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大鼠神经垂体中的BC1 RNA与加压素mRNA:脱水和再水化过程中的轴突分隔及差异调节

BC1 RNA and vasopressin mRNA in rat neurohypophysis: axonal compartmentalization and differential regulation during dehydration and rehydration.

作者信息

Trembleau A, Melia K R, Bloom F E

机构信息

Scripps Research Institute, Department of Neuropharmacology, La Jolla, CA 92037, USA.

出版信息

Eur J Neurosci. 1995 Nov 1;7(11):2249-60. doi: 10.1111/j.1460-9568.1995.tb00646.x.

Abstract

Brain cytoplasmic 1 (BC1) RNA is a small non-translated RNA polymerase III transcript. Because this RNA can be detected in the rat posterior pituitary with 35S in situ hybridization autoradiography, it has been hypothesized that this RNA might be transported in the axons of hypothalamo-neurohypophyseal neurons. In the present study, we aimed to determine the cellular localization of BC1 more precisely by using non-radioactive in situ hybridization of BC1 RNA at both the light and electron microscopic levels. Our studies revealed that BC1 RNA was indeed located intra-axonally. Furthermore, BC1 RNA was abundant within a subset of axonal swellings and/or terminals, and was also found in discrete cytoplasmic domains of undilated axonal segments. Using a semiquantitative in situ hybridization approach, we have measured and compared the changes in BC1 RNA and arginine vasopressin (AVP) mRNA during dehydration (chronic salt-loading) and rehydration. Chronic salt-loading significantly increased both BC1 RNA and AVP mRNA. The increase in BC1 RNA labelling (2.5-fold), however, was modest and somewhat less enduring than the increase in AVP mRNA labelling (13-fold). Upon rehydration, both the BC1 and vasopressin transcripts in the posterior pituitary rapidly returned to control values. In conclusion, like vasopressin mRNA, BC1 RNA is transported in axons of the hypothalamo-neurohypophyseal system where it aggregates in a subset of axonal swellings, and its axonal transport is similarly regulated. Therefore, we propose that BC1 RNA might be involved in the axonal targeting, docking and/or transport of AVP or other axonal mRNAs.

摘要

脑细胞质1(BC1)RNA是一种小的非翻译RNA聚合酶III转录本。由于这种RNA可以通过35S原位杂交放射自显影在大鼠垂体后叶中检测到,因此有人推测这种RNA可能在下丘脑 - 神经垂体神经元的轴突中运输。在本研究中,我们旨在通过在光学和电子显微镜水平上使用BC1 RNA的非放射性原位杂交来更精确地确定BC1的细胞定位。我们的研究表明,BC1 RNA确实位于轴突内。此外,BC1 RNA在轴突肿胀和/或终末的一个子集中丰富,并且也存在于未扩张轴突段的离散细胞质区域中。使用半定量原位杂交方法,我们测量并比较了脱水(慢性盐负荷)和补液过程中BC1 RNA和精氨酸加压素(AVP)mRNA的变化。慢性盐负荷显著增加了BC1 RNA和AVP mRNA。然而,BC1 RNA标记的增加(2.5倍)是适度的,并且比AVP mRNA标记的增加(13倍)持续时间稍短。补液后,垂体后叶中的BC1和加压素转录本迅速恢复到对照值。总之,与加压素mRNA一样,BC1 RNA在下丘脑 - 神经垂体系统的轴突中运输,在那里它聚集在轴突肿胀的一个子集中,并且其轴突运输受到类似的调节。因此,我们提出BC1 RNA可能参与AVP或其他轴突mRNA的轴突靶向、对接和/或运输。

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