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Kctd12和Ulk2共同作用以调节缰核中的树突形成和行为。

Kctd12 and Ulk2 partner to regulate dendritogenesis and behavior in the habenular nuclei.

作者信息

Lee Stacey, Page-McCaw Patrick, Gamse Joshua T

机构信息

Vanderbilt University, Department of Biological Sciences, Nashville, Tennessee, United States of America.

Vanderbilt University Medical Center, Department of Molecular Physiology and Biophysics, Nashville, Tennessee, United States of America.

出版信息

PLoS One. 2014 Oct 20;9(10):e110280. doi: 10.1371/journal.pone.0110280. eCollection 2014.

Abstract

The habenular nuclei of the limbic system regulate responses, such as anxiety, to aversive stimuli in the environment. The habenulae receive inputs from the telencephalon via elaborate dendrites that form in the center of the nuclei. The kinase Ulk2 positively regulates dendritogenesis on habenular neurons, and in turn is negatively regulated by the cytoplasmic protein Kctd12. Given that the habenulae are a nexus in the aversive response circuit, we suspected that incomplete habenular dendritogenesis would have profound implications for behavior. We find that Ulk2, which interacts with Kctd12 proteins via a small proline-serine rich domain, promotes branching and elaboration of dendrites. Loss of Kctd12 results in increased branching/elaboration and decreased anxiety. We conclude that fine-tuning of habenular dendritogenesis during development is essential for appropriate behavioral responses to negative stimuli.

摘要

边缘系统的缰核调节对环境中厌恶刺激的反应,如焦虑。缰核通过在核中心形成的精细树突从端脑接收输入。激酶Ulk2正向调节缰核神经元的树突生成,而细胞质蛋白Kctd12则对其进行负向调节。鉴于缰核是厌恶反应回路中的一个枢纽,我们怀疑缰核树突生成不完全会对行为产生深远影响。我们发现,Ulk2通过一个富含脯氨酸 - 丝氨酸的小结构域与Kctd12蛋白相互作用,促进树突的分支和细化。Kctd12的缺失导致分支/细化增加和焦虑减少。我们得出结论,发育过程中缰核树突生成的微调对于对负面刺激做出适当的行为反应至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08da/4203773/85f8e855fbb3/pone.0110280.g001.jpg

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