Yueduan Wei, Jinhua Zuo, Changling Ding, Yuhong Zhu, Lifang Wang, Bing Song, Jing Wang
Dept. of Oral and Maxillofacial Surgery, The Affiliated Hospital of Binzhou Medical College, Binzhou 256600, China.
Dept. of Pharmacy, The Affiliated Hospital of Binzhou Medical College, Binzhou 256600, China.
Hua Xi Kou Qiang Yi Xue Za Zhi. 2017 Dec 1;35(6):583-587. doi: 10.7518/hxkq.2017.06.004.
This research aims to further explore the expression and significance of proliferating cell nuclear antigen (PCNA) and P53 in regenerating rat atrophy parotid gland from the gene and protein levels.
One hundred and two Wistar rats were randomly divided into experimental and control groups; the former group's duct was ligated and then released respectively in 7 (Group A) and 14 days (Group B). Fresh parotid specimens were obtained at 0, 3, 5, 7, 10, 14, 21, and 28 days after being released. Hematoxylin-eosin staining method was used to observe the morphological changes of the parotid gland. The significance of P53 and PCNA in two groups was resolved by real-time fluorescence quantitative polymerase china reaction and Western blot.
Acinar cells aoptosis and duct cells proliferation occurred when the occlusion of the parotid duct was reversed on days 7 and 14. The expression of P53 was higher than that of PCNA, and they reached the peak at the third and fifth days after groups A and B regenerated, respectively. This finding was significantly different compared with the control (P<0.01). P53 and PCNA contents decreased gradually; acinar and duct gradually returned to normal morphology; PCNA and P53 contents gradually close to the normal control group.
After ligating the parotid duct, P53 was highly expressed, and induced parotid gland atrophy. Mean-while, PCNA was highly expressed, which then decreased inducing gland recovery.
本研究旨在从基因和蛋白水平进一步探讨增殖细胞核抗原(PCNA)和P53在大鼠腮腺萎缩再生过程中的表达及意义。
将102只Wistar大鼠随机分为实验组和对照组;实验组分别于结扎腮腺导管7天(A组)和14天(B组)后再通。于再通后0、3、5、7、10、14、21和28天获取新鲜腮腺标本。采用苏木精-伊红染色法观察腮腺形态学变化。通过实时荧光定量聚合酶链反应和蛋白质印迹法分析两组中P53和PCNA的意义。
在第7天和第14天腮腺导管再通时,腺泡细胞发生凋亡,导管细胞增殖。P53的表达高于PCNA,且分别在A组和B组再生后的第3天和第5天达到峰值。与对照组相比,这一结果有显著差异(P<0.01)。P53和PCNA含量逐渐降低;腺泡和导管逐渐恢复正常形态;PCNA和P53含量逐渐接近正常对照组。
结扎腮腺导管后,P53高表达,诱导腮腺萎缩。同时,PCNA高表达,随后降低,诱导腺体恢复。