Wang Yan-rui, Ma Xi-tao, Wang Si-qin, Kong Ling-fei, Yang Zhi-gang
Respiratory Department of Henan Provincial People's Hospital, Zhengzhou 450003, China.
Zhonghua Jie He He Hu Xi Za Zhi. 2007 Oct;30(10):767-70.
To investigate the changes and significance of cell apoptosis, Fas/FasL and P53 protein in epithelial cells from patients with idiopathic pulmonary fibrosis (IPF).
Cell apoptosis and the expressions of Fas/FasL and P53 protein in lung tissues from 12 patients with IPF (IPF group) and 10 normal controls (control group) were detected by terminal deoxynucleotide transferase-mediated deoxyuridine triphosphate-biotin nick end-labeling (TUNEL) and immunohistochemistry.
Compared with the control group (0/10), the percentage of apoptosis in alveolar epithelial cells and bronchial cells of the IPF group (12/12) was higher. The percentage of Fas, FasL and P53 protein expressions (12/12, 12/12, 11/12) in alveolar epithelial cells of the IPF group were higher than those of the control group (5/10, 2/10, 0/10); and the percentage of Fas, FasL and P53 protein expressions (12/12, 12/12, 11/12) in bronchial cells of the IPF group were also higher than those of the control group (6/10, 3/10, 0/10). There was a significant correlation between the percentage of apoptosis and Fas/FasL and P53 protein expression (r=0.625-0.839, all P<0.01). The correlation of the Fas/FasL and P53 protein expression was also significant (r=0.571-0.760, all P<0.01).
The apoptosis percentage of epithelial cells and the expression of Fas/FasL and P53 protein are up-regulated in lung tissues of IPF, which may play an important role in the development of the disease.
探讨特发性肺纤维化(IPF)患者上皮细胞中细胞凋亡、Fas/FasL和P53蛋白的变化及意义。
采用末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸生物素缺口末端标记法(TUNEL)和免疫组织化学法检测12例IPF患者(IPF组)和10例正常对照者(对照组)肺组织中的细胞凋亡情况以及Fas/FasL和P53蛋白的表达。
与对照组(0/10)相比,IPF组(12/12)肺泡上皮细胞和支气管细胞的凋亡率更高。IPF组肺泡上皮细胞中Fas、FasL和P53蛋白表达阳性率(12/12、12/12、11/12)高于对照组(5/10、2/10、0/10);IPF组支气管细胞中Fas、FasL和P53蛋白表达阳性率(12/12、12/12、11/12)也高于对照组(6/10、3/10、0/10)。细胞凋亡率与Fas/FasL和P53蛋白表达之间存在显著相关性(r=0.625 - 0.839,均P<0.01)。Fas/FasL与P53蛋白表达之间的相关性也很显著(r=0.571 - 0.760,均P<0.01)。
IPF肺组织中上皮细胞凋亡率及Fas/FasL和P53蛋白表达上调,这可能在疾病发展中起重要作用。