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气管抽吸间充质基质细胞的分离预测支气管肺发育不良。

Isolation of tracheal aspirate mesenchymal stromal cells predicts bronchopulmonary dysplasia.

机构信息

Department of Pediatrics and Communicable Diseases, University of Michigan Medical School, MSRBII, 1150 W Medical Center Dr, Ann Arbor, MI 48109-5688, USA.

出版信息

Pediatrics. 2010 Nov;126(5):e1127-33. doi: 10.1542/peds.2009-3445. Epub 2010 Oct 11.

Abstract

BACKGROUND

We have isolated mesenchymal stem cells (MSCs) from tracheal aspirates of premature infants with respiratory distress. Under the influence of transforming growth factor β, MSCs differentiate into α-smooth-muscle actin-expressing myofibroblasts. Myofibroblasts are increased in the lungs of patients with bronchopulmonary dysplasia (BPD), a chronic lung disease of prematurely born infants.

OBJECTIVE

We tested whether isolation of MSCs from tracheal aspirates of premature infants with respiratory distress during the first week of life correlates with BPD.

METHODS

Eighty-four infants born at a gestational age of <33 weeks and requiring mechanical ventilation were studied. Aspirates were collected during suctioning and centrifuged. Cell pellets were resuspended in culture medium and plated. Adherent cells were grown to confluence.

RESULTS

MSCs were isolated from the tracheal aspirates of 56 infants; 28 aspirate samples showed no MSCs. There was no statistical difference in gestational age or birth weight between the MSC and no-MSC groups. In the MSC group, 12 infants died and 25 developed BPD, as defined by a requirement for supplemental oxygen at 36 weeks' postmenstrual age. In the no-MSC group, 6 infants died and 1 developed BPD. Accounting for potential influences of gender, birth weight, gestational age, number of tracheal aspirate samples taken, and the duration of endotracheal intubation (up to 7 days), isolation of MSCs increased the adjusted odds ratio of BPD more than 21-fold (95% confidence interval: 1.82-265.85).

CONCLUSIONS

Isolation of tracheal aspirate MSCs predicts the development of BPD, which suggests that MSCs play an important role in the pathogenesis of this disease.

摘要

背景

我们已经从患有呼吸窘迫的早产儿的气管吸出物中分离出间充质干细胞(MSCs)。在转化生长因子β的影响下,MSCs 分化为表达α-平滑肌肌动蛋白的肌成纤维细胞。肌成纤维细胞在患有支气管肺发育不良(BPD)的患者的肺部中增加,BPD 是一种早产儿的慢性肺部疾病。

目的

我们测试了从患有呼吸窘迫的早产儿的气管吸出物中分离出 MSCs 是否与 BPD 相关。

方法

对 84 名胎龄小于 33 周且需要机械通气的婴儿进行了研究。在吸痰时收集吸出物并离心。细胞沉淀重悬于培养基中并接种。贴壁细胞生长至汇合。

结果

从 56 名婴儿的气管吸出物中分离出 MSCs;28 个吸出物样本中未发现 MSCs。MSC 组和无 MSC 组在胎龄或出生体重方面无统计学差异。在 MSC 组中,12 名婴儿死亡,25 名婴儿发展为 BPD,定义为在出生后 36 周需要补充氧气。在无 MSC 组中,6 名婴儿死亡,1 名婴儿发展为 BPD。考虑到性别、出生体重、胎龄、气管吸出物样本数量以及气管插管持续时间(长达 7 天)的潜在影响,分离 MSC 使 BPD 的调整后的优势比增加了 21 倍以上(95%置信区间:1.82-265.85)。

结论

分离气管吸出物 MSCs 预测 BPD 的发生,这表明 MSCs 在该疾病的发病机制中发挥重要作用。

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