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甲状腺激素在视网膜发育、存活及疾病中的信号传导

Thyroid Hormone Signaling in Retinal Development, Survival, and Disease.

作者信息

Yang Fan, Ma Hongwei, Ding Xi-Qin

机构信息

University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.

University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.

出版信息

Vitam Horm. 2018;106:333-349. doi: 10.1016/bs.vh.2017.05.001. Epub 2017 Jun 19.

Abstract

Thyroid hormone (TH) is essential in numerous physiological functions and developmental processes. It acts through TH receptors (TRs) to regulate gene expression. The retina is the light-sensitive tissue lining the back of the eye and functions as the first step of the visual process. Rod and cone photoreceptors are specialized sensory neurons in the retina that initiate phototransduction. Rods are responsible for dim light vision, whereas cones are responsible for daytime vision, color vision, and visual acuity. TH signaling regulates retinal development and maintenance. The requirement of TH signaling is typically manifested as its regulation in the cone maturation and expression of the light-sensing pigment protein (cone opsin). There are two components of this regulation. First, TRβ2, a TH-activated transcription factor, is expressed in immature cones and regulates cone differentiation and cone opsin expression; activation of TRβ2 suppresses the expression of short-wave-sensitive opsin 1, induces the expression of medium-wave-sensitive opsin 1, and promotes dorsal-ventral opsin patterning. Second, hypothyroid mouse models display abnormalities in cone opsin expression, supporting the necessity of TH itself in retinal development. TH has been linked to photoreceptor survival. Excessive TH signaling leads to death of developing photoreceptors in healthy and diseased retina, whereas suppressing TH signaling preserves cones in mouse models of retinal degeneration. Some eye diseases, including age-related macular degeneration, have been associated with elevated circulation TH levels. Future work should aim to better understand how TH regulates retinal development, functionality, and survival, to examine the role of TH signaling in the pathogenesis of retinal degeneration, and to explore the potential of TH signaling manipulation for photoreceptor protection. Hopefully, these knowledge bases will lead to the identification of novel strategies for retinal disease prevention and management.

摘要

甲状腺激素(TH)在众多生理功能和发育过程中至关重要。它通过甲状腺激素受体(TRs)发挥作用来调节基因表达。视网膜是衬于眼球后部的光敏感组织,是视觉过程的第一步。视杆和视锥光感受器是视网膜中的特殊感觉神经元,可启动光转导。视杆负责暗光视觉,而视锥负责白昼视觉、色觉和视敏度。TH信号通路调节视网膜的发育和维持。TH信号通路的需求通常表现为其对视锥成熟和光感受色素蛋白(视锥视蛋白)表达的调节。这种调节有两个方面。首先,TRβ2是一种TH激活的转录因子,在未成熟视锥中表达,调节视锥分化和视锥视蛋白表达;TRβ2的激活抑制短波敏感视蛋白1的表达,诱导中波敏感视蛋白1的表达,并促进背腹视蛋白模式形成。其次,甲状腺功能减退小鼠模型在视锥视蛋白表达上表现出异常,支持了TH本身在视网膜发育中的必要性。TH与光感受器存活有关。TH信号通路过度会导致健康和患病视网膜中发育中的光感受器死亡,而抑制TH信号通路则可在视网膜变性小鼠模型中保护视锥。一些眼部疾病,包括年龄相关性黄斑变性,与循环中TH水平升高有关。未来的工作应旨在更好地理解TH如何调节视网膜发育、功能和存活,研究TH信号通路在视网膜变性发病机制中的作用,并探索操纵TH信号通路以保护光感受器的潜力。希望这些知识库能促成视网膜疾病预防和管理新策略的发现。

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