• 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

维生素 D 通过下调糖尿病肾病大鼠 TREM-1 抑制巨噬细胞浸润。

Vitamin D suppresses macrophage infiltration by down-regulation of TREM-1 in diabetic nephropathy rats.

机构信息

Institute of Nephrology, Zhong Da Hospital, Southeast University, School of Medicine, Nanjing, Jiangsu, 210009, China.

Institute of Nephrology, Zhong Da Hospital, Southeast University, School of Medicine, Nanjing, Jiangsu, 210009, China.

出版信息

Mol Cell Endocrinol. 2018 Sep 15;473:44-52. doi: 10.1016/j.mce.2018.01.001. Epub 2018 Jan 10.

DOI:10.1016/j.mce.2018.01.001
PMID:29331667
Abstract

This study intends to investigate the effect of active vitamin D (VD) on the expression of triggering receptor expressed on myeloid cells-1 (TREM-1) in the renal tissues of diabetic nephropathy (DN) rats and to explore the impact of TREM-1 on macrophage adhesion and migration. We find that the expressions of TREM-1 and CD68 protein are higher in DN rats compared with rats in the normal control group and that these changes are decreased in the DN + VD group. In vitro, the capacity for macrophage adhesion and migration and the expression of TREM-1 are increased under high-glucose conditions, but VD inhibits this progress. TREM-1 siRNA decreases high-glucose-induced macrophage adhesion and migration, whereas over-expression of TREM-1 inhibits its action. However, VD cannot suppress high glucose-induced TREM-1 expression and macrophage adhesion and migration when TREM-1 is over-expressed. These results demonstrate that VD can suppress macrophage adhesion and migration by reducing the expression of TREM-1.

摘要

本研究旨在探讨活性维生素 D(VD)对糖尿病肾病(DN)大鼠肾组织中髓系细胞触发受体-1(TREM-1)表达的影响,并探讨 TREM-1对巨噬细胞黏附和迁移的影响。我们发现,与正常对照组大鼠相比,DN 大鼠的 TREM-1 和 CD68 蛋白表达更高,而在 DN+VD 组这些变化则减少。在体外,高糖条件下巨噬细胞黏附和迁移的能力以及 TREM-1 的表达增加,但 VD 抑制了这一过程。TREM-1 siRNA 降低高糖诱导的巨噬细胞黏附和迁移,而过表达 TREM-1 则抑制其作用。然而,当 TREM-1 过表达时,VD 不能抑制高糖诱导的 TREM-1 表达和巨噬细胞黏附和迁移。这些结果表明,VD 可以通过降低 TREM-1 的表达来抑制巨噬细胞的黏附和迁移。

