Castell Xavier, Cheviron Nathalie, Barnier Jean-Vianney, Diebler Marie-Françoise
Laboratoire de Neurobiologie Cellulaire et Moléculaire, CNRS, 91198 Gif-sur-Yvette, Cedex, France.
Neurochem Res. 2003 Apr;28(3-4):557-64. doi: 10.1023/a:1022829608540.
Involvement of different protein kinases regulated by cAMP and implication of muscarinic receptors in the regulation of choline acetyltransferase (ChAT) and vesicular acetylcholine transporter (VAChT) mRNA levels and ChAT activity has been studied in NG108-15 cells. Dibutyryl cAMP enhanced both ChAT and VAChT mRNA levels and stimulated ChAT activity. Muscarinic stimulation or inhibition did not change ChAT activity or the receptor subtype mRNA pattern. MEK1/2 did not affect the regulation of ChAT and VAChT mRNA levels. However, PKA plays a major role in regulating ChAT and VAChT mRNA levels, because H89 decreased both. Strikingly, inhibition of PI3K by LY294002 had two opposite effects: ChAT mRNA level was decreased and VAChT mRNA level was increased. Such a result consolidates the observation that ChAT and VAChT genes, despite their unusual organization in a single "cholinergic locus," can be differentially or synergistically regulated, depending on the activated signaling pathways.
在NG108 - 15细胞中,研究了由环磷酸腺苷(cAMP)调节的不同蛋白激酶的参与情况,以及毒蕈碱受体在调节胆碱乙酰转移酶(ChAT)和囊泡乙酰胆碱转运体(VAChT)mRNA水平及ChAT活性中的作用。二丁酰环磷酸腺苷增强了ChAT和VAChT的mRNA水平,并刺激了ChAT活性。毒蕈碱刺激或抑制并未改变ChAT活性或受体亚型mRNA模式。丝裂原活化蛋白激酶激酶1/2(MEK1/2)不影响ChAT和VAChT mRNA水平的调节。然而,蛋白激酶A(PKA)在调节ChAT和VAChT mRNA水平中起主要作用,因为H89降低了两者的水平。令人惊讶的是,LY294002对磷脂酰肌醇-3激酶(PI3K)的抑制产生了两种相反的作用:ChAT mRNA水平降低,而VAChT mRNA水平升高。这一结果证实了以下观察结果:尽管ChAT和VAChT基因在单一“胆碱能位点”中具有不同寻常的组织方式,但它们可根据激活的信号通路进行差异或协同调节。