Department of Pediatrics, General Hospital of Central Theater Command of Chinese People's Liberation Army, Wuhan, China.
Balkan Med J. 2022 Mar 14;39(1):130-139. doi: 10.4274/balkanmedj.galenos.2021.2021-9-8.
Acute respiratory distress syndrome (ARDS) is a severe disorder that is related to a high mortality. Mesenchymal stem cells (MSCs) have shown strong effects in relieving lung injury.
To determine the role of umbilical cord-derived MSCs (UC-MSCs) together with surfactant protein B (SP-B) in ARDS.
Animal experimentation.
Immunophenotypic characteristics of UC-MSCs were identified. BALB/c mice were intratracheally administrated with lipopolysaccharide (LPS) and received UC-MSCs or UC-MSCs transfected with SP-B (UC-MSCs-SP-B). Pathological changes and lung injury degrees after transplantation were assessed by histological and biochemical analyses. Inflammatory chemokine and cytokine production in the bronchoalveolar lavage fluid (BALF) was measured using enzyme-linked immunoassay. Flow cytometry was used to examine macrophage phenotypes and differentiation of T-helper 17 (Th17) and T-regulatory (Treg) in the BALF.
Our results showed that isolated UC-MSCs possessed multilineage differentiation potential. SP-B transfection into UC-MSCs strengthened the effects of UC-MSCs on lung function repair in LPS-induced ARDS. UC-MSCs and UC-MSCs-SP-B attenuated cellular infiltration. Additionally, UC-MSCs and UC-MSCs-SP-B inhibited the inflammatory response by promoting M2-like polarization, as well as reduced Th17 differentiation and promoted Treg differentiation.
UC-MSCs in combination with SP-B, alleviates inflammatory reaction in ARDS by regulating macrophage polarization.
急性呼吸窘迫综合征(ARDS)是一种严重的疾病,死亡率较高。间充质干细胞(MSCs)在缓解肺损伤方面显示出强大的作用。
确定脐带间充质干细胞(UC-MSCs)与表面活性蛋白 B(SP-B)联合在 ARDS 中的作用。
动物实验。
鉴定 UC-MSCs 的免疫表型特征。用脂多糖(LPS)气管内滴注 BALB/c 小鼠,并给予 UC-MSCs 或转染 SP-B 的 UC-MSCs(UC-MSCs-SP-B)。通过组织学和生化分析评估移植后病理变化和肺损伤程度。酶联免疫吸附试验测定支气管肺泡灌洗液(BALF)中炎症趋化因子和细胞因子的产生。流式细胞术检测 BALF 中巨噬细胞表型和 T 辅助 17(Th17)和 T 调节(Treg)的分化。
我们的结果表明,分离的 UC-MSCs 具有多能分化潜能。SP-B 转染到 UC-MSCs 中增强了 UC-MSCs 在 LPS 诱导的 ARDS 中对肺功能修复的作用。UC-MSCs 和 UC-MSCs-SP-B 减轻了细胞浸润。此外,UC-MSCs 和 UC-MSCs-SP-B 通过促进 M2 样极化来抑制炎症反应,减少 Th17 分化,促进 Treg 分化。
UC-MSCs 与 SP-B 联合应用通过调节巨噬细胞极化减轻 ARDS 中的炎症反应。