Author/Authors :
Qin Liu، نويسنده , , Zongxiang Tang، نويسنده , , Lenka Surdenikova، نويسنده , , Seungil Kim، نويسنده , , Kush N. Patel، نويسنده , , Andrew Kim، نويسنده , , Fei Ru، نويسنده , , Yun Guan، نويسنده , , Hao-Jui Weng، نويسنده , , Yixun Geng، نويسنده , , Bradley J. Undem، نويسنده , , Marian Kollarik، نويسنده , , Zhou-Feng Chen، نويسنده , , David J. Anderson، نويسنده , , Xinzhong Dong، نويسنده ,
Abstract :
The cellular and molecular mechanisms mediating histamine-independent itch in primary sensory neurons are largely unknown. Itch induced by chloroquine (CQ) is a common side effect of this widely used antimalarial drug. Here, we show that Mrgprs, a family of G protein-coupled receptors expressed exclusively in peripheral sensory neurons, function as itch receptors. Mice lacking a cluster of Mrgpr genes display significant deficits in itch induced by CQ but not histamine. CQ directly excites sensory neurons in an Mrgpr-dependent manner. CQ specifically activates mouse MrgprA3 and human MrgprX1. Loss- and gain-of-function studies demonstrate that MrgprA3 is required for CQ responsiveness in mice. Furthermore, MrgprA3-expressing neurons respond to histamine and coexpress gastrin-releasing peptide, a peptide involved in itch sensation, and MrgprC11. Activation of these neurons with the MrgprC11-specific agonist BAM8-22 induces itch in wild-type but not mutant mice. Therefore, Mrgprs may provide molecular access to itch-selective neurons and constitute novel targets for itch therapeutics.