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Exosomes derived from smooth muscle cells ameliorate diabetes-induced erectile dysfunction by inhibiting fibrosis and modulating the NO/cGMP pathway

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单位: [1]Huazhong Univ Sci & Technol,Dept Urol,Tongji Hosp,Tongji Med Coll,Wuhan 430030,Hubei,Peoples R China [2]Huazhong Univ Sci & Technol,Inst Urol,Tongji Hosp,Tongji Med Coll,Wuhan 430030,Hubei,Peoples R China
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关键词: diabetes erectile dysfunction exosomes fibrosis NO cGMP signalling pathway

摘要:
Erectile dysfunction (ED) is a major health issue among men with diabetes, and ED induced by diabetes mellitus (DMED) is particularly difficult to treat. Therefore, novel therapeutic approaches for the treatment of DMED are urgently needed. Exosomes, nanosized particles involved in many physiological and pathological processes, may become a promising tool for DMED treatment. In this study, we investigated the therapeutic effect of exosomes derived from corpus cavernosum smooth muscle cells (CCSMC-EXOs) on erectile function in a rat model of diabetes and compared their effect with that of exosomes derived from mesenchymal stem cells (MSC-EXOs). We incubated labelled CCSMC-EXOs and MSC-EXOs with CCSMCs and then observed uptake of the exosomes at different time points using laser confocal microscopy. CCSMC-EXOs were more easily taken up by CCSMCs. The peak concentration and retention time of labelled CCSMC-EXOs and MSC-EXOs in the corpus cavernosum of DMED rats after intracavernous injection were compared by in vivo imaging techniques. Intracavernous injection of CCSMC-EXOs was associated with a relatively high peak concentration and long retention time. Our data showed that CCSMC-EXOs could improve erectile function in DMED rats. Meanwhile, CCSMC-EXOs could exert antifibrotic effects by increasing the smooth muscle content and reducing collagen deposition. CCSMC-EXOs also increased the expression of eNOS and nNOS, followed by increased levels of NO and cGMP. These findings initially identify the possible role of CCSMC-EXOs in ameliorating DMED through inhibiting corporal fibrosis and modulating the NO/cGMP signalling pathway, providing a theoretical basis for a breakthrough in the treatment of DMED.

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出版当年[2019]版:
大类 | 2 区 医学
小类 | 2 区 医学:研究与实验 3 区 细胞生物学
最新[2025]版:
大类 | 3 区 医学
小类 | 3 区 细胞生物学 3 区 医学:研究与实验
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出版当年[2018]版:
Q1 MEDICINE, RESEARCH & EXPERIMENTAL Q2 CELL BIOLOGY
最新[2024]版:
Q2 CELL BIOLOGY Q2 MEDICINE, RESEARCH & EXPERIMENTAL

影响因子: 最新[2024版] 最新五年平均 出版当年[2018版] 出版当年五年平均 出版前一年[2017版] 出版后一年[2019版]

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第一作者单位: [1]Huazhong Univ Sci & Technol,Dept Urol,Tongji Hosp,Tongji Med Coll,Wuhan 430030,Hubei,Peoples R China [2]Huazhong Univ Sci & Technol,Inst Urol,Tongji Hosp,Tongji Med Coll,Wuhan 430030,Hubei,Peoples R China
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通讯机构: [1]Huazhong Univ Sci & Technol,Dept Urol,Tongji Hosp,Tongji Med Coll,Wuhan 430030,Hubei,Peoples R China [2]Huazhong Univ Sci & Technol,Inst Urol,Tongji Hosp,Tongji Med Coll,Wuhan 430030,Hubei,Peoples R China
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