Nguyen Thanh Khoa, Baker Sophia, Angtuaco Julienne, Arceri Liana, Kaczor Samuel, Fitzsimonds Bram, Hawkins Matthew R, Wingert Rebecca A
Department of Biological Sciences, Center for Stem Cells and Regenerative Medicine, Center for Zebrafish Research, University of Notre Dame, Notre Dame, IN 46556, USA.
J Dev Biol. 2025 Jun 17;13(2):20. doi: 10.3390/jdb13020020.
Endocannabinoid signaling plays a significant role in neurogenesis and nervous system physiology, but its roles in the development of other tissues are just beginning to be appreciated. Previous reports have shown the presence of the key endocannabinoid receptor Cannabinoid receptor 1 (CB1 or Cnr1) in multiciliated (MCC) tissues and its upregulation in kidney diseases, yet the relationship between Cnr1 and renal MCC development is unknown. Here, we report that Cnr1 is essential for cilia development across tissues and regulates renal MCCs via cyclic AMP (cAMP) signaling during zebrafish embryogenesis. Using a combination of genetic and pharmacological studies, we found that the loss of function, agonism and antagonism of all lead to reduced mature renal MCC populations. deficiency also led to reduced cilia development across tissues, including the pronephros, ear, Kupffer's vesicle (KV), and nasal placode. Interestingly, treatment with the cAMP activator Forskolin (FSK) restored renal MCC defects in agonist-treated embryos, suggesting that mediates cAMP signaling in renal MCC development. Meanwhile, treatment with the cAMP inhibitor SQ-22536 alone or with deficiency led to reduced MCC populations, suggesting that also mediates renal MCC development independently of cAMP signaling. Our findings indicate that has a critical role in controlling renal MCC development both via cAMP signaling and an independent pathway, further revealing implications for ciliopathies and renal diseases.
内源性大麻素信号传导在神经发生和神经系统生理学中发挥着重要作用,但其在其他组织发育中的作用才刚刚开始被认识到。先前的报道显示,关键的内源性大麻素受体大麻素受体1(CB1或Cnr1)存在于多纤毛(MCC)组织中,并且在肾脏疾病中上调,然而Cnr1与肾MCC发育之间的关系尚不清楚。在这里,我们报告Cnr1对于跨组织的纤毛发育至关重要,并在斑马鱼胚胎发育过程中通过环磷酸腺苷(cAMP)信号传导调节肾MCC。通过遗传和药理学研究的结合,我们发现功能丧失、激动和拮抗均导致成熟肾MCC群体减少。缺乏也导致跨组织的纤毛发育减少,包括前肾、耳、库普弗小泡(KV)和鼻基板。有趣的是,用cAMP激活剂福斯高林(FSK)处理可恢复激动剂处理胚胎中的肾MCC缺陷,表明在肾MCC发育中介导cAMP信号传导。同时,单独使用cAMP抑制剂SQ-22536或与缺乏一起处理导致MCC群体减少,表明也独立于cAMP信号传导介导肾MCC发育。我们的研究结果表明,在通过cAMP信号传导和独立途径控制肾MCC发育方面具有关键作用,进一步揭示了对纤毛病和肾脏疾病的影响。