SIRT6 和 NMNAT2 的下调与增殖性糖尿病视网膜病变有关。

IF 1.8 3区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Vision Pub Date : 2023-10-02 eCollection Date: 2023-01-01
Hui Chen, Xiongze Zhang, Nanying Liao, Yuying Ji, Lan Mi, Yuhong Gan, Yongyue Su, Feng Wen
{"title":"SIRT6 和 NMNAT2 的下调与增殖性糖尿病视网膜病变有关。","authors":"Hui Chen, Xiongze Zhang, Nanying Liao, Yuying Ji, Lan Mi, Yuhong Gan, Yongyue Su, Feng Wen","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To determine the expression levels of <i>SIRT6</i> and <i>NMNAT2</i> in diabetic retinopathy (DR).</p><p><strong>Methods: </strong>We obtained peripheral blood mononuclear cells (PBMCs) and vitreous samples from 77 patients with type 2 diabetes mellitus: 52 with DR and 25 without DR, and 27 healthy control subjects. Western blot analysis and qRT-PCR were performed to evaluate the expression of <i>SIRT6</i> and <i>NMNAT2</i> in their PBMCs. The levels of <i>IL-1β</i>, <i>IL-6</i>, and <i>TNF-α</i> in the vitreous fluid were determined by ELISA. Immunohistochemistry was performed to detect the expression of <i>SIRT6</i> and <i>NMNAT</i>2 in proliferative DR (PDR) and the control subjects.</p><p><strong>Results: </strong>The expression of <i>SIRT6</i> and <i>NMNAT2</i> was markedly downregulated in DR patients, which was negatively correlated with the increased expression of <i>IL-1β, IL-6</i> and <i>TNF-α</i>. Additionally, we observed decreased expression of <i>SIRT6</i> and <i>NMNAT2</i> in the fibrovascular membranes of PDR patients.</p><p><strong>Conclusions: </strong>The downregulated expression of <i>SIRT6</i> and <i>NMNAT2</i> in PDR patients reveals a potential pathogenic association; more extended studies could verify them as potential therapeutic targets.</p>","PeriodicalId":18866,"journal":{"name":"Molecular Vision","volume":"29 ","pages":"160-168"},"PeriodicalIF":1.8000,"publicationDate":"2023-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10784219/pdf/","citationCount":"0","resultStr":"{\"title\":\"Downregulation of SIRT6 and NMNAT2 is associated with proliferative diabetic retinopathy.\",\"authors\":\"Hui Chen, Xiongze Zhang, Nanying Liao, Yuying Ji, Lan Mi, Yuhong Gan, Yongyue Su, Feng Wen\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>To determine the expression levels of <i>SIRT6</i> and <i>NMNAT2</i> in diabetic retinopathy (DR).</p><p><strong>Methods: </strong>We obtained peripheral blood mononuclear cells (PBMCs) and vitreous samples from 77 patients with type 2 diabetes mellitus: 52 with DR and 25 without DR, and 27 healthy control subjects. Western blot analysis and qRT-PCR were performed to evaluate the expression of <i>SIRT6</i> and <i>NMNAT2</i> in their PBMCs. The levels of <i>IL-1β</i>, <i>IL-6</i>, and <i>TNF-α</i> in the vitreous fluid were determined by ELISA. Immunohistochemistry was performed to detect the expression of <i>SIRT6</i> and <i>NMNAT</i>2 in proliferative DR (PDR) and the control subjects.</p><p><strong>Results: </strong>The expression of <i>SIRT6</i> and <i>NMNAT2</i> was markedly downregulated in DR patients, which was negatively correlated with the increased expression of <i>IL-1β, IL-6</i> and <i>TNF-α</i>. Additionally, we observed decreased expression of <i>SIRT6</i> and <i>NMNAT2</i> in the fibrovascular membranes of PDR patients.</p><p><strong>Conclusions: </strong>The downregulated expression of <i>SIRT6</i> and <i>NMNAT2</i> in PDR patients reveals a potential pathogenic association; more extended studies could verify them as potential therapeutic targets.</p>\",\"PeriodicalId\":18866,\"journal\":{\"name\":\"Molecular Vision\",\"volume\":\"29 \",\"pages\":\"160-168\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2023-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10784219/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Vision\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Vision","FirstCategoryId":"3","ListUrlMain":"","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

