脊髄後角アストロサイトの活性化は、接触性皮膚炎モデルマウスにおいて痒み伝達を増強する

Chronic itch is a major symptom in various skin diseases, such as atopic and contact dermatitis, but its mechanism remains to be determined. We have previously shown that spinal dorsal horn (SDH) astrocytes become activated in mouse models of chronic itch and that astrocyte-derived lipocalin-2 (LCN2...

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Published in日本薬理学会年会要旨集 p. 1-YIA-05
Main Authors 古賀, 啓祐, 山方, 涼, 白鳥, 美穂, 津田, 誠
Format Journal Article
LanguageJapanese
Published 公益社団法人 日本薬理学会 2019
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Abstract Chronic itch is a major symptom in various skin diseases, such as atopic and contact dermatitis, but its mechanism remains to be determined. We have previously shown that spinal dorsal horn (SDH) astrocytes become activated in mouse models of chronic itch and that astrocyte-derived lipocalin-2 (LCN2) is crucial for maintaining chronic itching. However, how LCN2 enhances spinal itch neurotransmission is not understood. In this study, using Gastrin-releasing peptide receptor (Grpr)-egfp mice to label itch-specific neurons in SDH, we found GRP-induced depolarization of excitatory GRPR+ neurons was greatly potentiated in contact dermatitis model mice. Genetic inhibition of signal transducer and activator transcription 3 (STAT3) in SDH astrocytes ameliorated chronic itch and also normalized enhancement of GRP-induced depolarization of excitatory GRPR+ neurons in chronic itch model. Furthermore, coadministration of LCN2 and GRP also potentiated GRP-induced depolarization of excitatory GRPR+ neurons. Our finding indicate that reactive astrocytes facilitated SDH itch transmission in chronic itch via upregulated LCN2.
AbstractList Chronic itch is a major symptom in various skin diseases, such as atopic and contact dermatitis, but its mechanism remains to be determined. We have previously shown that spinal dorsal horn (SDH) astrocytes become activated in mouse models of chronic itch and that astrocyte-derived lipocalin-2 (LCN2) is crucial for maintaining chronic itching. However, how LCN2 enhances spinal itch neurotransmission is not understood. In this study, using Gastrin-releasing peptide receptor (Grpr)-egfp mice to label itch-specific neurons in SDH, we found GRP-induced depolarization of excitatory GRPR+ neurons was greatly potentiated in contact dermatitis model mice. Genetic inhibition of signal transducer and activator transcription 3 (STAT3) in SDH astrocytes ameliorated chronic itch and also normalized enhancement of GRP-induced depolarization of excitatory GRPR+ neurons in chronic itch model. Furthermore, coadministration of LCN2 and GRP also potentiated GRP-induced depolarization of excitatory GRPR+ neurons. Our finding indicate that reactive astrocytes facilitated SDH itch transmission in chronic itch via upregulated LCN2.
Author 津田, 誠
山方, 涼
白鳥, 美穂
古賀, 啓祐
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  fullname: 津田, 誠
  organization: 九州大・院薬・ライフイノベーション分野
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Snippet Chronic itch is a major symptom in various skin diseases, such as atopic and contact dermatitis, but its mechanism remains to be determined. We have previously...
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Title 脊髄後角アストロサイトの活性化は、接触性皮膚炎モデルマウスにおいて痒み伝達を増強する
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