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气管内移植人脐带血源间充质干细胞可减轻大肠杆菌诱导的小鼠急性肺损伤。

Intratracheal transplantation of human umbilical cord blood-derived mesenchymal stem cells attenuates Escherichia coli-induced acute lung injury in mice.

机构信息

Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Respir Res. 2011 Aug 15;12(1):108. doi: 10.1186/1465-9921-12-108.

Abstract

BACKGROUND

Human umbilical cord blood (UCB)-derived mesenchymal stem cells (MSCs) attenuate hyperoxic neonatal lung injury primarily through anti-inflammatory effects. We hypothesized that intratracheal transplantation of human UCB-derived MSCs could attenuate Escherichia coli (E. coli)-induced acute lung injury (ALI) in mice by suppressing the inflammatory response.

METHODS

Eight-week-old male ICR mice were randomized to control or ALI groups. ALI was induced by intratracheal E. coli instillation. Three-hours after E. coli instillation, MSCs, fibroblasts or phosphate-buffered saline were intratracheally administered randomly and survival was analyzed for 7 days post-injury. Lung histology including injury scores, myeloperoxidase (MPO) activity, and protein levels of interleukin (IL)-1α, IL-1β, IL-6, tumor necrosis factor (TNF)-α, and macrophage inflammatory protein (MIP)-2 as well as the wet-dry lung ratio and bacterial counts from blood and bronchoalveolar lavage (BAL) were evaluated at 1, 3, and 7 days post-injury. Levels of inflammatory cytokines in the lung were also profiled using protein macroarrays at day 3 post-injury which showed peak inflammation.

RESULTS

MSC transplantation increased survival and attenuated lung injuries in ALI mice, as evidenced by decreased injury scores on day 3 post-injury and reduced lung inflammation including increased MPO activity and protein levels of IL-1α, IL-1β, IL-6, TNF-α, and MIP-2 on day 3 and 7 post-injury. Inflammatory cytokine profiles in the lungs at day 3 post-injury were attenuated by MSC transplantation. MSCs also reduced the elevated lung water content at day 3 post-injury and bacterial counts in blood and BAL on day 7 post-injury.

CONCLUSIONS

Intratracheal transplantation of UCB-derived MSCs attenuates E. coli-induced ALI primarily by down-modulating the inflammatory process and enhancing bacterial clearance.

摘要

背景

人脐血(UCB)衍生的间充质干细胞(MSCs)通过抗炎作用减轻新生鼠高氧肺损伤。我们假设,通过抑制炎症反应,气管内移植人 UCB 衍生的 MSCs 可减轻大肠杆菌(E. coli)诱导的急性肺损伤(ALI)。

方法

将 8 周龄雄性 ICR 小鼠随机分为对照组或 ALI 组。通过气管内大肠杆菌滴注诱导 ALI。大肠杆菌滴注后 3 小时,随机给予 MSCs、成纤维细胞或磷酸盐缓冲盐水,分析损伤后 7 天的存活率。在损伤后 1、3 和 7 天,评估肺组织学,包括损伤评分、髓过氧化物酶(MPO)活性、白细胞介素(IL)-1α、IL-1β、IL-6、肿瘤坏死因子(TNF)-α和巨噬细胞炎症蛋白(MIP)-2 的蛋白水平,以及肺湿干重比和血液及支气管肺泡灌洗液(BAL)中的细菌计数。在损伤后 3 天,使用蛋白质宏阵列分析肺部炎症细胞因子水平,显示出炎症的高峰。

结果

MSC 移植可增加 ALI 小鼠的存活率并减轻肺损伤,表现在损伤后 3 天的损伤评分降低,以及肺炎症减轻,包括 MPO 活性和 IL-1α、IL-1β、IL-6、TNF-α和 MIP-2 的蛋白水平在损伤后 3 天和 7 天升高。损伤后 3 天,MSC 移植可减轻肺部炎症细胞因子谱。MSC 还可降低损伤后 3 天的肺含水量升高,并降低损伤后 7 天的血液和 BAL 中的细菌计数。

结论

气管内移植 UCB 衍生的 MSCs 主要通过下调炎症过程和增强细菌清除来减轻大肠杆菌诱导的 ALI。

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