Adamson I Y, Bowden D H
Am J Pathol. 1983 Aug;112(2):224-30.
Cytokinetic relationships between endothelial cells and fibroblasts during lung injury and repair in mice have been studied in a morphologic, autoradiographic, and biochemical study following whole body irradiation. After 650 rads, endothelial injury accompanied by interstitial edema was seen between weeks 1 and 2. The cell labeling curve had two components: predominant endothelial labeling to 3 weeks, then a smaller rise in DNA synthesis in interstitial cells. There was focal fibrosis but little change in total hydroxyproline to 20 weeks. After 1000 rads, cell injury, still confined to the endothelium, was more severe and lasted up to 6 weeks. Increased DNA synthesis occurred in the endothelium between Weeks 2 and 8 and in interstitial cells from Week 3 to 16, when total hydroxyproline was significantly elevated and many fibrotic areas were seen in the lung. The results indicate that acute endothelial injury may be rapidly repaired with little fibroblastic stimulation, whereas severe or prolonged injury with delayed regeneration disturbs endothelial-mesenchymal relationships. This may be a key factor in promoting fibroblast proliferation and the deposition of collagen.
在对小鼠进行全身照射后的一项形态学、放射自显影和生化研究中,对肺损伤和修复过程中内皮细胞与成纤维细胞之间的细胞动力学关系进行了研究。650拉德照射后,在第1周和第2周之间可见伴有间质性水肿的内皮损伤。细胞标记曲线有两个部分:内皮细胞标记在3周内占主导,然后间质细胞中的DNA合成有较小幅度的上升。有局灶性纤维化,但到20周时总羟脯氨酸变化不大。1000拉德照射后,细胞损伤仍局限于内皮细胞,更为严重且持续长达6周。第2周和第8周之间内皮细胞中DNA合成增加,第3周和第16周间质细胞中DNA合成增加,此时总羟脯氨酸显著升高,肺中可见许多纤维化区域。结果表明,急性内皮损伤可能在几乎没有成纤维细胞刺激的情况下迅速修复,而严重或长期损伤以及再生延迟会扰乱内皮-间充质关系。这可能是促进成纤维细胞增殖和胶原蛋白沉积的关键因素。