Kaarteenaho-Wiik R, Tani T, Sormunen R, Soini Y, Virtanen I, Pääkkö P
Department of Pathology, University of Oulu, Finland.
Am J Respir Crit Care Med. 1996 Aug;154(2 Pt 1):511-8. doi: 10.1164/ajrccm.154.2.8756830.
In this investigation, tenascin (Tn) expression was studied in 51 cases of different types of fibrotic lung disorders originating for years 1981 to 1995. Our aim was to test if accumulation of Tn at the site of lung injury in usual interstitial pneumonia (UIP) could correlate with the prognosis. Lung biopsies taken from 28 patients with UIP, six with desquamative interstitial pneumonia (DIP), six with sarcoidosis, five with extrinsic allergic bronchioloalveolitis, five with bronchiolitis obliterans organizing pneumonia (BOOP), and one with nonspecific interstitial pneumonia were studied for the expression of Tn by using an immunohistochemical technique. In addition to Tn immunohistochemistry, selected cases were also studied by immunoelectron microscopy and Western blotting. For prognostic studies in UIP the clinical follow-up information was obtained from the patient records. The expression of Tn was increased in each type of fibrosis, especially in UIP. In immunoelectron microscopy the most prominent labeling in UIP was found in association with collagen fibers and within the type 2 pneumocytes. Every studied case of UIP showed reactivity for a polypeptide of M(r) approximately equal to 200,000 by Western blotting. In patients with UIP, increased Tn expression, especially under metaplastic bronchiolar-type epithelium, was associated with a shortened survival time. Immunoelectron microscopic findings support the idea that Tn in UIP is synthesized by the regenerating epithelial rather than interstitial cells in response to pulmonary interstitial inflammation.
在本研究中,对1981年至1995年间51例不同类型的肺纤维化疾病患者的腱生蛋白(Tn)表达进行了研究。我们的目的是检验在寻常型间质性肺炎(UIP)的肺损伤部位Tn的积聚是否与预后相关。采用免疫组织化学技术,对28例UIP患者、6例脱屑性间质性肺炎(DIP)患者、6例结节病患者、5例外源性过敏性细支气管肺泡炎患者、5例闭塞性细支气管炎伴机化性肺炎(BOOP)患者及1例非特异性间质性肺炎患者的肺活检组织进行Tn表达研究。除了Tn免疫组织化学外,还对部分病例进行了免疫电子显微镜和蛋白质印迹分析。对于UIP的预后研究,从患者病历中获取临床随访信息。每种类型的纤维化中Tn表达均增加,尤其是在UIP中。免疫电子显微镜检查发现,UIP中最显著的标记与胶原纤维及Ⅱ型肺泡上皮细胞有关。通过蛋白质印迹分析,每个研究的UIP病例均显示对分子量约为200,000的多肽有反应。在UIP患者中,Tn表达增加,尤其是在化生的细支气管型上皮下,与生存时间缩短相关。免疫电子显微镜检查结果支持这样的观点,即UIP中的Tn是由再生的上皮细胞而非间质细胞合成,以应对肺间质炎症。