Huang Xiaoping, Wang Xiao, Xie Xiaolan, Zeng Shulan, Li Zhaofa, Xu Xianxiang, Yang Huiyong, Qiu Fei, Lin Junsheng, Diao Yong
Institute of Molecular Medicine, Huaqiao UniversityQuanzhou 362021, China; College of Chemical Engineering and Materials Sciences, Quanzhou Normal UniversityQuanzhou 326000, China.
Institute of Molecular Medicine, Huaqiao University Quanzhou 362021, China.
Am J Transl Res. 2017 Mar 15;9(3):999-1011. eCollection 2017.
Aberrant angiogenesis and vascular remodeling are the main features of idiopathic pulmonary fibrosis. Kallistatin is an anti-angiogenic peptide with known effects on endothelial cells. This study aimed to demonstrate that kallistatin has beneficial effects on bleomycin (BLM)-induced pulmonary fibrosis in a rat model by inhibiting angiogenesis. Twenty-five rats were randomly divided into five experimental groups: (A) Saline only (SA)-as the negative control, (B) BLM only (BLM)-as the model group, (C) BLM and 0.1 mg/kg kallistatin (L-Kal), (D) BLM and 0.5 mg/kg kallistatin (M-Kal), and (E) BLM and 2.5 mg/kg kallistatin (H-Kal). Fibrillar collagen was quantified by Masson's trichrome and hematoxylin-eosin staining. Transforming growth factor-β1 (TGF-β1), α-smooth-muscle-actin (α-SMA) and microvascular density (MVD) were measured by immunohistochemistry. Vascular endothelial growth factor (VEGF), vascular endothelial growth factor receptor (VEGFR), and tumor necrosis factor-α (TNF-α) were assayed by Western immunoblotting or ELISA. Daily administration of kallistatin attenuated fibrosis in BLM-induced pulmonary fibrosis, as shown by histology. During inflammation from BLM-induced pulmonary fibrosis, kallistatin reduced the number of inflammatory cells infiltrating the bronchoalveolar lavage fluid. Kallistatin also inhibited VEGF expression and phosphorylation of VEGFR2 (Flk-1). In vitro, kallistatin blocked tube formation by inhibiting Flk-1 and GSK-3β phosphorylation. The results demonstrated that continuous administration of kallistatin attenuated BLM-induced pulmonary fibrosis and improved survival of BLM rats. Reducing pulmonary fibrosis was achieved by partial inhibition of pulmonary inflammation and angiogenesis.
异常血管生成和血管重塑是特发性肺纤维化的主要特征。激肽释放酶抑制蛋白是一种对内皮细胞有已知作用的抗血管生成肽。本研究旨在证明激肽释放酶抑制蛋白通过抑制血管生成对博来霉素(BLM)诱导的大鼠肺纤维化具有有益作用。25只大鼠随机分为五个实验组:(A)仅生理盐水(SA)——作为阴性对照,(B)仅博来霉素(BLM)——作为模型组,(C)博来霉素和0.1 mg/kg激肽释放酶抑制蛋白(L-Kal),(D)博来霉素和0.5 mg/kg激肽释放酶抑制蛋白(M-Kal),以及(E)博来霉素和2.5 mg/kg激肽释放酶抑制蛋白(H-Kal)。通过Masson三色染色和苏木精-伊红染色对纤维状胶原进行定量。通过免疫组织化学测量转化生长因子-β1(TGF-β1)、α-平滑肌肌动蛋白(α-SMA)和微血管密度(MVD)。通过Western免疫印迹或ELISA检测血管内皮生长因子(VEGF)、血管内皮生长因子受体(VEGFR)和肿瘤坏死因子-α(TNF-α)。组织学显示,每日给予激肽释放酶抑制蛋白可减轻BLM诱导的肺纤维化中的纤维化。在BLM诱导的肺纤维化炎症过程中,激肽释放酶抑制蛋白减少了支气管肺泡灌洗液中浸润的炎症细胞数量。激肽释放酶抑制蛋白还抑制VEGF表达和VEGFR2(Flk-1)的磷酸化。在体外,激肽释放酶抑制蛋白通过抑制Flk-1和GSK-3β磷酸化来阻断管腔形成。结果表明,持续给予激肽释放酶抑制蛋白可减轻BLM诱导的肺纤维化并提高BLM大鼠的存活率。通过部分抑制肺部炎症和血管生成实现了肺纤维化的减轻。