Azimi Ehsan, Reddy Vemuri B, Pereira Paula Juliana Seadi, Talbot Sebastien, Woolf Clifford J, Lerner Ethan A
Cutaneous Biology Research Center, Department of Dermatology, Massachusetts General Hospital and Harvard Medical School, Charlestown, Mass.
Cutaneous Biology Research Center, Department of Dermatology, Massachusetts General Hospital and Harvard Medical School, Charlestown, Mass; PUCRS, Programa de Pós-graduação em Biologia Celular e Molecular, Porto Alegre, Brazil.
J Allergy Clin Immunol. 2017 Aug;140(2):447-453.e3. doi: 10.1016/j.jaci.2016.12.980. Epub 2017 Feb 20.
Substance P (SP) is linked to itch and inflammation through activation of receptors on mast cells and sensory neurons. There is increasing evidence that SP functions through Mas-related G protein-coupled receptors (Mrgprs) in addition to its conventional receptor, neurokinin-1.
Because Mrgprs mediate some aspects of inflammation that had been considered mediated by neurokinin-1 receptor (NK-1R), we sought to determine whether itch induced by SP can also be mediated by Mrgprs.
Genetic and pharmacologic approaches were used to evaluate the contribution of Mrgprs to SP-induced scratching behavior and activation of cultured dorsal root ganglion neurons from mice.
SP-induced scratching behavior and activation of cultured dorsal root ganglion neurons was dependent on Mrgprs rather than NK-1R.
We deduce that SP activates MrgprA1 on sensory neurons rather than NK-1R to induce itch.
P物质(SP)通过激活肥大细胞和感觉神经元上的受体与瘙痒和炎症相关联。越来越多的证据表明,除了其传统受体神经激肽-1外,SP还通过Mas相关G蛋白偶联受体(Mrgprs)发挥作用。
由于Mrgprs介导了一些曾被认为由神经激肽-1受体(NK-1R)介导的炎症方面,我们试图确定SP诱导的瘙痒是否也可由Mrgprs介导。
采用遗传学和药理学方法评估Mrgprs对SP诱导的搔抓行为以及对培养的小鼠背根神经节神经元激活的作用。
SP诱导的搔抓行为和培养的背根神经节神经元的激活依赖于Mrgprs而非NK-1R。
我们推断SP激活感觉神经元上的MrgprA1而非NK-1R来诱导瘙痒。