目的:测定糖尿病视网膜病变(DR)中 SIRT6 和 NMNAT2 的表达水平:我们采集了 77 名 2 型糖尿病患者的外周血单核细胞(PBMC)和玻璃体样本:方法:我们采集了 77 名 2 型糖尿病患者的外周血单核细胞(PBMC)和玻璃体样本,其中 52 人患有 DR,25 人未患 DR,另外还有 27 名健康对照者。研究人员采用 Western 印迹分析和 qRT-PCR 技术评估了患者 PBMCs 中 SIRT6 和 NMNAT2 的表达情况。玻璃体液中的 IL-1β、IL-6 和 TNF-α 水平是通过 ELISA 法测定的。免疫组化法检测增殖性DR(PDR)和对照组中SIRT6和NMNAT2的表达:结果:SIRT6和NMNAT2的表达在DR患者中明显下调,这与IL-1β、IL-6和TNF-α的表达增加呈负相关。此外,我们还观察到SIRT6和NMNAT2在PDR患者纤维血管膜中的表达下降:结论:SIRT6和NMNAT2在PDR患者中的表达下调揭示了一种潜在的致病关联;更多的扩展研究可以验证它们是潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Downregulation of SIRT6 and NMNAT2 is associated with proliferative diabetic retinopathy.

Purpose: To determine the expression levels of SIRT6 and NMNAT2 in diabetic retinopathy (DR).

Methods: We obtained peripheral blood mononuclear cells (PBMCs) and vitreous samples from 77 patients with type 2 diabetes mellitus: 52 with DR and 25 without DR, and 27 healthy control subjects. Western blot analysis and qRT-PCR were performed to evaluate the expression of SIRT6 and NMNAT2 in their PBMCs. The levels of IL-1β, IL-6, and TNF-α in the vitreous fluid were determined by ELISA. Immunohistochemistry was performed to detect the expression of SIRT6 and NMNAT2 in proliferative DR (PDR) and the control subjects.

Results: The expression of SIRT6 and NMNAT2 was markedly downregulated in DR patients, which was negatively correlated with the increased expression of IL-1β, IL-6 and TNF-α. Additionally, we observed decreased expression of SIRT6 and NMNAT2 in the fibrovascular membranes of PDR patients.

Conclusions: The downregulated expression of SIRT6 and NMNAT2 in PDR patients reveals a potential pathogenic association; more extended studies could verify them as potential therapeutic targets.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Molecular Vision
Molecular Vision 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
25
审稿时长
1 months
期刊介绍: Molecular Vision is a peer-reviewed journal dedicated to the dissemination of research results in molecular biology, cell biology, and the genetics of the visual system (ocular and cortical). Molecular Vision publishes articles presenting original research that has not previously been published and comprehensive articles reviewing the current status of a particular field or topic. Submissions to Molecular Vision are subjected to rigorous peer review. Molecular Vision does NOT publish preprints. For authors, Molecular Vision provides a rapid means of communicating important results. Access to Molecular Vision is free and unrestricted, allowing the widest possible audience for your article. Digital publishing allows you to use color images freely (and without fees). Additionally, you may publish animations, sounds, or other supplementary information that clarifies or supports your article. Each of the authors of an article may also list an electronic mail address (which will be updated upon request) to give interested readers easy access to authors.
期刊最新文献
Erratum: A method for gene knockdown in the retina using a lipid-based carrier. Increased inflammatory mediators in the ocular surface tissue in keratoconus. Retraction: Swati Arora, Nagendra Verma. Exosomal microRNAs as potential biomarkers and therapeutic targets in corneal diseases. Molecular Vision 2024; 30:92-106. Complement C3 is downregulated following ranibizumab intervention in experimental central retinal vein occlusion. A potential novel role of the R36P mutation in CRYGD in congenial cataract.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1