[AQP1过表达对小鼠雪旺细胞形态和水转运的影响]。

中华整形外科杂志 Pub Date : 2016-01-01
Jie Zhang, Honghua Yang, Li Peng, Hua Jiang
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引用次数: 0

摘要

目的:通过研究AQP1基因表达与雪旺细胞肿胀的关系,探讨AQP1基因在损伤后面神经水肿中的作用。方法:采用免疫荧光染色法检测小鼠面神经组织雪旺细胞AQP1的表达。采用慢病毒转导转基因方案特异性上调雪旺细胞AQP1的表达。通过相差显微镜观察lentii - aqp1和CTRL(空载体)转导的细胞每隔24 h进行基因过表达,共6天。从给药当天到第6天,每天测量CTRL和lentii - aqp1处理细胞的细胞体积。结果:雪旺细胞原代培养维持了高水平的AQP1水通道,是研究AQP1在面神经中的作用的理想细胞模型。与CTRL慢病毒相比,lentii -AQP1感染雪旺细胞后AQP1 mRNA和蛋白的表达显著升高(P < 0.05)。lentii - aqp1在培养的雪旺细胞中引起细胞肿胀,通过细胞体积测定证实(P < 0.01)。结论:AQP1是培养雪旺细胞快速水转运的重要因子。它在面神经水肿中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effects of AQP1 overexpression on morphology and water transport in mouse Schwann cells].

Objective: To determine the effect of AQP1 gene on facial nerve edema following injury through investigation of the relationship between the expression of AQP1 gene and Schwann cells swelling.

Methods: The AQP1 expression in Schwann cells of mouse facial nerve tissues was detected by immunofluorescent staining. The transgenic protocol by lentivirus transduction was used to specifically upregulate AQP1 expression in Schwann cells. Lenti-AQP1 and CTRL (empty vector) transduced cells were observed during gene overexpression every 24 h for 6 days by using phase contrast microscopy. Cell volume of CTRL and Lenti-AQP1 treated cells was measured daily from the day of treatment, through day 6.

Results: Schwann cell primary cultures maintained a high level of AQP1 water channels, representing an ideal cell model to study the role of AQP1 in the facial nerve. The expression of AQP1 mRNA and protein in Schwann cells infected with the Lenti-AQP1 was increased significantly compared with CTRL lentivirus (P < 0.05). Lenti-AQP1 caused cell swelling in cultured Schwann cells, as validated by cell volume determinations (P < 0.01).

Conclusions: AQP1 is an important factor responsible for the fast water transport of cultured Schwann cells. It plays an important role in facial nerve edema.

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