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人脐带间充质干细胞与FTY720联合治疗减轻小鼠模型中脂多糖诱导的急性肺损伤。

Combination therapy of human umbilical cord mesenchymal stem cells and FTY720 attenuates acute lung injury induced by lipopolysaccharide in a murine model.

作者信息

Zhang Zili, Li Wenfei, Heng Zhizhi, Zheng Jing, Li Puyuan, Yuan Xin, Niu Wenkai, Bai Changqing, Liu Huiying

机构信息

Department of Respiratory and Critical Care Diseases, 307th Hospital of PLA, Beijing 100071, China.

Anhui Medical University, Hefei 230032, China.

出版信息

Oncotarget. 2017 Aug 24;8(44):77407-77414. doi: 10.18632/oncotarget.20491. eCollection 2017 Sep 29.

DOI:10.18632/oncotarget.20491
PMID:29100396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5652788/
Abstract

ALI/ARDS remain the main reason of morbidity and mortality in the critically ill. Studies have indicated that human umbilical cord mesenchymal stem cells (hUC-MSCs) can be useful in the treatment of ALI/ARDS. Sphingosine-1-phosphate (S1P) and its analog FTY720 significantly reduce lipopolysaccharide (LPS)-induced lung edema and inflammatory lung injury. This study aimed to assess the therapeutic effects of hUC-MSCs combined with FTY720 in an LPS-induced murine model of ALI. Eight-week-old female C57BL/6 mice were divided into a normal control group, an LPS group, an hUC-MSC group, an FTY720 group, and an hUC-MSCs+FTY720 group randomly. At 24 hours post injury, mice were administrated hUC-MSCs via the tail vein and/or intraperitoneally injected with FTY720. We assessed histopathology and histologic scores, lung wet/dry weight ratio, micro-CT scans, and total protein in the bronchoalveolar lavage fluid (BALF), as well as cytokines in the BALF at 48 h post injury. All treatment groups showed higher survival rates and attenuated lung injuries. The hUC-MSCs+FTY720 group yielded better results than hUC-MSCs or FTY720 alone. While the underlying mechanism requires further study, we anticipate that combination therapy of hUC-MSCs and FTY720 could be an effective strategy for ALI.

摘要

急性肺损伤/急性呼吸窘迫综合征(ALI/ARDS)仍然是危重症患者发病和死亡的主要原因。研究表明,人脐带间充质干细胞(hUC-MSCs)可用于治疗ALI/ARDS。鞘氨醇-1-磷酸(S1P)及其类似物FTY720可显著减轻脂多糖(LPS)诱导的肺水肿和肺部炎性损伤。本研究旨在评估hUC-MSCs联合FTY720在LPS诱导的ALI小鼠模型中的治疗效果。将8周龄雌性C57BL/6小鼠随机分为正常对照组、LPS组、hUC-MSC组、FTY720组和hUC-MSCs+FTY720组。在损伤后24小时,经尾静脉给小鼠输注hUC-MSCs和/或腹腔注射FTY720。我们在损伤后48小时评估了组织病理学和组织学评分、肺湿/干重比、微型计算机断层扫描(micro-CT)以及支气管肺泡灌洗液(BALF)中的总蛋白,以及BALF中的细胞因子。所有治疗组均显示出较高的存活率和减轻的肺损伤。hUC-MSCs+FTY720组的效果优于单独使用hUC-MSCs或FTY720组。虽然其潜在机制需要进一步研究,但我们预计hUC-MSCs与FTY72联合治疗可能是治疗ALI的有效策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/5652788/162e2ff66352/oncotarget-08-77407-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/5652788/76123c4f4057/oncotarget-08-77407-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/5652788/162e2ff66352/oncotarget-08-77407-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/5652788/76123c4f4057/oncotarget-08-77407-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/5652788/88dd7f7efd1b/oncotarget-08-77407-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/5652788/646a77c5658d/oncotarget-08-77407-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/5652788/5053513e2ef1/oncotarget-08-77407-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/5652788/13e12390cd53/oncotarget-08-77407-g005.jpg
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