Schneeberger E E, DeFerrari M, Skoskiewicz M J, Russell P S, Colvin R B
Lab Invest. 1986 Aug;55(2):138-44.
Recombinant murine interferon-gamma (IFN-gamma) was administered in 6 to 9 daily intraperitoneal injections to B10.BR (H-2k) mice. The distribution of some selected class I and II major histocompatibility complex-determined antigens was localized by immunocytochemistry with the use of anti-H-2Kk and anti-IAk monoclonal antibodies and avidin-biotin-peroxidase in unfixed, frozen lungs for light microscopy and in fixed lungs for electron microscopy. In normal control mice no class I antigens were detected in the lung either by light microscopy or by ultrastructural immunocytochemistry. After 6 to 9 days of IFN-gamma administration, class I antigens were detectable on the endothelium of major vessels and diffusely throughout the alveolar region, presumably on alveolar capillary endothelium. Class I antigens did not withstand chemical fixation, therefore, could not be localized at the ultrastructural level. In normal, control mice class II antigens were detectable on a few interstitial macrophages, on some circulating monocytes, and on elongated cells adjacent to airways and major vessels. After 6 to 9 daily injections of IFN-gamma, larger numbers of macrophages and elongated cells, believed to be dendritic cells, were present around major airways and vessels. In addition, numerous round cells stained throughout the alveolar region. By electron microscopy these round cells included intraalveolar macrophages, although not all alveolar macrophages expressed IAk, circulating monocytes in capillary lumens, and type II pneumocytes. Type I pneumocytes had no detectable IAk. Reaction product in type II cells was limited to the basolateral membranes. Airway epithelium and endothelium remained unstained. These observations indicate that in addition to monocytes/macrophages IFN-gamma induces the expression of class II antigens on type II pneumocytes.
将重组鼠γ干扰素(IFN-γ)对B10.BR(H-2k)小鼠进行6至9天的每日腹腔注射。使用抗H-2Kk和抗IAk单克隆抗体以及抗生物素蛋白-生物素-过氧化物酶,通过免疫细胞化学方法,在未固定的冰冻肺组织中进行光镜检查,以及在固定的肺组织中进行电镜检查,对一些选定的Ⅰ类和Ⅱ类主要组织相容性复合体决定的抗原分布进行定位。在正常对照小鼠中,无论是通过光镜还是超微结构免疫细胞化学,在肺中均未检测到Ⅰ类抗原。给予IFN-γ 6至9天后,在大血管内皮上可检测到Ⅰ类抗原,并且在整个肺泡区域广泛分布,推测是在肺泡毛细血管内皮上。Ⅰ类抗原不耐受化学固定,因此无法在超微结构水平上定位。在正常对照小鼠中,Ⅱ类抗原可在少数间质巨噬细胞、一些循环单核细胞以及气道和大血管附近的细长细胞上检测到。在每日注射IFN-γ 6至9天后,在主要气道和血管周围出现了大量的巨噬细胞和细长细胞,据信是树突状细胞。此外,在整个肺泡区域有大量圆形细胞被染色。通过电子显微镜观察,这些圆形细胞包括肺泡内巨噬细胞,尽管并非所有肺泡巨噬细胞都表达IAk,还有毛细血管腔内的循环单核细胞以及Ⅱ型肺细胞。Ⅰ型肺细胞未检测到IAk。Ⅱ型细胞中的反应产物仅限于基底外侧膜。气道上皮和内皮未被染色。这些观察结果表明,除单核细胞/巨噬细胞外,IFN-γ还可诱导Ⅱ型肺细胞表达Ⅱ类抗原。