Gong Limin, Du Junbao, Zhao Weihong, Tian Hong, Tang Chaoshu
Department of Pediatrics, Peking University First Hospital, Beijing 100034 China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2003 Dec 18;35(6):571-5.
To explore changes of expression of heme oxygenase (HO) and production of endogenous carbon monoxide in hypoxic pulmonary artery smooth muscle cells (PASMCs) of rats and study their effects on type I collagen under hypoxia.
PASMCs of rats were cultured in vitro and incubated under hypoxic condition for 24 hours. The relative content of CO released into medium by PASMCs was detected using spectrophotometry. Western blot was applied to assay the expressions of HO-1 and transforming growth factor-beta(3) (TGF-beta(3)). The expressions of HO-1, TGF-beta(3) and type I collagen were detected by immunohistochemical assay. The expressions of procollagen type I were detected by in situ hybridization.
Hypoxia induced the expression of TGF-beta(3), type I collagen and mRNA in rat PASMCs, elevated the expression of HO-1 and CO content compared to controls by 67.45% (P<0.01) and 35.41% (P<0.05), respectively. In the hypoxic PASMCs treated with protoporphyrin-IX (ZnPP)(10 micromol x L(-1)), an inhibitor of HO, the expression of HO-1 and the CO content were 23.9%(P<0.05), 7.88% (P<0.01) lower than those of hypoxic PASMCs, respectively. ZnPP promoted the expression of TGF-beta(3) (393%,P<0.01), type I collagen protein and mRNA in hypoxic PASMCs. Hemin (20 micromol x L(-1)), an inducer of HO, caused an increase in the expression of HO-1 and CO content in hypoxic rat PASMCs by 105% (P<0.05), 8.83% (P<0.01) compared to hypoxic PASMCs, respectively. Hemin inhibited the expression of TGF-beta(3) by 68.12% (P<0.01), and type I collagen protein and mRNA in hypoxic PASMCs.
HO/CO system is up-regulated by hypoxia and endogenous CO may play an important role in decreasing collagen synthesis and inhibiting the expression of TGF-beta(3) in hypoxic rat PASMCs.
探讨大鼠缺氧性肺动脉平滑肌细胞(PASMCs)中血红素加氧酶(HO)表达及内源性一氧化碳生成的变化,并研究其在缺氧状态下对Ⅰ型胶原蛋白的影响。
体外培养大鼠PASMCs,并在缺氧条件下孵育24小时。采用分光光度法检测PASMCs释放到培养基中的CO相对含量。应用蛋白质免疫印迹法检测HO-1和转化生长因子-β3(TGF-β3)的表达。采用免疫组织化学法检测HO-1、TGF-β3和Ⅰ型胶原蛋白的表达。采用原位杂交法检测Ⅰ型前胶原的表达。
缺氧诱导大鼠PASMCs中TGF-β3、Ⅰ型胶原蛋白及其mRNA表达,与对照组相比,HO-1表达及CO含量分别升高67.45%(P<0.01)和35.41%(P<0.05)。用HO抑制剂原卟啉-IX(ZnPP,10 μmol·L⁻¹)处理缺氧的PASMCs后,HO-1表达及CO含量分别比缺氧PASMCs降低23.9%(P<0.05)、7.88%(P<0.01)。ZnPP促进缺氧PASMCs中TGF-β3表达(393%,P<0.01)、Ⅰ型胶原蛋白蛋白及其mRNA表达。HO诱导剂血红素(20 μmol·L⁻¹)使缺氧大鼠PASMCs中HO-1表达及CO含量分别比缺氧PASMCs增加105%(P<0.05)、8.83%(P<0.01)。血红素使缺氧PASMCs中TGF-β3表达降低68.12%(P<0.01)、Ⅰ型胶原蛋白蛋白及其mRNA表达降低。
缺氧上调HO/CO系统,内源性CO可能在降低缺氧大鼠PASMCs中胶原蛋白合成及抑制TGF-β3表达方面发挥重要作用。