Chronic stress hinders sensory axon regeneration via impairing mitochondrial cristae and OXPHOS.
Yu RuanJin ChengJiafeng DaiZhengwen MaShiyu LuoRun YanLizhao WangJinrui ZhouBin YuXiao-Ping TongHong-Xing ShenLibing ZhouTi-Fei YuanQi HanPublished in: Science advances (2023)
Spinal cord injury (SCI) often leads to physical limitations, persistent pain, and major lifestyle shifts, enhancing the likelihood of prolonged psychological stress and associated disorders such as anxiety and depression. The mechanisms linking stress with regeneration remain elusive, despite understanding the detrimental impact of chronic stress on SCI recovery. In this study, we investigated the effect of chronic stress on primary sensory axon regeneration using a preconditioning lesions mouse model. Our data revealed that chronic stress-induced mitochondrial cristae loss and a decrease in oxidative phosphorylation (OXPHOS) within primary sensory neurons, impeding central axon regrowth. Corticosterone, a stress hormone, emerged as a pivotal player in this process, affecting satellite glial cells by reducing Kir4.1 expression. This led to increased neuronal hyperactivity and reactive oxygen species levels, which, in turn, deformed mitochondrial cristae and impaired OXPHOS, crucial for axonal regeneration. Our study underscores the need to manage psychological stress in patients with SCI for effective sensory-motor rehabilitation.
Keyphrases
- stress induced
- spinal cord injury
- stem cells
- mouse model
- oxidative stress
- neuropathic pain
- reactive oxygen species
- spinal cord
- induced apoptosis
- type diabetes
- metabolic syndrome
- chronic pain
- cell proliferation
- poor prognosis
- heat stress
- machine learning
- wound healing
- cell death
- drug induced
- electronic health record
- signaling pathway
- optical coherence tomography
- brain injury
- ischemia reperfusion injury
- long non coding rna
- sleep quality
- blood brain barrier
- single molecule
- big data