Bering Tenna, Hertz Henrik, Rath Martin Fredensborg
Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Front Physiol. 2021 Oct 27;12:706433. doi: 10.3389/fphys.2021.706433. eCollection 2021.
The central circadian clock resides in the suprachiasmatic nucleus (SCN) of the hypothalamus, but an SCN-dependent molecular circadian oscillator is present in the cerebellar cortex. Recent findings suggest that circadian release of corticosterone is capable of driving the circadian oscillator of the rat cerebellum. To determine if additional neuroendocrine signals act to shape cerebellar clock gene expression, we here tested the role of the thyroid hormone triiodothyronine (T3) in regulation of the cerebellar circadian oscillator. In cultured cerebellar granule cells from mixed-gender neonatal rats, T3 treatment affected transcript levels of the clock genes , , , and , suggesting that T3 acts directly on granule cells to control the circadian oscillator. We then used two different protocols to test the role of T3 in adult female rats: Firstly, a single injection of T3 did not influence clock gene expression in the cerebellum. Secondly, we established a surgical rat model combining SCN lesion with a programmable micropump infusing circadian physiological levels of T3; however, rhythmic infusion of T3 did not reestablish differential clock gene expression between day and night in SCN lesioned rats. To test if the effects of T3 observed were related to the developmental stage, acute injections of T3 were performed in mixed-gender neonatal rats ; this procedure significantly affected cerebellar expression of the clock genes , , , and . Developmental comparisons showed rhythmic expression of all clock genes analyzed in the cerebellum of adult rats only, whereas T3 responsiveness was limited to neonatal animals. Thus, T3 shapes cerebellar clock gene profiles in early postnatal stages, but it does not represent a systemic circadian regulatory mechanism linking the SCN to the cerebellum throughout life.
中枢生物钟位于下丘脑的视交叉上核(SCN),但在小脑皮质中也存在依赖于SCN的分子昼夜节律振荡器。最近的研究结果表明,皮质酮的昼夜释放能够驱动大鼠小脑的昼夜节律振荡器。为了确定是否有其他神经内分泌信号参与塑造小脑生物钟基因的表达,我们在此测试了甲状腺激素三碘甲状腺原氨酸(T3)在调节小脑昼夜节律振荡器中的作用。在来自新生雌雄混合大鼠的培养小脑颗粒细胞中,T3处理影响了生物钟基因、、、和的转录水平,这表明T3直接作用于颗粒细胞以控制昼夜节律振荡器。然后,我们使用两种不同的方案来测试T3在成年雌性大鼠中的作用:首先,单次注射T3不影响小脑中生物钟基因的表达。其次,我们建立了一种手术大鼠模型,将SCN损伤与可编程微型泵相结合,以注入昼夜生理水平的T3;然而,有节律地注入T3并没有在SCN损伤的大鼠中重新建立昼夜之间不同的生物钟基因表达。为了测试观察到的T3的作用是否与发育阶段有关,我们对新生雌雄混合大鼠进行了急性T3注射;这一过程显著影响了生物钟基因、、、和在小脑中的表达。发育比较表明,仅在成年大鼠的小脑中分析的所有生物钟基因都有节律性表达,而T3反应性仅限于新生动物。因此,T3在出生后早期塑造了小脑生物钟基因谱,但它并不代表一种在整个生命过程中将SCN与小脑联系起来的系统性昼夜调节机制。