Department of Physiology, Yonsei University Wonju College of Medicine, Wonju 26426, Republic of Korea.
Mitohormesis Research Center, Yonsei University Wonju College of Medicine, Wonju 26426, Republic of Korea.
Cells. 2024 Jun 4;13(11):978. doi: 10.3390/cells13110978.
Precise control of neuronal activity is crucial for the proper functioning of neurons. How lipid homeostasis contributes to neuronal activity and how much of it is regulated by cells autonomously is unclear. In this study, we discovered that absence of the lipid regulator , a functional ortholog of the peroxisome proliferator-activated receptor (PPAR) in , resulted in defective pathogen avoidance behavior against (PA14). Functional NHR-49 was required in the neurons, and more specifically, in a set of oxygen-sensing body cavity neurons, URX, AQR, and PQR. We found that lowering the neuronal activity of the body cavity neurons improved avoidance in mutants. Calcium imaging in URX neurons showed that mutants displayed longer-lasting calcium transients in response to an O upshift, suggesting that excess neuronal activity leads to avoidance defects. Cell-specific rescue of NHR-49 in the body cavity neurons was sufficient to improve pathogen avoidance, as well as URX neuron calcium kinetics. Supplementation with oleic acid also improved avoidance behavior and URX calcium kinetics, suggesting that the defective calcium response in the neuron is due to lipid dysfunction. These findings highlight the role of cell-autonomous lipid regulation in neuronal physiology and immune behavior.
精确控制神经元活动对于神经元的正常功能至关重要。脂稳态如何促进神经元活动,以及细胞自主调节的程度如何,目前还不清楚。在这项研究中,我们发现,缺失脂质调节剂 ,一种在 中过氧化物酶体增殖物激活受体 (PPAR)的功能同源物,导致对 (PA14)的病原体回避行为缺陷。神经元中需要功能性 NHR-49,更具体地说,需要在一组氧感应体腔神经元 URX、AQR 和 PQR 中。我们发现,降低体腔神经元的神经元活性可以改善 突变体的回避行为。URX 神经元的钙成像显示, 突变体对 O 上移的钙瞬变持续时间更长,表明过度的神经元活动导致回避缺陷。在体腔神经元中特异性拯救 NHR-49 足以改善病原体回避以及 URX 神经元钙动力学。补充油酸也可以改善回避行为和 URX 钙动力学,表明神经元中钙反应的缺陷是由于脂质功能障碍。这些发现强调了细胞自主脂质调节在神经元生理学和免疫行为中的作用。