Med. 2013 Mar 11;210(3):535-49. doi: 10.1084/jem.20121964. Epub 2013 Feb 18.
6
A T-bet gradient controls the fate and function of CCR6-RORγt+ innate lymphoid cells.T 细胞特异性转录因子(T-bet)梯度控制 CCR6+RORγt+固有淋巴细胞的命运和功能。
Nature. 2013 Feb 14;494(7436):261-5. doi: 10.1038/nature11813. Epub 2013 Jan 16.
7
Recognition of CD1d-restricted antigens by natural killer T cells.自然杀伤 T 细胞识别 CD1d 限制性抗原。
Nat Rev Immunol. 2012 Dec;12(12):845-57. doi: 10.1038/nri3328. Epub 2012 Nov 16.
8
A guanidine-rich regulatory oligodeoxynucleotide improves type-2 diabetes in obese mice by blocking T-cell differentiation.一种富含胍基的调节性寡脱氧核苷酸通过阻断 T 细胞分化改善肥胖小鼠的 2 型糖尿病。
EMBO Mol Med. 2012 Oct;4(10):1112-25. doi: 10.1002/emmm.201201272.
9
Adipose tissue invariant NKT cells protect against diet-induced obesity and metabolic disorder through regulatory cytokine production.脂肪组织不变自然杀伤 T 细胞通过调节细胞因子的产生来预防饮食诱导的肥胖和代谢紊乱。
Immunity. 2012 Sep 21;37(3):574-87. doi: 10.1016/j.immuni.2012.06.016. Epub 2012 Sep 13.
10
Neutrophils mediate insulin resistance in mice fed a high-fat diet through secreted elastase.中性粒细胞通过分泌弹性蛋白酶介导高脂饮食喂养的小鼠胰岛素抵抗。
Nat Med. 2012 Sep;18(9):1407-12. doi: 10.1038/nm.2885.

内脏脂肪组织中的免疫活动。

Immunological goings-on in visceral adipose tissue.

机构信息

Division of Immunology, Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Cell Metab. 2013 Jun 4;17(6):851-859. doi: 10.1016/j.cmet.2013.05.008.

DOI:10.1016/j.cmet.2013.05.008
PMID:23747244
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4264591/
Abstract

Chronic, low-grade inflammation of visceral adipose tissue, and systemically, is a critical link between recent strikingly parallel rises in the incidence of obesity and type 2 diabetes. Macrophages have been recognized for some time to be critical participants in obesity-induced inflammation of adipose tissue. Of late, a score of other cell types of the innate and adaptive arms of the immune system have been suggested to play a positive or negative role in adipose tissue infiltrates. This piece reviews the existing data on these new participants; discusses experimental uncertainties, inconsistencies, and complexities; and puts forward a minimalist synthetic scheme.

摘要

内脏脂肪组织的慢性、低度炎症,以及全身性炎症,是肥胖症和 2 型糖尿病发病率近期惊人平行上升之间的关键环节。巨噬细胞一直被认为是肥胖引起的脂肪组织炎症的关键参与者。最近,许多其他先天和适应性免疫系统的细胞类型被认为在脂肪组织浸润中发挥积极或消极作用。本文回顾了这些新参与者的现有数据;讨论了实验中的不确定性、不一致性和复杂性;并提出了一个最小综合方案。