Lysophosphatidic Acid Receptors LPAR5 and LPAR2 Inversely Control Hydroxychloroquine-Evoked Itch and Scratching in Mice

• Published in: International journal of molecular sciences 2024-08, Vol.25 (15), p.8177
• Main Authors: Fischer, Caroline, Schreiber, Yannick, Nitsch, Robert, Vogt, Johannes, Thomas, Dominique, Geisslinger, Gerd, Tegeder, Irmgard
• Format: Article
• Language: English
• Subjects: Animals; autotaxin; dorsal root ganglia; G proteins; Ganglia, Spinal - drug effects; Ganglia, Spinal - metabolism; Gene expression; Histamine; Histology; Hydroxychloroquine - pharmacology; itch; Kinases; Localization; lysophosphatidic acid; Lysophospholipids - metabolism; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Neurons; Neuropeptides; Peptides; Phosphatase; Phosphoric Diester Hydrolases - genetics; Phosphoric Diester Hydrolases - metabolism; plasticity related gene 1; Proteins; pruritus; Pruritus - chemically induced; Pruritus - drug therapy; Pruritus - genetics; Pruritus - metabolism; Receptors, Lysophosphatidic Acid - genetics; Receptors, Lysophosphatidic Acid - metabolism; Signal Transduction - drug effects; Spinal cord
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25158177

Lysophosphatidic acids (LPAs) evoke nociception and itch in mice and humans. In this study, we assessed the signaling paths. Hydroxychloroquine was injected intradermally to evoke itch in mice, which evoked an increase of LPAs in the skin and in the thalamus, suggesting that peripheral and central LPA receptors (LPARs) were involved in HCQ-evoked pruriception. To unravel the signaling paths, we assessed the localization of candidate genes and itching behavior in knockout models addressing LPAR5, LPAR2, autotaxin/ENPP2 and the lysophospholipid phosphatases, as well as the plasticity-related genes Prg1/LPPR4 and Prg2/LPPR3. LacZ reporter studies and RNAscope revealed LPAR5 in neurons of the dorsal root ganglia (DRGs) and in skin keratinocytes, LPAR2 in cortical and thalamic neurons, and Prg1 in neuronal structures of the dorsal horn, thalamus and SSC. HCQ-evoked scratching behavior was reduced in sensory neuron-specific Advillin-LPAR5 mice (peripheral) but increased in LPAR2 and Prg1 mice (central), and it was not affected by deficiency of glial autotaxin (GFAP-ENPP2 ) or Prg2 (PRG2 ). Heat and mechanical nociception were not affected by any of the genotypes. The behavior suggested that HCQ-mediated itch involves the activation of peripheral LPAR5, which was supported by reduced itch upon treatment with an LPAR5 antagonist and autotaxin inhibitor. Further, HCQ-evoked calcium fluxes were reduced in primary sensory neurons of Advillin-LPAR5 mice. The results suggest that LPA-mediated itch is primarily mediated via peripheral LPAR5, suggesting that a topical LPAR5 blocker might suppress "non-histaminergic" itch.