School of Medicine, Tsinghua University, Beijing 100084, China.
State Key Laboratory of Membrane Biology, Peking University, Beijing 100871, China; School of Life Sciences, Peking University, Beijing 100871, China.
Cell Rep. 2019 Jun 25;27(13):3799-3807.e3. doi: 10.1016/j.celrep.2019.05.082.
The nervous system can modulate the body's immunity. However, how efferent neural signals reach out to control the local immunity remains incompletely understood. Here, we report the ImmuView procedure for whole-tissue 3D assessment of neural innervations in the intact immune organs of adult mice. This advanced imaging technique revealed an intricate, panicle-shaped sympathetic architecture in the parenchyma of the spleen but not other immune organs, including the lymph nodes, Peyer's patch, and thymus. In contrast, we observed the minimal presence of parasympathetic innervations in the parenchyma of all of the classic immune organs examined. Specific deletion of the TrkA receptor abolishes the sympathetic architecture in the spleen and such genetic ablation significantly enhanced the spleen antibacterial innate immunity. Moreover, the sympathetic neurotransmitter norepinephrine could inhibit the LPS-elicited innate immunity cell-intrinsically via β2-adrenergic receptor signaling. This study exemplifies the key link that specifically connects the efferent sympathetic signal with the spleen innate immunity.
神经系统可以调节身体的免疫力。然而,传出的神经信号如何到达并控制局部免疫仍不完全清楚。在这里,我们报告了 ImmuView 程序,用于对成年小鼠完整免疫器官中神经支配的整个组织进行 3D 评估。这项先进的成像技术揭示了脾脏实质中错综复杂的、呈球状的交感神经结构,但在其他免疫器官中没有发现,包括淋巴结、派尔氏斑和胸腺。相比之下,我们观察到所有经典免疫器官实质中副交感神经支配的存在极少。TrkA 受体的特异性缺失会破坏脾脏中的交感神经结构,这种基因缺失会显著增强脾脏的抗细菌固有免疫。此外,交感神经递质去甲肾上腺素可以通过β2-肾上腺素能受体信号内在地抑制 LPS 引发的固有免疫细胞。这项研究说明了一个关键的联系,即传出的交感信号与脾脏固有免疫之间的联系。