Suzuki N, Ohta K, Horiuchi T, Takizawa H, Ueda T, Kuwabara M, Shiga J, Ito K
Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo, Japan.
Thorax. 1996 Oct;51(10):1036-42. doi: 10.1136/thx.51.10.1036.
Silica-induced pulmonary inflammation and fibrosis in animals provides a good model for chronic pulmonary inflammation and fibrosis. Although lymphocytes are implicated in the pathogenesis of pulmonary fibrosis, experimental models using silica-treated athymic nude mice have not been successful in showing the fibrogenic mechanism regulated by T cells. The aim of this study was to re-evaluate the role of T lymphocytes in the development of silicosis by comparing the response to silica administration of nude athymic mutants with that of euthymic animals.
Suspensions of silica particles were transnasally administered to nude athymic mice (Balb/c nu/nu) as well as to their euthymic littermates (Balb/c nu/+). The degree of pulmonary inflammation and fibrosis was assessed on days 14, 28, and 56 based upon histological observation, analysis of collagen deposition in the lungs, and analysis of the cellular constituent, protein, and phospholipid content in the bronchoalveolar lavage fluid.
Histologically, athymic mice developed less severe interstitial pneumonitis than euthymic mice. In euthymic mice the lung hydroxyproline content increased with time after silica administration from 6.48 (0.38) micrograms hydroxyproline/mg dry lung weight on day 0 to 8.87 (0.41) micrograms/mg on day 56. A gradual increase in lung hydroxyproline content was also observed in athymic mice but the increase was significantly smaller than in euthymic mice (6.63 (0.43) micrograms/mg on day 0, 7.90 (0.19) micrograms/mg on day 56). Administration of silica resulted in an increase in the number of macrophages and neutrophils and in the total protein and phospholipid content of the bronchoalveolar lavage (BAL) fluid in both mouse strains. No significant difference was detected between athymic and euthymic mice in the numbers of macrophages, but the increase in neutrophils in the BAL fluid of athymic mice was significantly smaller than in euthymic mice on days 14 and 56. The total protein and phospholipid content of the BAL fluid from athymic mice was lower than that from euthymic mice.
T lymphocytes appear to be involved in the pathogenesis of silica-induced pneumonitis. Since pulmonary fibrosis develops even in nude athymic mice, T cells do not seem to play a primary part in fibrogenic response but they regulate, at least to some extent, the response of inflammatory cells and fibrogenesis of the lung.
二氧化硅诱导的动物肺部炎症和纤维化是慢性肺部炎症和纤维化的良好模型。尽管淋巴细胞与肺纤维化的发病机制有关,但使用经二氧化硅处理的无胸腺裸鼠的实验模型未能成功显示由T细胞调节的纤维化机制。本研究的目的是通过比较无胸腺裸鼠突变体和有胸腺动物对二氧化硅给药的反应,重新评估T淋巴细胞在矽肺发展中的作用。
将二氧化硅颗粒悬浮液经鼻给予无胸腺裸鼠(Balb/c nu/nu)及其有胸腺的同窝小鼠(Balb/c nu/+)。在第14、28和56天,根据组织学观察、肺中胶原沉积分析以及支气管肺泡灌洗液中细胞成分、蛋白质和磷脂含量分析,评估肺部炎症和纤维化程度。
组织学上,无胸腺小鼠发生的间质性肺炎比有胸腺小鼠轻。在有胸腺小鼠中,二氧化硅给药后肺羟脯氨酸含量随时间增加,从第0天的6.48(0.38)微克羟脯氨酸/毫克干肺重增加到第56天的8.87(0.41)微克/毫克。在无胸腺小鼠中也观察到肺羟脯氨酸含量逐渐增加,但增加幅度明显小于有胸腺小鼠(第0天为6.63(0.43)微克/毫克,第56天为7.90(0.19)微克/毫克)。二氧化硅给药导致两种小鼠品系的巨噬细胞和中性粒细胞数量增加,以及支气管肺泡灌洗(BAL)液中总蛋白和磷脂含量增加。在巨噬细胞数量上,无胸腺小鼠和有胸腺小鼠之间未检测到显著差异,但在第14天和第56天,无胸腺小鼠BAL液中中性粒细胞的增加明显小于有胸腺小鼠。无胸腺小鼠BAL液中的总蛋白和磷脂含量低于有胸腺小鼠。
T淋巴细胞似乎参与了二氧化硅诱导的肺炎的发病机制。由于即使在无胸腺裸鼠中也会发生肺纤维化,T细胞似乎在纤维化反应中不发挥主要作用,但它们至少在一定程度上调节炎症细胞的反应和肺的纤维化形成。