首页> 美国卫生研究院文献>The Journal of Neuroscience >Developmental regulation of nicotinic ACh receptor subunit mRNAs in the rat central and peripheral nervous systems
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Developmental regulation of nicotinic ACh receptor subunit mRNAs in the rat central and peripheral nervous systems

机译:大鼠中枢神经系统和周围神经系统中烟碱型ACh受体亚基mRNA的发育调控

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摘要

In the present study we have investigated the anatomical distribution pattern of nAChR alpha 3, alpha 4, beta 2, and beta 4 subunit mRNAs during prenatal and perinatal development of the rat CNS and PNS. Three main developmental patterns have been recognized. (1) In the majority of cases studied (caudal brain, spinal cord, dorsal root ganglia, trigeminal and geniculate ganglia) all four subunit mRNAs are initially (E11–13) detected but, during subsequent prenatal development, the level of some of these subunit mRNAs (alpha 3 and beta 4 in the brain and spinal cord, alpha 4 and beta 4 in the dorsal root ganglia, alpha 4 in the visceral sensory ganglia, and alpha 3, alpha 4, and beta 4 in the somatic sensory ganglia) become undetectable. (2) In the case of the cerebral cortex a pair of subunit mRNAs (alpha 3-beta 2) is initially (E12–13) expressed followed by a repression of the alpha 3 subunit (E15) and the subsequent (E17–19) induction of the alpha 4 subunit. (3) Only some subunit mRNAs are initially (E13–15) expressed in the retina (alpha 3-alpha 4-beta 2-beta 4), parasympathetic or sympathetic motor ganglia (alpha 3-beta 2-beta 4), and vestibulo- cochlear ganglia (alpha 4-beta 2) and their level remains stable throughout prenatal and early postnatal development. Overall, in most central and peripheral structures the appearance of nAChR subunit mRNAs is precocious and temporally related to the timing of neuronal differentiation. In addition, in several structures the expression of certain subunits (alpha 3, alpha 4 or beta 4) is transient, although not beta 2. Finally, the comparison of the different regional distribution patterns suggests that a limited number of structure- specific receptor isoforms are functional during development of CNS and PNS.
机译:在本研究中,我们研究了大鼠CNS和PNS的产前和围产期发育过程中nAChR alpha 3,α4,β2和β4亚基mRNA的解剖分布模式。已经认识到三种主要的发展模式。 (1)在大多数研究的病例(尾脑,脊髓,背根神经节,三叉神经和膝状神经节)中,最初检测到所有四个亚基mRNA(E11-13),但在随后的产前发育过程中,其中一些亚基的水平亚单位mRNA(大脑和脊髓中的alpha 3和beta 4,背根神经节中的alpha 4和beta 4,内脏感觉神经节中的alpha 4,以及躯体感觉神经节中的alpha 3,alpha 4和beta 4)变得不可检测。 (2)在大脑皮层的情况下,首先表达一对亚基mRNA(alpha 3-beta 2)(E12-13),然后抑制α3亚基(E15),随后抑制(E17-19) α4亚基的诱导。 (3)最初只有一些亚基mRNA(E13-15)在视网膜(alpha 3-alpha 4-beta 2-beta 4),副交感神经或交感神经节(alpha 3-beta 2-beta 4)和前庭中表达-耳蜗神经节(α4-β2)及其水平在整个产前和产后早期均保持稳定。总体而言,在大多数中央和周边结构中,nAChR亚基mRNA的出现与神经元分化的时间有关,早熟且在时间上相关。另外,在某些结构中,某些亚基(α3,α4或β4)的表达是瞬时的,尽管不是β2。最后,不同区域分布模式的比较表明,结构特异性受体同工型的数量有限在CNS和PNS的开发过程中起作用。

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