SRT1720对瘢痕成纤维细胞的调控作用

被引:0
作者
严艺文 [1 ,2 ]
张婷 [1 ]
郑朝 [1 ]
机构
[1] 空军军医大学第一附属医院烧伤与皮肤外科
[2] 空军军医大学基础医学院六大队
关键词
瘢痕成纤维细胞; Ⅰ型胶原蛋白; α-平滑肌肌动蛋白;
D O I
暂无
中图分类号
R622 [整形手术学];
学科分类号
1002 ; 100210 ;
摘要
目的 研究沉默信息调节因子1(silence information regulator 1,SIRT1)的激动剂SRT1720对增生性瘢痕成纤维细胞表型的调控作用。方法 自2022年1—6月,空军军医大学第一附属医院烧伤与皮肤外科将瘢痕真皮成纤维细胞(hypertrophic scar fibroblasts,HSF)按随机数字表法分为PBS对照组与SRT1720处理组,样本数9个/组。先分别用等量PBS与终浓度为2μmol/L的SRT1720处理HSF 24 h,然后分别采用实时荧光定量反转录PCR(RT-PCR)法检测HSF中Ⅰ型胶原蛋白(CollagenⅠ)和α-平滑肌肌动蛋白(α-SMA)的m RNA表达水平差异,采用蛋白质印迹法检测HSF中CollagenⅠ和α-SMA的蛋白表达水平差异;采用免疫荧光法检测两组CollagenⅠ和α-SMA在HSF中的胞内表达与定位情况。以上3种细胞实验中每组样本数均为3个。采用GraphPad Prim 8.0进行数据统计分析,组间数据比较采用独立样本t检验,P<0.05为差异有统计学意义。结果 SRT1720处理组HSF中CollagenⅠ与α-SMA的m RNA表达量分别为(0.34±0.06)、(0.43±0.08),均明显低于PBS对照组(1.00±0.12)、(1.00±0.13),t值分别为8.57、6.79,P<0.01;经SRT1720处理HSF的CollagenⅠ与α-SMA的蛋白表达量(0.70±0.05)、(0.64±0.09),均明显少于PBS对照组的(1.14±0.04)、(1.10±0.05),t值分别为12.61、7.37,P<0.01。免疫荧光染色显示,CollagenⅠ与α-SMA主要定位在HSF的细胞质,SRT1720处理组CollagenⅠ与α-SMA的表达量较PBS对照组减少。结论 SRT1720能够通过激活SIRT1显著抑制瘢痕成纤维细胞CollagenⅠ与α-SMA表达,从而抑制细胞外基质(extracellular matrix,ECM)合成与成纤维细胞的异常转分化。
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页码:395 / 398
页数:4
相关论文
共 13 条
[1]   Insufficient SIRT1 in macrophages promotes oxidative stress and inflammation during scarring [J].
He, Ting ;
Bai, Xiaozhi ;
Li, Yan ;
Zhang, Dongliang ;
Xu, Zhigang ;
Yang, Xuekang ;
Hu, Dahai ;
Han, Juntao .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2023, 101 (11) :1397-1407
[2]  
The Role of Myofibroblasts in Physiological and Pathological Tissue Repair..[J].Schuster Ronen;Younesi Fereshteh;Ezzo Maya;Hinz Boris.Cold Spring Harbor perspectives in biology.2022, 1
[3]  
Exosome Derived from Mesenchymal Stem Cells Alleviates Pathological Scars by Inhibiting the Proliferation; Migration and Protein Expression of Fibroblasts via Delivering miR-138-5p to Target SIRT1.[J].Zhao;Zhang;Zang;Zhang;Zhao;Li;Yang;Feng;Zhang;Cui.International Journal of Nanomedicine.2022,
[4]   Sirt1 overexpression improves senescence-associated pulmonary fibrosis induced by vitamin D deficiency through downregulating IL-11 transcription [J].
Zhou, Jiawen ;
Chen, Haiyun ;
Wang, Qiuyi ;
Chen, Sihan ;
Wang, Rong ;
Wang, Ziyang ;
Yang, Cuicui ;
Chen, Ao ;
Zhao, Jingyu ;
Zhou, Zihao ;
Mao, Zhiyuan ;
Zuo, Guoping ;
Miao, Dengshun ;
Jin, Jianliang .
AGING CELL, 2022, 21 (08)
[5]  
The Most Current Algorithms for the Treatment and Prevention of Hypertrophic Scars and Keloids: A 2020 Update of the Algorithms Published 10 Years Ago.[J].Ogawa Rei.Plastic & Reconstructive Surgery.2021,
[6]   LncRNA PICSAR binds to miR-485-5p and activates TGF-β1/Smad to promote abnormal proliferation of hypertrophic scar fibroblasts (HSFs) and excessive deposition of extracellular matrix (ECM) [J].
Xu, Sijia ;
Dong, Wenxin ;
Shi, Yu .
MEDICAL MOLECULAR MORPHOLOGY, 2021, 54 (04) :337-345
[7]  
The Biology of Extracellular Matrix Proteins in Hypertrophic Scarring..[J].Eremenko Elizabeth;Ding Jie;Kwan Peter;Tredget Edward E.Advances in wound care.2021, 5
[8]   SIRT1 attenuates renal fibrosis by repressing HIF-2α [J].
Li, Peipei ;
Liu, Yue ;
Qin, Xiaogang ;
Chen, Kairen ;
Wang, Ruiting ;
Yuan, Li ;
Chen, Xiaolan ;
Hao, Chuanming ;
Huang, Xinzhong .
CELL DEATH DISCOVERY, 2021, 7 (01)
[9]  
Fibroblast contributions to ischemic cardiac remodeling.[J].Burke Ryan M.;Burgos Villar Kimberly N.;Small Eric M..Cellular Signalling.2021, prepublish
[10]   Relevance of SIRT1-NF-κB Axis as Therapeutic Target to Ameliorate Inflammation in Liver Disease [J].
de Gregorio, Estefania ;
Cole, Anna ;
Morales, Albert ;
Mari, Montserrat .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (11) :1-24