相似文献

1
Vitamin D suppresses macrophage infiltration by down-regulation of TREM-1 in diabetic nephropathy rats.维生素 D 通过下调糖尿病肾病大鼠 TREM-1 抑制巨噬细胞浸润。
Mol Cell Endocrinol. 2018 Sep 15;473:44-52. doi: 10.1016/j.mce.2018.01.001. Epub 2018 Jan 10.
2
Active vitamin D regulates macrophage M1/M2 phenotypes via the STAT-1-TREM-1 pathway in diabetic nephropathy.活性维生素 D 通过 STAT-1-TREM-1 通路调节糖尿病肾病中巨噬细胞 M1/M2 表型。
J Cell Physiol. 2019 May;234(5):6917-6926. doi: 10.1002/jcp.27450. Epub 2018 Nov 27.
3
Macrophage phenotype and its relationship with renal function in human diabetic nephropathy.人糖尿病肾病中巨噬细胞表型及其与肾功能的关系。
PLoS One. 2019 Sep 11;14(9):e0221991. doi: 10.1371/journal.pone.0221991. eCollection 2019.
4
Vitamin D prevents podocyte injury via regulation of macrophage M1/M2 phenotype in diabetic nephropathy rats.维生素D通过调节糖尿病肾病大鼠巨噬细胞的M1/M2表型来预防足细胞损伤。
Endocrinology. 2014 Dec;155(12):4939-50. doi: 10.1210/en.2014-1020. Epub 2014 Sep 4.
5
Effects of autophagy on macrophage adhesion and migration in diabetic nephropathy.自噬对糖尿病肾病中巨噬细胞黏附和迁移的影响。
Ren Fail. 2019 Nov;41(1):682-690. doi: 10.1080/0886022X.2019.1632209.
6
Mitophagy regulates macrophage phenotype in diabetic nephropathy rats.线粒体自噬调节糖尿病肾病大鼠的巨噬细胞表型。
Biochem Biophys Res Commun. 2017 Dec 9;494(1-2):42-50. doi: 10.1016/j.bbrc.2017.10.088. Epub 2017 Oct 21.
7
Beyond proteinuria: VDR activation reduces renal inflammation in experimental diabetic nephropathy.超越蛋白尿:维生素 D 受体激活可减少实验性糖尿病肾病中的肾脏炎症。
Am J Physiol Renal Physiol. 2012 Mar 15;302(6):F647-57. doi: 10.1152/ajprenal.00090.2011. Epub 2011 Dec 14.
8
Triggering Receptor Expressed on Myeloid Cells-2 Expression Tracks With M2-Like Macrophage Activity and Disease Severity in COPD.髓系细胞触发受体-2 的表达与 COPD 中 M2 样巨噬细胞活性和疾病严重程度相关。
Chest. 2018 Jan;153(1):77-86. doi: 10.1016/j.chest.2017.09.044. Epub 2017 Oct 7.
9
Renal kallikrein activation and renoprotection after dual blockade of renin-angiotensin system in diet-induced diabetic nephropathy.饮食诱导的糖尿病肾病中肾素-血管紧张素系统双重阻断后肾激肽释放酶激活与肾脏保护作用
J Diabetes Res. 2015;2015:310645. doi: 10.1155/2015/310645. Epub 2015 Mar 30.
10
TREM-1 associated macrophage polarization plays a significant role in inducing insulin resistance in obese population.与触发受体表达分子-1(TREM-1)相关的巨噬细胞极化在诱导肥胖人群胰岛素抵抗中起重要作用。
J Transl Med. 2017 Apr 28;15(1):85. doi: 10.1186/s12967-017-1187-7.

引用本文的文献

1
The effect of intestinal flora metabolites on macrophage polarization.肠道菌群代谢产物对巨噬细胞极化的影响。
Heliyon. 2024 Aug 3;10(15):e35755. doi: 10.1016/j.heliyon.2024.e35755. eCollection 2024 Aug 15.
2
Role of triggering receptor expressed on myeloid cells-1 in kidney diseases: A biomarker and potential therapeutic target.触发受体表达于髓样细胞-1 在肾脏疾病中的作用:一个生物标志物和潜在的治疗靶点。
Chin Med J (Engl). 2024 Jul 20;137(14):1663-1673. doi: 10.1097/CM9.0000000000003197. Epub 2024 May 28.
3
Vascular calcification progression and its association with mineral and bone disorder in kidney transplant recipients.
血管钙化进展及其与肾移植受者矿物质和骨代谢紊乱的关系。
Ren Fail. 2023;45(2):2276382. doi: 10.1080/0886022X.2023.2276382. Epub 2023 Nov 7.
4
Relationship between Macrophages and Tissue Microenvironments in Diabetic Kidneys.糖尿病肾病中巨噬细胞与组织微环境的关系
Biomedicines. 2023 Jul 3;11(7):1889. doi: 10.3390/biomedicines11071889.
5
A Potential Role of Vitamin D on Platelet Leukocyte Aggregation and Pathological Events in Sepsis: An Updated Review.维生素D在脓毒症患者血小板白细胞聚集及病理过程中的潜在作用:最新综述
J Inflamm Res. 2021 Jul 30;14:3651-3664. doi: 10.2147/JIR.S321362. eCollection 2021.
6
Mesenchymal stem cells protect renal tubular cells via TSG-6 regulating macrophage function and phenotype switching.间充质干细胞通过 TSG-6 调节巨噬细胞功能和表型转换来保护肾小管细胞。
Am J Physiol Renal Physiol. 2021 Mar 1;320(3):F454-F463. doi: 10.1152/ajprenal.00426.2020. Epub 2021 Feb 8.
7
TREM-1; Is It a Pivotal Target for Cardiovascular Diseases?触发受体表达于髓样细胞-1;它是心血管疾病的关键靶点吗?
J Cardiovasc Dev Dis. 2018 Sep 7;5(3):45. doi: 10.3390/jcdd5030045.