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将触觉转化为痒觉的脊髓神经回路。

A spinal neural circuitry for converting touch to itch sensation.

机构信息

Center for the Study of Itch and Sensory Disorders, Washington University School of Medicine, St. Louis, MO, 63110, USA.

Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO, 63110, USA.

出版信息

Nat Commun. 2020 Oct 8;11(1):5074. doi: 10.1038/s41467-020-18895-7.

Abstract

Touch and itch sensations are crucial for evoking defensive and emotional responses, and light tactile touch may induce unpleasant itch sensations (mechanical itch or alloknesis). The neural substrate for touch-to-itch conversion in the spinal cord remains elusive. We report that spinal interneurons expressing Tachykinin 2-Cre (Tac2) receive direct Aβ low threshold mechanoreceptor (LTMR) input and form monosynaptic connections with GRPR neurons. Ablation or inhibition markedly reduces mechanical but not acute chemical itch nor noxious touch information. Chemogenetic inhibition of Tac2 neurons also displays pronounced deficit in chronic dry skin itch, a type of chemical itch in mice. Consistently, ablation of gastrin-releasing peptide receptor (GRPR) neurons, which are essential for transmitting chemical itch, also abolishes mechanical itch. Together, these results suggest that innocuous touch and chemical itch information converge on GRPR neurons and thus map an exquisite spinal circuitry hard-wired for converting innocuous touch to irritating itch.

摘要

触觉和瘙痒感对于引发防御和情绪反应至关重要,而轻微的触觉可能会引起不愉快的瘙痒感(机械性瘙痒或异触感)。脊髓中触觉到瘙痒感转换的神经基础仍难以捉摸。我们报告称,表达速激肽 2-Cre(Tac2)的脊髓中间神经元接收直接的 Aβ 低阈值机械感受器(LTMR)输入,并与 GRPR 神经元形成单突触连接。敲除或抑制 Tac2 神经元会显著减少机械性但不会减少急性化学性瘙痒感或伤害性触觉信息。化学遗传抑制 Tac2 神经元也会导致慢性干燥皮肤瘙痒(一种小鼠的化学性瘙痒)明显缺陷。一致地,胃泌素释放肽受体(GRPR)神经元的敲除(化学性瘙痒传递所必需的)也会消除机械性瘙痒感。总之,这些结果表明无害的触觉和化学性瘙痒信息汇聚到 GRPR 神经元,从而构建了一个用于将无害的触觉转化为刺激性瘙痒的精确的脊髓环路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9985/7545208/527d431a32d5/41467_2020_18895_Fig1_HTML.jpg

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