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多功能工程蛋白 C2C 靶向外周感觉神经元的细胞内 G-肌动蛋白,缓解炎症性疼痛。

Intracellular G-actin targeting of peripheral sensory neurons by the multifunctional engineered protein C2C confers relief from inflammatory pain.

机构信息

School of Biological Sciences, University of Nebraska, E234 Beadle Center, Lincoln, NE, 68588, USA.

Center for Biotechnology, University of Nebraska, E234 Beadle Center, Lincoln, NE, 68588, USA.

出版信息

Sci Rep. 2020 Jul 30;10(1):12789. doi: 10.1038/s41598-020-69612-9.

Abstract

The engineered multifunctional protein C2C was tested for control of sensory neuron activity by targeted G-actin modification. C2C consists of the heptameric oligomer, C2II-CI, and the monomeric ribosylase, C2I. C2C treatment of sensory neurons and SH-SY5Y cells in vitro remodeled actin and reduced calcium influx in a reversible manner. C2C prepared using fluorescently labeled C2I showed selective in vitro C2I delivery to primary sensory neurons but not motor neurons. Delivery was dependent on presence of both C2C subunits and blocked by receptor competition. Immunohistochemistry of mice treated subcutaneously with C2C showed colocalization of subunit C2I with CGRP-positive sensory neurons and fibers but not with ChAT-positive motor neurons and fibers. The significance of sensory neuron targeting was pursued subsequently by testing C2C activity in the formalin inflammatory mouse pain model. Subcutaneous C2C administration reduced pain-like behaviors by 90% relative to untreated controls 6 h post treatment and similarly to the opioid buprenorphene. C2C effects were dose dependent, equally potent in female and male animals and did not change gross motor function. One dose was effective in 2 h and lasted 1 week. Administration of C2I without C2II-CI did not reduce pain-like behavior indicating its intracellular delivery was required for behavioral effect.

摘要

工程化多功能蛋白 C2C 通过靶向 G-肌动蛋白修饰来测试对感觉神经元活性的控制。C2C 由七聚体寡聚物 C2II-CI 和单体核糖核酸酶 C2I 组成。C2C 处理体外感觉神经元和 SH-SY5Y 细胞可使肌动蛋白重塑并以可逆的方式减少钙内流。使用荧光标记的 C2I 制备的 C2C 显示对原代感觉神经元而非运动神经元的选择性体外 C2I 递呈。递呈依赖于 C2C 两个亚基的存在,并被受体竞争所阻断。用 C2C 皮下处理的小鼠的免疫组织化学显示亚基 C2I 与 CGRP 阳性感觉神经元和纤维共定位,但与 ChAT 阳性运动神经元和纤维不共定位。随后通过在福尔马林炎症性小鼠疼痛模型中测试 C2C 的活性来研究感觉神经元靶向的意义。与未处理的对照组相比,C2C 给药 6 小时后可使疼痛样行为减少 90%,与阿片类药物丁丙诺啡的效果相当。C2C 作用呈剂量依赖性,在雌性和雄性动物中同样有效,且不会改变大体运动功能。单次剂量在 2 小时内有效,持续 1 周。没有 C2II-CI 的 C2I 给药不会减轻疼痛样行为,表明其细胞内递呈对于行为效应是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b5/7393082/950e593f53ee/41598_2020_69612_Fig1_HTML.jpg

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