Department of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Tissue Eng Part A. 2012 Nov;18(21-22):2259-67. doi: 10.1089/ten.TEA.2011.0634. Epub 2012 Sep 24.
Bone marrow-derived mesenchymal stem cells (BM-MSC) can be differentiated into lung epithelial-like cells (MSC-EC) in vitro. The response of BM-MSC and MSC-EC to stimuli may vary because of their character and differentiation. We aimed to investigate the factors that may influence in vitro differentiation of BM-MSC to MSC-EC. We determined the response of BM-MSC, MSC-EC, bronchial epithelial cells, and alveolar epithelial cells to tumor necrosis factor (TNF)-α stimulation. We also investigated the changes in micro(mi)RNA-146a, miRNA-155, and TNF receptor 1 (TNFR1) expression after stimulation. Our results demonstrate that the addition of transforming growth factor-β(1) and extracellular matrix collagen are required to facilitate such differentiation. After 3 weeks of culture, the morphological appearance and expression of airway epithelial markers, cytokeratin and Clara cell secretory protein, in MSC-EC were characteristics of lung epithelial cells. In response to TNF-α stimulation, the maximal interleukin (IL)-8 production by BM-MSC at the 24-h time point was 4.8 times greater compared with MSC-EC. TNF-α induced a significant increase in the expression of miRNA-146a in BM-MSC as compared with MSC-EC. miRNA-155 expression remained unchanged after stimulation. TNFR1 mRNA also significantly increased in BM-MSC after TNF-α stimulation. This was not observed in MSC-EC. Transfection with miRNA-146a mimics resulted in a significant increase of miRNA-146a expression and IL-8 production in both types of cells. In contrast, miRNA-146a inhibitors reduced miRNA-146a expression and IL-8 production. Overexpression of miRNA-146a, which positively regulates TNF-α-induced IL-8 release, may enhance the inflammatory response in both BM-MSC and MSC-EC. The expression of miRNA-146a and the response to stimuli may be modulated through mature differentiation of BM-MSC.
骨髓间充质干细胞(BM-MSC)可在体外分化为肺上皮样细胞(MSC-EC)。由于其特性和分化,BM-MSC 和 MSC-EC 对刺激的反应可能会有所不同。我们旨在研究可能影响 BM-MSC 体外向 MSC-EC 分化的因素。我们测定了 BM-MSC、MSC-EC、支气管上皮细胞和肺泡上皮细胞对肿瘤坏死因子(TNF)-α刺激的反应。我们还研究了刺激后 micro(mi)RNA-146a、miRNA-155 和 TNF 受体 1(TNFR1)表达的变化。结果表明,需要添加转化生长因子-β(1)和细胞外基质胶原来促进这种分化。培养 3 周后,MSC-EC 中气道上皮标志物角蛋白和 Clara 细胞分泌蛋白的形态和表达特征为肺上皮细胞。在 TNF-α刺激下,24 小时时 BM-MSC 产生的最大白细胞介素(IL)-8 比 MSC-EC 多 4.8 倍。与 MSC-EC 相比,TNF-α诱导 BM-MSC 中 miRNA-146a 的表达显著增加。刺激后 miRNA-155 的表达保持不变。TNF-α刺激后,BM-MSC 中 TNFR1mRNA 也显著增加。在 MSC-EC 中未观察到这种情况。转染 miRNA-146a 模拟物可导致两种细胞中 miRNA-146a 的表达和 IL-8 的产生显著增加。相反,miRNA-146a 抑制剂降低了 miRNA-146a 的表达和 IL-8 的产生。miRNA-146a 的过表达正向调节 TNF-α诱导的 IL-8 释放,可能增强 BM-MSC 和 MSC-EC 中的炎症反应。miRNA-146a 的表达和对刺激的反应可能通过 BM-MSC 的成熟分化来调节。