Cambrey A D, Harrison N K, Dawes K E, Southcott A M, Black C M, du Bois R M, Laurent G J, McAnulty R J
Department of Thoracic Medicine, National Heart and Lung Institute, London, United Kingdom.
Am J Respir Cell Mol Biol. 1994 Oct;11(4):439-45. doi: 10.1165/ajrcmb.11.4.7917311.
Pulmonary fibrosis is a major cause of morbidity and mortality in patients with systemic sclerosis (SSc). The pathogenesis of this condition is poorly understood, but one of the earliest pathologic features is endothelial and epithelial cell injury with subsequent regeneration. Endothelial and epithelial cells can release several mediators, including endothelin-1 (ET-1). In this study, we investigated the levels of ET-1 in bronchoalveolar lavage fluid (BALF) from patients with SSc and assessed the contribution of ET-1 to the fibroblast mitogenic activity induced by these fluids. A total of 26 patients were evaluated and divided into those with evidence of pulmonary fibrosis, assessed by thin-section computed tomography (group I, n = 16), and those with a normal scan (group II, n = 10). BALF from both groups of patients stimulated fibroblast proliferation. Values expressed as median (range) percentage increase above media controls were 25.5% (5.0 to 47.8%) and 27.6% (10.9 to 51.6%) for groups I and II, respectively (P < 0.02 in both cases). Mitogenic activity was inhibited by about 40% in the presence of either a neutralizing antibody to ET-1 or two synthetic ET-1 receptor ligands. Levels of ET-1 in BALF, expressed as medians (range) were 2.90 ng/mg albumin (0.68 to 5.75) in patients with SSc and 1.23 ng/mg albumin (0.84 to 2.0) in control patients (P < 0.02). Furthermore, ET-1 levels in BALF from patients in group II (3.83 ng/mg albumin, range 1.76 to 5.75) were elevated compared with those in group I (2.62 ng/mg albumin, range 0.68 to 3.81; P < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
肺纤维化是系统性硬化症(SSc)患者发病和死亡的主要原因。这种疾病的发病机制尚不清楚,但最早的病理特征之一是内皮细胞和上皮细胞损伤及随后的再生。内皮细胞和上皮细胞可释放多种介质,包括内皮素-1(ET-1)。在本研究中,我们调查了SSc患者支气管肺泡灌洗液(BALF)中ET-1的水平,并评估了ET-1对这些液体诱导的成纤维细胞有丝分裂活性的作用。共评估了26例患者,根据薄层计算机断层扫描分为有肺纤维化证据的患者(I组,n = 16)和扫描正常的患者(II组,n = 10)。两组患者的BALF均刺激成纤维细胞增殖。以高于培养基对照的中位数(范围)百分比增加表示的值,I组和II组分别为25.5%(5.0至47.8%)和27.6%(10.9至51.6%)(两种情况P均<0.02)。在存在ET-1中和抗体或两种合成ET-1受体配体的情况下,有丝分裂活性被抑制约40%。SSc患者BALF中ET-1水平以中位数(范围)表示为2.90 ng/mg白蛋白(0.68至5.75),对照患者为1.23 ng/mg白蛋白(0.84至2.0)(P<0.02)。此外,II组患者BALF中ET-1水平(3.83 ng/mg白蛋白,范围1.76至5.75)高于I组(2.62 ng/mg白蛋白,范围0.68至3.81;P<0.05)。(摘要截断于250字)