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题名

SET knockdown attenuated phenotype modulation and calcium channel associated markers of airway smooth muscle cells in asthmatic mice

作者
通讯作者Li, Jie; Chen, Rongchang
发表日期
2021-04-01
DOI
发表期刊
ISSN
2305-5839
EISSN
2305-5847
卷号9期号:8
摘要
["Background: Dysfunctional phenotype modulation and calcium channels in airway smooth muscle cells (ASMCs) are important characteristics of airway remodeling in chronic asthma. However, the mechanisms underlying these pathological processes remain unclear. SET (I2PP2A, inhibitor-2 of protein phosphatase 2A) has many significant functions and is involved in various physiological and pathological processes. This study aimed to determine the function of SET in chronic asthma.","Methods: BALB/c mice were sensitized by ovalbumin injection and repeated inhalation of ovalbumin. The Penh value was measured using the Buxco whole body plethysmography system. A short hairpin RNA of the SET gene was designed and transfected into ASMCs derived from asthmatic mice. Flow cytometry of Annexin-V/propidium iodide staining was used for evaluating cell apoptosis. Western blot was adopted to measure the expression levels of ASMCs phenotype modulation markers and calcium channel-associated proteins.","Results: The results showed that shRNA targeting SET significantly decreased the expression of SET, and enhanced the apoptosis of ASMCs. SET knockdown promoted the expression of contractile phenotype markers such as alpha-SMA (alpha smooth muscle Actin), SM-MHC (smooth muscle Myosin heavy chain), and calponin, and inhibited the expression of synthetic phenotype markers including vimentin and CD44. The expression of the calcium channel-related proteins STIM1 (Stromal interaction molecule 1) and Orai1 were also inhibited after SET knockdown.","Conclusions: These data demonstrated that SET participated in the development of airway dysfunction in asthma, suggesting that the silencing of SET may be a new therapeutic target for the treatment of asthma patients."]
关键词
相关链接[来源记录]
收录类别
语种
英语
学校署名
第一 ; 通讯
资助项目
NSFC[81770028]
WOS研究方向
Oncology ; Research & Experimental Medicine
WOS类目
Oncology ; Medicine, Research & Experimental
WOS记录号
WOS:000647716600011
出版者
来源库
Web of Science
引用统计
被引频次[WOS]:1
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/228395
专题南方科技大学第一附属医院
作者单位
Jinan Univ, Southern Univ Sci & Technol, Clin Med Coll 2,Shenzhen Inst Resp Dis, Affiliated Hosp 1,Shenzhen Peoples Hosp,Key Lab S, Shenzhen, Peoples R China
第一作者单位南方科技大学第一附属医院
通讯作者单位南方科技大学第一附属医院
第一作者的第一单位南方科技大学第一附属医院
推荐引用方式
GB/T 7714
Li, Jie,He, Qi,Wang, Lingwei,et al. SET knockdown attenuated phenotype modulation and calcium channel associated markers of airway smooth muscle cells in asthmatic mice[J]. Annals of Translational Medicine,2021,9(8).
APA
Li, Jie.,He, Qi.,Wang, Lingwei.,Chen, Dandan.,Qiu, Chen.,...&Chen, Rongchang.(2021).SET knockdown attenuated phenotype modulation and calcium channel associated markers of airway smooth muscle cells in asthmatic mice.Annals of Translational Medicine,9(8).
MLA
Li, Jie,et al."SET knockdown attenuated phenotype modulation and calcium channel associated markers of airway smooth muscle cells in asthmatic mice".Annals of Translational Medicine 9.8(2021).
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