Therapeutic effects and potential mechanisms of endoscopic submucosal injection of mesenchymal stem cells on chronic atrophic gastritis

间充质干细胞 细胞凋亡 萎缩性胃炎 癌症研究 体内 病理 体外 医学 生物 免疫学 胃炎 内科学 生物化学 生物技术
作者
Qianqian Xu,Mingyue Liu,Rui Meng,Qi Zhao,Xiaoxiao Men,Yadi Lan,Hongwei Xu
出处
期刊:Scientific Reports [Nature Portfolio]
卷期号:13 (1) 被引量:5
标识
DOI:10.1038/s41598-023-48088-3
摘要

Abstract Previous studies have demonstrated the rejuvenating and restorative actions of mesenchymal stem cells (MSCs) in multiple diseases, but their role in reversing chronic atrophic gastritis (CAG) is not well understood owing to their low efficiency in homing to the stomach. In this work, we investigated the therapeutic effect of umbilical cord-derived MSCs (UC-MSCs) on CAG by endoscopic submucosal injection and preliminarily explored possible mechanisms in vitro. MSCs and normal saline (NS) were injected into the submucosa of the stomach in randomly grouped CAG rabbits. Therapeutic effects on serum indices and histopathology of the gastric mucosa were analyzed in vivo at 30 and 60 days after MSCs injection. GES-1 cells were co-cultured with MSCs in vitro using a Transwell system and cell viability, proliferation, and migration ability were detected. Additionally, in view of the potential mechanisms, the relative protein expression levels of apoptosis, autophagy and inflammation in vitro were explored by Western Blotting. We found that submucosal injection of MSCs up-regulated serum indices (G-17, PGI and PGI/PGII) and alleviated histopathological damage to the gastric mucosa in CAG rabbits. Co-culture of GES-1 cells with MSCs improved cell viability, proliferation, and migration ability, while suppressing apoptosis. We also observed a reduction in the expression of apoptosis indicators, including Bax and cleaved caspase-3, in GES-1 cells after co-culture with MSCs in vitro. Our findings suggest that submucosal injection of MSCs is a promising approach for reversing CAG, and attenuating apoptosis plays a potential role in this process.
最长约 10秒,即可获得该文献文件

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
1秒前
Keepsome完成签到,获得积分10
2秒前
饮了风发布了新的文献求助10
4秒前
4秒前
高丰完成签到,获得积分20
4秒前
5秒前
星矢一道完成签到 ,获得积分10
6秒前
迷你的书包完成签到,获得积分20
6秒前
6秒前
999发布了新的文献求助10
6秒前
6秒前
He完成签到 ,获得积分10
7秒前
Li发布了新的文献求助10
7秒前
7秒前
搜集达人应助悦耳语堂采纳,获得10
8秒前
阔达岂愈发布了新的文献求助10
9秒前
丘比特应助郝好采纳,获得10
9秒前
bingqian_yao发布了新的文献求助10
9秒前
9秒前
9秒前
吴晓曼发布了新的文献求助10
10秒前
10秒前
随机完成签到,获得积分10
11秒前
所所应助聪明的梦槐采纳,获得10
11秒前
12秒前
Owen应助科研通管家采纳,获得10
12秒前
Copyright应助科研通管家采纳,获得10
13秒前
小蘑菇应助科研通管家采纳,获得10
13秒前
梁海萍发布了新的文献求助10
13秒前
13秒前
小蘑菇应助nono采纳,获得10
13秒前
Ava应助科研通管家采纳,获得10
13秒前
无花果应助科研通管家采纳,获得10
13秒前
13秒前
13秒前
Ava应助科研通管家采纳,获得10
13秒前
小二郎应助科研通管家采纳,获得10
13秒前
烟花应助科研通管家采纳,获得10
14秒前
14秒前
柏柏应助科研通管家采纳,获得10
14秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
Molecular Mechanisms of Photosynthesis, 4th Edition 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
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 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7266469
求助须知:如何正确求助?哪些是违规求助? 8887485
关于积分的说明 18784709
捐赠科研通 6943701
什么是DOI,文献DOI怎么找? 3203143
关于科研通互助平台的介绍 2376131
邀请新用户注册赠送积分活动 2179039