Communicating pain: emerging axonal signaling in peripheral neuropathic pain

被引:1
|
作者
Testa, Livia [1 ,2 ]
Dotta, Sofia [1 ,2 ]
Vercelli, Alessandro [1 ,2 ]
Marvaldi, Letizia [1 ,2 ]
机构
[1] Neurosci Inst Cavalieri Ottolenghi Orbassano Torin, Turin, Italy
[2] Dept Neurosci Rita Levi Montalcini, Turin, Italy
来源
FRONTIERS IN NEUROANATOMY | 2024年 / 18卷
关键词
neuropathic pain; peripheral nerve injury; neurogenetics; axonal signaling; dorsal root ganglia; axonal regeneration; nerve regeneration; DORSAL-ROOT GANGLION; NERVE GROWTH-FACTOR; SENSORY NEURON SUBTYPES; SCHWANN-CELLS; CONGENITAL INSENSITIVITY; SCIATIC-NERVE; RETROGRADE TRANSPORT; LOCAL TRANSLATION; SEX-DIFFERENCES; RISK-FACTORS;
D O I
10.3389/fnana.2024.1398400
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Peripheral nerve damage often leads to the onset of neuropathic pain (NeuP). This condition afflicts millions of people, significantly burdening healthcare systems and putting strain on families' financial well-being. Here, we will focus on the role of peripheral sensory neurons, specifically the Dorsal Root Ganglia neurons (DRG neurons) in the development of NeuP. After axotomy, DRG neurons activate regenerative signals of axons-soma communication to promote a gene program that activates an axonal branching and elongation processes. The results of a neuronal morphological cytoskeleton change are not always associated with functional recovery. Moreover, any axonal miss-targeting may contribute to NeuP development. In this review, we will explore the epidemiology of NeuP and its molecular causes at the level of the peripheral nervous system and the target organs, with major focus on the neuronal cross-talk between intrinsic and extrinsic factors. Specifically, we will describe how failures in the neuronal regenerative program can exacerbate NeuP.
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收藏
页数:16
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