Mesenchymal stem cell-derived exosomes: a promising alternative in the therapy of preeclampsia

间充质干细胞 微泡 子痫前期 干细胞 医学 免疫系统 癌症研究 血管生成 免疫学 干细胞疗法 生物信息学 怀孕 生物 病理 小RNA 细胞生物学 生物化学 遗传学 基因
作者
Haoran Shi,Zejun Yang,Jianjian Cui,Hui Tao,Ruilin Ma,Yin Zhao
出处
期刊:Stem Cell Research & Therapy [BioMed Central]
卷期号:15 (1) 被引量:9
标识
DOI:10.1186/s13287-024-03652-0
摘要

Abstract Preeclampsia (PE) is a common morbid complication during pregnancy, affecting 2%-8% of pregnancies globally and posing serous risks to the health of both mother and fetus. Currently, the only effective treatment for PE is timely termination of pregnancy, which comes with increased perinatal risks. However, there is no effective way to delay pathological progress and improve maternal and fetal outcomes. In light of this, it is of great significance to seek effective therapeutic strategies for PE. Exosomes which are nanoparticles carrying bioactive substances such as proteins, lipids, and nucleic acids, have emerged as a novel vehicle for intercellular communication. Mesenchymal stem cell-derived exosomes (MSC-Exos) participate in various important physiological processes, including immune regulation, cell proliferation and migration, and angiogenesis, and have shown promising potential in tissue repair and disease treatment. Recently, MSC-Exos therapy has gained popularity in the treatment of ischaemic diseases, immune dysfunction, inflammatory diseases, and other fields due to their minimal immunogenicity, characteristics similar to donor cells, ease of storage, and low risk of tumor formation. This review elaborates on the potential therapeutic mechanism of MSC-Exos in treating preeclampsia, considering the main pathogenic factors of the condition, including placental vascular dysplasia, immunological disorders, and oxidative stress, based on the biological function of MSC-Exos. Additionally, we discuss in depth the advantages and challenges of MSC-Exos as a novel acellular therapeutic agent in preeclampsia treatment.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
聪明的哈密瓜完成签到,获得积分10
刚刚
liuyue完成签到,获得积分10
刚刚
Yuqi发布了新的文献求助10
1秒前
mxdckd完成签到,获得积分10
1秒前
天行马完成签到,获得积分10
2秒前
84完成签到,获得积分10
2秒前
独特的靖琪完成签到,获得积分10
2秒前
SVR发布了新的文献求助10
2秒前
筷子夹豆腐脑完成签到,获得积分10
3秒前
尹冰露发布了新的文献求助10
3秒前
JamesPei应助ten采纳,获得10
3秒前
levitt233完成签到,获得积分10
3秒前
郝不错完成签到,获得积分10
4秒前
nn完成签到,获得积分10
4秒前
wf完成签到,获得积分0
4秒前
暮寻屿苗完成签到 ,获得积分10
4秒前
哈库呐马塔塔完成签到,获得积分10
4秒前
4秒前
鳗鱼雪巧完成签到,获得积分10
4秒前
opticsLM完成签到,获得积分10
5秒前
心无杂念发布了新的文献求助10
6秒前
6秒前
Xingkun_li完成签到,获得积分10
6秒前
QIU完成签到 ,获得积分10
6秒前
shin0324完成签到,获得积分10
7秒前
开朗大雁完成签到,获得积分10
7秒前
闪闪的灵寒完成签到,获得积分10
7秒前
XF完成签到,获得积分10
7秒前
沙漏的回忆完成签到,获得积分10
7秒前
huan发布了新的文献求助10
9秒前
9秒前
内向灵凡完成签到,获得积分10
9秒前
幸福的小刺猬完成签到,获得积分10
9秒前
9秒前
罗霄山完成签到,获得积分10
9秒前
菠萝汁完成签到,获得积分10
9秒前
9秒前
Lucas应助Zz采纳,获得10
9秒前
chen完成签到,获得积分10
9秒前
木子林希儿完成签到,获得积分10
10秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Organometallic Chemistry of the Transition Metals 800
Chemistry and Physics of Carbon Volume 18 800
The Organometallic Chemistry of the Transition Metals 800
The formation of Australian attitudes towards China, 1918-1941 640
Signals, Systems, and Signal Processing 610
全相对论原子结构与含时波包动力学的理论研究--清华大学 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6441010
求助须知:如何正确求助?哪些是违规求助? 8254899
关于积分的说明 17573326
捐赠科研通 5499523
什么是DOI,文献DOI怎么找? 2900128
邀请新用户注册赠送积分活动 1876823
关于科研通互助平台的介绍 1716941