Bandoła Joanna, Richter Cornelia, Ryser Martin, Jamal Arshad, Ashton Michelle P, von Bonin Malte, Kuhn Matthias, Dorschner Benjamin, Alexopoulou Dimitra, Navratiel Katrin, Roeder Ingo, Dahl Andreas, Hedrich Christian M, Bonifacio Ezio, Brenner Sebastian, Thieme Sebastian
Department of Pediatrics, University Clinic Dresden, Dresden, Germany.
Department of Medical Laboratory Sciences, Imperial College of Business Studies, Lahore, Pakistan.
Front Immunol. 2017 Aug 17;8:981. doi: 10.3389/fimmu.2017.00981. eCollection 2017.
Plasmacytoid dendritic cells (pDCs) regulate innate and adaptive immunity. Neurotrophins and their receptors control the function of neuronal tissue. In addition, they have been demonstrated to be part of the immune response but little is known about the effector immune cells involved. We report, for the first time, the expression and immune-regulatory function of the low affinity neurotrophin receptor p75 neurotrophin receptor (p75NTR) by the antigen-presenting pDCs, mediated by toll-like receptor (TLR) 9 activation and differential phosphorylation of interferon regulatory factor 3 and 7. The modulation of p75NTR on pDCs significantly influences disease progression of asthma in an ovalbumin-induced mouse model mediated by the TLR9 signaling pathway. p75NTR activation of pDCs from patients with asthma increased allergen-specific T cell proliferation and cytokine secretion in nerve growth factor concentration-dependent manner. Further, p75NTR activation of pDCs delayed the onset of autoimmune diabetes in RIP-CD80GP mice and aggravated graft-versus-host disease in a xenotransplantation model. Thus, p75NTR signaling on pDCs constitutes a new and critical mechanism connecting neurotrophin signaling and immune response regulation with great therapeutic potential for a variety of immune disorders.
浆细胞样树突状细胞(pDCs)调节先天性免疫和适应性免疫。神经营养因子及其受体控制神经组织的功能。此外,它们已被证明是免疫反应的一部分,但对其中涉及的效应免疫细胞知之甚少。我们首次报道了抗原呈递pDCs表达低亲和力神经营养因子受体p75神经营养因子受体(p75NTR)及其免疫调节功能,这是由Toll样受体(TLR)9激活以及干扰素调节因子3和7的差异磷酸化介导的。在卵清蛋白诱导的小鼠模型中,pDCs上p75NTR的调节通过TLR9信号通路显著影响哮喘的疾病进展。哮喘患者pDCs的p75NTR激活以神经生长因子浓度依赖性方式增加了过敏原特异性T细胞增殖和细胞因子分泌。此外,pDCs的p75NTR激活延迟了RIP-CD80GP小鼠自身免疫性糖尿病的发病,并在异种移植模型中加重了移植物抗宿主病。因此,pDCs上的p75NTR信号构成了一种新的关键机制,将神经营养因子信号与免疫反应调节联系起来,对多种免疫疾病具有巨大的治疗潜力。