Baker Olga J, Camden Jean M, Ratchford Ann M, Seye Cheikh I, Erb Laurie, Weisman Gary A
Department of Biochemistry, University of Missouri-Columbia, 540E Life Sciences Center, 1201 Rollins Road, Columbia, MO 65211-7310, USA.
Arch Oral Biol. 2006 May;51(5):359-70. doi: 10.1016/j.archoralbio.2005.10.004. Epub 2005 Dec 5.
In rat submandibular gland (SMG), the P2Y1 receptor (P2Y1R) mediates increases in the intracellular calcium concentration, [Ca2+]i that diminish as the animal ages from 1 to 4-6 weeks. However, P2Y1R mRNA levels do not change with age, suggesting that the age-dependent decrease in the [Ca2+]i response to P2Y1R agonists may be due to alterations in the activity of a component of the P2Y1R signalling pathway.
To assess whether the decrease in P2Y1R-mediated intracellular calcium signalling in SMG cells as rats age is due to a decrease in P2Y1R coupling to G proteins or to a decrease in the expression of a cognate G protein.
SMG cells were isolated from Sprague-Dawley rats. P2Y1R function was assessed by measuring 2-MeSADP-induced increases in [Ca2+]i and ERK1/2 activation. P2Y(1)R-mediated activation of G proteins was determined by the [35S]GTPgammaS binding assay. Gq protein expression was determined by RT-PCR, Northern, and Western analysis.
In SMG cells from 1-week-old rats, two bands (52 and 42kDa) were detected using anti-Galpha14 antibody, whereas in SMG cells from 4- to 6-week-old rats only the 42 kDa band was detected. Furthermore, 2-MeSADP-induced GTPgamma35S binding to Galpha14 and Galphaq/11 decreases in SMG cells from 4- to 6-week-old rats as compared to 1-week-old rats.
These findings suggest that the age-dependent decrease in P2Y1R-mediated intracellular calcium signalling in rat SMG cells is due to a loss of 52 kDa Galpha14 and indicate the differential coupling of the P2Y1R to Galpha14 and Galphaq/11 as the gland develops.
在大鼠颌下腺(SMG)中,P2Y1受体(P2Y1R)介导细胞内钙浓度[Ca2+]i升高,随着动物从1周龄长到4 - 6周龄,该升高幅度逐渐减小。然而,P2Y1R mRNA水平并不随年龄变化,这表明P2Y1R激动剂引起的[Ca2+]i反应随年龄下降可能是由于P2Y1R信号通路某一成分活性改变所致。
评估大鼠随着年龄增长,SMG细胞中P2Y1R介导的细胞内钙信号传导减少是由于P2Y1R与G蛋白偶联减少还是同源G蛋白表达减少。
从Sprague-Dawley大鼠分离出SMG细胞。通过测量2-甲基硫代二磷酸腺苷(2-MeSADP)诱导的[Ca2+]i升高和细胞外调节蛋白激酶1/2(ERK1/2)激活来评估P2Y1R功能。通过[35S]GTPγS结合试验确定P2Y(1)R介导的G蛋白激活。通过逆转录聚合酶链反应(RT-PCR)、Northern印迹和Western印迹分析确定Gq蛋白表达。
在1周龄大鼠的SMG细胞中,使用抗Gα14抗体检测到两条带(52 kDa和42 kDa),而在4 - 6周龄大鼠的SMG细胞中仅检测到42 kDa的带。此外,与1周龄大鼠相比,4 - 6周龄大鼠的SMG细胞中,2-MeSADP诱导的GTPγ35S与Gα14和Gαq/11的结合减少。
这些发现表明,大鼠SMG细胞中P2Y1R介导的细胞内钙信号传导随年龄下降是由于52 kDa Gα14缺失,并表明随着腺体发育,P2Y1R与Gα14和Gαq/11的偶联存在差异。