Department of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Department of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Cell Rep. 2024 Apr 23;43(4):114058. doi: 10.1016/j.celrep.2024.114058. Epub 2024 Apr 12.
Proteasomes are critical for peripheral nervous system (PNS) function. Here, we investigate mammalian PNS proteasomes and reveal the presence of the neuronal membrane proteasome (NMP). We show that specific inhibition of the NMP on distal nerve fibers innervating the mouse hind paw leads to reduction in mechanical and pain sensitivity. Through investigating PNS NMPs, we demonstrate their presence on the somata and proximal and distal axons of a subset of dorsal root ganglion (DRG) neurons. Single-cell RNA sequencing experiments reveal that the NMP-expressing DRGs are primarily MrgprA3 and Cysltr2. NMP inhibition in DRG cultures leads to cell-autonomous and non-cell-autonomous changes in Ca signaling induced by KCl depolarization, αβ-meATP, or the pruritogen histamine. Taken together, these data support a model whereby NMPs are expressed on a subset of somatosensory DRGs to modulate signaling between neurons of distinct sensory modalities and indicate the NMP as a potential target for controlling pain.
蛋白酶体对于周围神经系统 (PNS) 的功能至关重要。在这里,我们研究了哺乳动物的 PNS 蛋白酶体,并揭示了神经元膜蛋白酶体 (NMP) 的存在。我们发现,特异性抑制支配小鼠后爪的远端神经纤维上的 NMP 会导致机械和疼痛敏感性降低。通过研究 PNS NMP,我们证明它们存在于一组背根神经节 (DRG) 神经元的胞体以及近侧和远侧轴突上。单细胞 RNA 测序实验表明,表达 NMP 的 DRG 主要是 MrgprA3 和 Cysltr2。在 DRG 培养物中抑制 NMP 会导致由 KCl 去极化、αβ-meATP 或瘙痒原组胺诱导的 Ca 信号的细胞自主和非细胞自主变化。综上所述,这些数据支持这样一种模型,即 NMP 表达在一组感觉神经元 DRG 上,以调节不同感觉模态神经元之间的信号传递,并表明 NMP 是控制疼痛的潜在靶点。