Hanes William M, Olofsson Peder S, Talbot Sébastien, Tsaava Tea, Ochani Mahendar, Imperato Gavin H, Levine Yaakov A, Roth Jesse, Pascal Maud A, Foster Simmie L, Wang Ping, Woolf Clifford, Chavan Sangeeta S, Tracey Kevin J
Laboratory of Biomedical Science, The Feinstein Institute for Medical Research, Manhasset, New York, United States of America.
Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, United States of America.
Bioelectron Med. 2016;3:18-28. doi: 10.15424/bioelectronmed.2016.00001. Epub 2016 Dec 20.
When pathogens and toxins breech the epithelial barrier, antigens are transported by the lymphatic system to lymph nodes. In previously immunized animals, antigens become trapped in the draining lymph nodes, but the underlying mechanism that controls antigen restriction is poorly understood. Here we describe the role of neurons in sensing and restricting antigen flow in lymph nodes. The antigen keyhole-limpet hemocyanin (KLH) injected into the mouse hind paw flows from the popliteal lymph node to the sciatic lymph node, continuing through the upper lymphatics to reach the systemic circulation. Re-exposure to KLH in previously immunized mice leads to decreased flow from the popliteal to the sciatic lymph node as compared with naïve mice. Administering bupivacaine into the lymph node region restores antigen flow in immunized animals. In contrast, neural activation using magnetic stimulation significantly decreases antigen trafficking in naïve animals as compared with sham controls. Ablating Na1.8 + sensory neurons significantly reduces antigen restriction in immunized mice. Genetic deletion of FcγRI/FcεRI also reverses the antigen restriction. Colocalization of PGP9.5-expressing neurons, FcγRI receptors and labeled antigen occurs at the antigen challenge site. Together, these studies reveal that neuronal circuits modulate antigen trafficking through a pathway that requires Na1.8 and FcγR.
当病原体和毒素突破上皮屏障时,抗原会通过淋巴系统运输至淋巴结。在先前已免疫的动物中,抗原会滞留在引流淋巴结中,但控制抗原限制的潜在机制仍知之甚少。在此,我们描述了神经元在感知和限制淋巴结中抗原流动方面的作用。注入小鼠后爪的抗原钥孔血蓝蛋白(KLH)从腘淋巴结流向坐骨淋巴结,继续通过上部淋巴管到达体循环。与未免疫的小鼠相比,先前免疫的小鼠再次接触KLH会导致从腘淋巴结到坐骨淋巴结的流量减少。在淋巴结区域注射布比卡因可恢复免疫动物体内的抗原流动。相反,与假手术对照组相比,使用磁刺激激活神经会显著减少未免疫动物体内的抗原运输。切除Na1.8 +感觉神经元会显著降低免疫小鼠的抗原限制。FcγRI/FcεRI的基因缺失也会逆转抗原限制。表达PGP9.5的神经元、FcγRI受体和标记抗原在抗原攻击部位共定位。总之,这些研究表明,神经回路通过一条需要Na1.8和FcγR的途径调节抗原运输。