Roncalli M, Springall D R, Maggioni M, Moradoghli-Haftvani A, Winter R J, Zhao L, Coggi G, Polak J M
Department of Histochemistry and Respiratory Medicine, Royal Postgraduate Medical School, London, United Kingdom.
Am J Respir Cell Mol Biol. 1993 Nov;9(5):467-74. doi: 10.1165/ajrcmb/9.5.467.
Morphologic changes are reported to occur in rat lung vasculature after 3 days of hypoxia. We have previously shown that immunoreactivity for the vasodilator calcitonin gene-related peptide (CGRP) is increased in pulmonary endocrine cells by 7 days of hypoxia. Because these cells may be among the earliest mediators of the hypoxic response, we examined endocrine cell CGRP content in rat lung after 0, 2, 4, and 8 h and 1, 5, 10, 15, 20, 28, and 35 days of normobaric hypoxia, using optimal and supraoptimal dilutions of CGRP antibodies to demonstrate changes in CGRP immunoreactivity. This was compared with temporal changes in pulmonary vascular smooth muscle after 1, 5, and 20 days of hypoxia exposure by evaluating vascular immunoreactivity for alpha-smooth muscle actin (alpha-SM actin), platelet-derived growth factor (PDGF) beta-receptor, and proliferating cell nuclear antigen (PCNA). Significant increases in endocrine cell CGRP immunoreactivity were found after 4 h of hypoxia, and levels increased up to 1 day, followed by a decrease (at 5 days) and then a progressive increase up to 35 days. After 1 day of hypoxia, the number of vessels displaying immunoreactivity for alpha-SM actin, PDGF beta-receptor, and PCNA were also significantly increased. Whereas PDGF beta-receptor and PCNA returned to control values by day 20, alpha-SM actin reached a plateau that persisted until 20 days. The results indicate that modulation of endocrine cell CGRP content in response to hypoxia is rapid and characterized by a significant and persistent increase, paralleled by a proliferation of vascular cells leading to vascular muscularization.(ABSTRACT TRUNCATED AT 250 WORDS)
据报道,缺氧3天后大鼠肺血管系统会发生形态学变化。我们之前已经表明,缺氧7天后,肺内分泌细胞中血管舒张肽降钙素基因相关肽(CGRP)的免疫反应性会增加。由于这些细胞可能是缺氧反应的最早介质之一,我们使用CGRP抗体的最佳和超最佳稀释度来检测常压缺氧0、2、4和8小时以及1、5、10、15、20、28和35天后大鼠肺内分泌细胞CGRP含量,以证明CGRP免疫反应性的变化。通过评估α-平滑肌肌动蛋白(α-SM肌动蛋白)、血小板衍生生长因子(PDGF)β受体和增殖细胞核抗原(PCNA)的血管免疫反应性,将其与缺氧暴露1、5和20天后肺血管平滑肌的时间变化进行比较。缺氧4小时后,内分泌细胞CGRP免疫反应性显著增加,水平在1天内升高,随后下降(5天时),然后逐渐增加直至35天。缺氧1天后,显示α-SM肌动蛋白、PDGFβ受体和PCNA免疫反应性的血管数量也显著增加。虽然PDGFβ受体和PCNA在第20天时恢复到对照值,但α-SM肌动蛋白达到一个平台期并持续到20天。结果表明,对缺氧的反应中,内分泌细胞CGRP含量的调节迅速,其特征是显著且持续增加,同时血管细胞增殖导致血管肌化。(摘要截短于250字)