Trindade Marlene, Silva Nádia, Rodrigues Joana, Kawakami Koichi, Campinho Marco A
Algarve Biomedical Center-Research Institute, Universidade do Algarve, Faro, Portugal.
Center for Marine Sciences of the University of the Algarve, Faro, Portugal.
Commun Biol. 2025 Jul 1;8(1):960. doi: 10.1038/s42003-025-08404-1.
Thyroid hormone (TH) signaling is important and necessary for proper neurodevelopment. Inadequate levels of maternally derived THs (MTH) supply affect target gene expression profiles, which are fundamental for the brain's normal growth, maturation, and function. The monocarboxylate transporter 8 (SLC16A2, MCT8) is the main TH transporter present in the brain during embryonic development, and mutations in this transporter lead to a rare and debilitating human condition known as the Allan-Herndon-Dudley Syndrome (AHDS). This mutation affects the capacity for intracellular transport of the hormone, leading to impaired brain development that constitutes the main pathophysiological basis of AHDS. Like humans, zebrafish embryos express slc16a2 that transports exclusively T3 at zebrafish physiological temperature. Studies in zebrafish Mct8 knockdown (KD) models found impaired hindbrain vasculature development. Here, using zebrafish Mct8 KD and knockout (KO) models, we shed light on the maternal T3 (MT3)-dependent developmental mechanism behind hindbrain vasculature development. We first demonstrate that MT3-regulates hindbrain vegfaa expression. We provide evidence that hindbrain neurons are not the source of vegfaa, instead, restricted pax6a+ neuroprogenitor cells (NPCs) instruct central arteries (CtAs) ingression into the hindbrain. Therefore, MT3 acts as an integrator, providing the regulatory cues necessary for the timely ingression of the CtAs into the hindbrain.
甲状腺激素(TH)信号传导对于正常的神经发育至关重要且必不可少。母源性甲状腺激素(MTH)供应不足会影响靶基因表达谱,而这是大脑正常生长、成熟和功能的基础。单羧酸转运蛋白8(SLC16A2,MCT8)是胚胎发育期间大脑中主要的甲状腺激素转运蛋白,该转运蛋白的突变会导致一种罕见且使人衰弱的人类疾病,即艾伦 - 赫恩登 - 达德利综合征(AHDS)。这种突变会影响激素的细胞内运输能力,导致大脑发育受损,这构成了AHDS的主要病理生理基础。与人类一样,斑马鱼胚胎表达slc16a2,在斑马鱼生理温度下,该蛋白仅转运T3。对斑马鱼Mct8基因敲低(KD)模型的研究发现后脑血管发育受损。在此,我们使用斑马鱼Mct8 KD和基因敲除(KO)模型,揭示了后脑血管发育背后依赖母源性T3(MT3)的发育机制。我们首先证明MT3调节后脑vegfaa的表达。我们提供的证据表明,后脑神经元不是vegfaa的来源,相反,受限制的pax6a +神经祖细胞(NPCs)指导中央动脉(CtAs)进入后脑。因此,MT3作为一个整合因子,为CtAs及时进入后脑提供必要的调节信号。