神经元CCL2对高血糖作出反应,并在糖尿病背景下导致焦虑症。
Neuronal CCL2 responds to hyperglycaemia and contributes to anxiety disorders in the context of diabetes.
作者信息
Pan Kaijun, Gao Yanan, Zong Haichao, Zhang Yongmei, Qi Yingbei, Wang Hanlin, Chen Wengang, Zhou Ting, Zhao Jinwen, Yin Tao, Guo Haoran, Wang Min, Wang Hanmin, Pang Tao, Zang Yi, Li Jia
机构信息
Metabolic Disease Research Center, Jiangsu Key Laboratory of Drug Screening, China Pharmaceutical University, Nanjing, China.
State Key Laboratory of Chemical Biology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
出版信息
Nat Metab. 2025 May 6. doi: 10.1038/s42255-025-01281-2.
Anxiety disorders are frequently observed in patients with diabetes and can be associated with several diabetes-related factors. Here we determine that hyperglycaemia is a major cause for the development of anxiety disorders through a C-C motif chemokine ligand 2 (CCL2)-dependent mechanism. By adopting complementary strategies, we demonstrate that neuron-specific (not peripheral) CCL2 mediates anxiety-like behaviours in streptozotocin-induced diabetic mice. Mechanistically, high glucose levels induce Tonicity-responsive enhancer-binding protein (TonEBP)-dependent CCL2 expression in neurons, leading to microglial activation in a paracrine manner. Similar phenotypes are also observed in high-fat diet-induced diabetic mice, independent of insulin signalling. Furthermore, we reveal that neuronal CCL2 in the medial prefrontal cortex and ventral hippocampus synergistically induces anxiety-like behaviours, indicating brain region-specific effects on diabetic mice. Finally, we confirm that the neuronal TonEBP-CCL2 axis and inflammatory pathways are both upregulated in patients with diabetes. Conclusively, neuronal CCL2 is specifically increased by hyperglycaemia and contributes to anxiety disorders, providing additional insights into the link between diabetes and mental health disorders.
焦虑症在糖尿病患者中很常见,并且可能与多种糖尿病相关因素有关。在此,我们确定高血糖是通过C-C基序趋化因子配体2(CCL2)依赖性机制导致焦虑症发生的主要原因。通过采用互补策略,我们证明神经元特异性(而非外周)CCL2介导链脲佐菌素诱导的糖尿病小鼠的焦虑样行为。机制上,高血糖水平诱导神经元中渗透压反应增强子结合蛋白(TonEBP)依赖性CCL2表达,以旁分泌方式导致小胶质细胞活化。在高脂饮食诱导的糖尿病小鼠中也观察到类似表型,且与胰岛素信号无关。此外,我们发现内侧前额叶皮质和腹侧海马中的神经元CCL2协同诱导焦虑样行为,表明对糖尿病小鼠存在脑区特异性影响。最后,我们证实糖尿病患者神经元中的TonEBP-CCL2轴和炎症途径均上调。总之,高血糖特异性增加神经元CCL2并导致焦虑症,为糖尿病与精神健康障碍之间的联系提供了新的见解。