Shariatmadari Ramin, Sipilä Petra, Vierula Matti, Törnquist Kid, Huhtaniemi Ilpo, Poutanen Matti
Departments of Physiology, Institute of Biomedicine, University of Turku, Turku, Finland.
Biol Reprod. 2003 Apr;68(4):1185-92. doi: 10.1095/biolreprod.102.007419. Epub 2002 Oct 30.
In the present study, we developed a novel method to analyze the calcium (Ca2+) signal in living slices of mouse caput epididymides by applying calcium imaging on Fura-2-loaded vibratome slices. The data revealed that in epithelial cells of mouse caput epididymides, ATP induces a rapid Ca2+ signal that is sustained after 60 sec. Preincubating the sections in Ca2+-free medium in the presence of EGTA did not affect the amplitude of the ATP-induced Ca2+ signal, indicating the presence of P2Y type purinergic receptors and phospholipase C activity. Furthermore, ATP induced a similar Ca2+ signal in the different subregions of caput epididymides. The P2X type ion-gated purinergic receptors could also be responsible for the ATP-induced Ca2+ signal because immunohistochemical and reverse transcriptase-polymerase chain reaction analyses showed that P2X1, P2X2, P2X4, P2X7, P2Y1, and P2Y2 receptors were expressed in the epididymis. We propose that P2X and P2Y receptor expression is vital for the normal function of epididymal epithelium and sperm maturation. Furthermore, the method we developed allows us to analyze the activity of various G protein-coupled receptors in intact epithelial cells of mouse epididymides, and other reproductive tissues as well.
在本研究中,我们开发了一种新方法,通过对装载Fura-2的振动切片机切片进行钙成像,来分析小鼠附睾头活体切片中的钙(Ca2+)信号。数据显示,在小鼠附睾头的上皮细胞中,ATP诱导出一种快速的Ca2+信号,该信号在60秒后持续存在。在EGTA存在的情况下,将切片在无Ca2+培养基中预孵育并不影响ATP诱导的Ca2+信号的幅度,这表明存在P2Y型嘌呤能受体和磷脂酶C活性。此外,ATP在附睾头的不同亚区域诱导出类似的Ca2+信号。P2X型离子门控嘌呤能受体也可能是ATP诱导的Ca2+信号的原因,因为免疫组织化学和逆转录聚合酶链反应分析表明,P2X1、P2X2、P2X4、P2X7、P2Y1和P2Y2受体在附睾中表达。我们认为,P2X和P2Y受体的表达对于附睾上皮的正常功能和精子成熟至关重要。此外,我们开发的方法使我们能够分析小鼠附睾以及其他生殖组织完整上皮细胞中各种G蛋白偶联受体的活性。