Cunningham A C, Milne D S, Wilkes J, Dark J H, Tetley T D, Kirby J A
Department of Surgery, University of Newcastle upon Tyne, UK.
J Cell Sci. 1994 Feb;107 ( Pt 2):443-9. doi: 10.1242/jcs.107.2.443.
Highly purified populations of alveolar epithelial cells (type II pneumocytes) were isolated from human lung specimens. These cells were characterised histochemically, by demonstrating the presence of intracellular alkaline phosphatase, and morphologically, by electron microscopic demonstration of lamellar bodies and microvilli. Expression of the epithelial glycoprotein HEA-125, of MHC class I and class II (HLA-DR, -DP and -DQ) antigens and of the intercellular adhesion molecules ICAM-1, VCAM-1, LFA-3 and B7 was quantified by flow cytometry. Comparison was made between the expression of these molecules by isolated type II cells and by alveolar epithelium in normal human lung tissue after immunocytochemical staining of frozen sections of donor lung. Isolated type II pneumocytes expressed HEA-125 and class I MHC molecules and the class II MHC molecules HLA-DR and -DP; HLA-DQ was not detected. The intercellular adhesion molecule ICAM-1 was expressed constitutively at low levels but there was minimal expression of VCAM-1, LFA-3 and B7. It was not possible to differentiate type II cells from the predominant type I pneumocytes on frozen sections. Alveolar epithelium expressed HEA-125, class I MHC antigens, the class II molecules HLA-DR, and -DP and the intercellular adhesion molecule LFA-3. Expression of the adhesion molecules ICAM-1, VCAM-1 and B7 was variable. As with the isolates, HLA-DQ was not observed on alveolar epithelium. In conclusion, a reproducible method for the isolation of pure populations of human type II pneumocytes has been developed. These cells were not damaged by the isolation procedure. It is not known whether alveolar epithelium can present antigens to T lymphocytes.(ABSTRACT TRUNCATED AT 250 WORDS)
从人肺标本中分离出高度纯化的肺泡上皮细胞群体(II型肺细胞)。通过细胞内碱性磷酸酶的组织化学检测以及板层小体和微绒毛的电子显微镜观察,对这些细胞进行了组织化学和形态学特征鉴定。通过流式细胞术对上皮糖蛋白HEA - 125、MHC I类和II类(HLA - DR、- DP和 - DQ)抗原以及细胞间黏附分子ICAM - 1、VCAM - 1、LFA - 3和B7的表达进行定量。在供体肺冰冻切片免疫细胞化学染色后,比较了分离的II型细胞与正常人肺组织中肺泡上皮细胞这些分子的表达情况。分离的II型肺细胞表达HEA - 125和I类MHC分子以及II类MHC分子HLA - DR和 - DP;未检测到HLA - DQ。细胞间黏附分子ICAM - 1以低水平组成性表达,但VCAM - 1、LFA - 3和B7的表达极少。在冰冻切片上无法将II型细胞与占主导的I型肺细胞区分开来。肺泡上皮表达HEA - 125、I类MHC抗原、II类分子HLA - DR和 - DP以及细胞间黏附分子LFA - 3。黏附分子ICAM - 1、VCAM - 1和B7的表达存在差异。与分离细胞一样,肺泡上皮未观察到HLA - DQ。总之,已开发出一种可重复的方法来分离纯的人II型肺细胞群体。这些细胞未因分离过程而受损。尚不清楚肺泡上皮是否能将抗原呈递给T淋巴细胞。(摘要截短于250词)