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钙黏蛋白-16通过内分泌信号调节斑马鱼的听觉感觉门控。

Cadherin-16 regulates acoustic sensory gating in zebrafish through endocrine signaling.

作者信息

Schloss Susannah S, Marshall Zackary Q, Santistevan Nicholas J, Gjorcheska Stefani, Stenzel Amanda, Barske Lindsey, Nelson Jessica C

机构信息

Department of Cell and Developmental Biology; University of Colorado Anschutz Medical Campus School of Medicine, Aurora, Colorado, United States of America.

Division of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio, United States of America.

出版信息

PLoS Biol. 2025 May 2;23(5):e3003164. doi: 10.1371/journal.pbio.3003164. eCollection 2025 May.

Abstract

Sensory thresholds enable animals to regulate their behavioral responses to environmental threats. Despite the importance of sensory thresholds for animal behavior and human health, we do not yet have a full appreciation of the underlying molecular-genetic and circuit mechanisms. The larval zebrafish acoustic startle response provides a powerful system to identify molecular mechanisms underlying establishment of sensory thresholds and plasticity of thresholds through mechanisms like habituation. Using this system, we identify Cadherin-16 as a previously undescribed regulator of sensory gating. We demonstrate that Cadherin-16 regulates sensory thresholds via an endocrine organ, the corpuscle of Stannius (CS), which is essential in zebrafish for regulating Ca2+ homeostasis. We further show that Cadherin-16 regulates whole-body calcium and ultimately behavior through the hormone Stanniocalcin 1l (Stc1l), and the IGF-regulatory metalloprotease, Papp-aa. Finally, we demonstrate the importance of the CS through ablation experiments that reveal its role in promoting normal acoustic sensory gating. Together, our results uncover a previously undescribed brain non-autonomous pathway for the regulation of behavior and underscore Ca2+ homeostasis as a critical process underlying sensory gating in vivo.

摘要

感觉阈值使动物能够调节其对环境威胁的行为反应。尽管感觉阈值对动物行为和人类健康很重要,但我们尚未完全了解其潜在的分子遗传和神经回路机制。斑马鱼幼体的听觉惊吓反应提供了一个强大的系统,可用于识别感觉阈值建立和通过习惯化等机制实现阈值可塑性的潜在分子机制。利用这个系统,我们确定钙黏蛋白-16是一种先前未被描述的感觉门控调节因子。我们证明,钙黏蛋白-16通过一个内分泌器官——斯坦尼小体(CS)来调节感觉阈值,CS对斑马鱼调节钙稳态至关重要。我们进一步表明,钙黏蛋白-16通过激素斯坦尼钙素1l(Stc1l)和胰岛素样生长因子调节金属蛋白酶Papp-aa来调节全身钙水平并最终影响行为。最后,我们通过消融实验证明了CS的重要性,该实验揭示了其在促进正常听觉感觉门控中的作用。总之,我们的研究结果揭示了一条先前未被描述的调节行为的脑非自主通路,并强调钙稳态是体内感觉门控的关键过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/289d/12077787/825e6ee4e44d/pbio.3003164.g001.jpg

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