Maronde E, Schomerus C, Stehle J H, Korf H W
Anatomisches Institut II, Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt/Main, Germany.
Biol Cell. 1997 Nov;89(8):505-11. doi: 10.1016/s0248-4900(98)80006-3.
Phosphorylation of the transcription factor CREB appears as an important step in the signal transduction cascade that activates melatonin biosynthesis in the mammalian pineal organ. We have studied the mechanisms causing CREB phosphorylation by immunocytochemical and immunochemical demonstration of phosphorylated CREB (pCREB) in isolated, immunocytochemically identified rat pinealocytes kept in vitro and in the rat pineal organ in situ. Norepinephrine (NE), the most potent stimulator of the melatonin biosynthesis was shown to induce pCREB immunoreaction (i.r.) in the vast majority of pinealocytes in a time- and dose-dependent manner. This response was elicited by stimulation of beta-adrenergic receptors resulting in an increase in the intracellular cAMP concentration. Activation of alpha 1-adrenergic receptors that causes a rise in intracellular calcium via stimulation of intracellular stores and subsequent increase in calcium influx did not evoke pCREB ir on its own and did not potentiate the beta-adrenergic response. VIP and PACAP that activate the melatonin biosynthesis to a lesser extent than NE induced pCREB ir in only 50-60% of the pinealocytes. Immunoblotting showed that a protein of 43 kDa corresponding to CREB accounts for the pCREB ir and confirmed that VIP and PACAP are less effective in inducing CREB phosphorylation than NE. The amount of total (phosphorylated and unphosphorylated) CREB was not changed upon stimulation of the cells with NE, VIP or PACAP. In an attempt to identify the protein kinase catalyzing CREB phosphorylation in rat pinealocytes, the cAMP-dependent protein kinases (cAK) present in the rat pineal were identified with the use of antibodies recognizing different catalytic and regulatory subunits. Application of cAK agonists and antagonists showed that the cAK type II is responsible for CREB phosphorylation. Correlations between the melatonin concentration in the medium and the CREB phosphorylation in pinealocytes revealed a tight connection between these two parameters. Phosphorylation of CREB appears important for the stimulation of melatonin biosynthesis also under natural conditions because our investigations of whole pineal organs taken from rats during different time points of the 24 h light-dark cycle revealed a strong induction of pCREB ir in the first part of the night.
转录因子CREB的磷酸化似乎是激活哺乳动物松果体中褪黑素生物合成的信号转导级联反应中的一个重要步骤。我们通过免疫细胞化学和免疫化学方法,对体外培养的、经免疫细胞化学鉴定的大鼠松果体细胞以及原位大鼠松果体器官中磷酸化CREB(pCREB)进行了研究,以探讨导致CREB磷酸化的机制。去甲肾上腺素(NE)是褪黑素生物合成最有效的刺激物,已证明它能以时间和剂量依赖的方式在绝大多数松果体细胞中诱导pCREB免疫反应(i.r.)。这种反应是由β-肾上腺素能受体的刺激引起的,导致细胞内cAMP浓度升高。通过刺激细胞内储存库并随后增加钙内流从而使细胞内钙升高的α1-肾上腺素能受体的激活,本身并不会引起pCREB免疫反应,也不会增强β-肾上腺素能反应。血管活性肠肽(VIP)和垂体腺苷酸环化酶激活肽(PACAP)对褪黑素生物合成的激活程度低于NE,它们仅在50%-60%的松果体细胞中诱导pCREB免疫反应。免疫印迹显示,与CREB相对应的43 kDa蛋白是pCREB免疫反应的原因,并证实VIP和PACAP在诱导CREB磷酸化方面比NE的效果差。用NE、VIP或PACAP刺激细胞后,总(磷酸化和未磷酸化)CREB的量没有变化。为了确定催化大鼠松果体细胞中CREB磷酸化的蛋白激酶,我们使用识别不同催化亚基和调节亚基的抗体,鉴定了大鼠松果体中存在的cAMP依赖性蛋白激酶(cAK)。应用cAK激动剂和拮抗剂表明,II型cAK负责CREB的磷酸化。培养基中褪黑素浓度与松果体细胞中CREB磷酸化之间的相关性揭示了这两个参数之间的紧密联系。在自然条件下,CREB的磷酸化对于刺激褪黑素生物合成似乎也很重要,因为我们对取自24小时明暗周期不同时间点的大鼠整个松果体器官的研究表明,在夜间的第一部分,pCREB免疫反应有强烈的诱导。