MCT1-mediated endothelial cell lactate shuttle as a target for promoting axon regeneration after spinal cord injury

被引:1
作者
Shi, Chaoran [1 ,2 ,3 ]
Xu, Jiaqi [1 ,2 ,3 ]
Ding, Yinghe [1 ,2 ,3 ]
Chen, Xingyi [4 ]
Yuan, Feifei [1 ,2 ,3 ]
Zhu, Fengzhang [1 ,2 ,3 ]
Duan, Chunyue [1 ,2 ,3 ]
Hu, Jianzhong [1 ,2 ,3 ]
Lu, Hongbin [2 ,3 ,5 ]
Wu, Tianding [1 ,2 ,3 ]
Jiang, Liyuan [1 ,2 ,3 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Spine Surg & Orthopaed, Changsha 410008, Hunan, Peoples R China
[2] Key Lab Organ Injury Aging & Regenerat Med Hunan P, Changsha 410008, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha 410008, Hunan, Peoples R China
[4] Cent South Univ, Xiangya Hosp, Eye Ctr, Changsha 410008, Hunan, Peoples R China
[5] Cent South Univ, Xiangya Hosp, Dept Sports Med, Changsha 410008, Hunan, Peoples R China
来源
THERANOSTICS | 2024年 / 14卷 / 14期
基金
中国国家自然科学基金;
关键词
spinal cord injury; endothelial cell; lactate shuttle; neuron metabolism; axon regeneration; TRAUMATIC BRAIN-INJURY; FUNCTIONAL RECOVERY; GENE-EXPRESSION; METABOLISM; TRANSPORT;
D O I
10.7150/thno.96374
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Rationale: Spinal cord injury (SCI)-induced vascular damage causes ischemia and hypoxia at the injury site, which, in turn, leads to profound metabolic disruptions. The effects of these metabolic alterations on neural tissue remodeling and functional recovery have yet to be elucidated. The current study aimed to investigate the consequences of the SCI-induced hypoxic environment at the epicenter of the injury. Methods: This study employed metabolomics to assess changes in energy metabolism after SCI. The use of a lactate sensor identified lactate shuttle between endothelial cells (ECs) and neurons. Reanalysis of single-cell RNA sequencing data demonstrated reduced MCT1 expression in ECs after SCI. Additionally, an adeno-associated virus (AAV) overexpressing MCT1 was utilized to elucidate its role in endothelial-neuronal interactions, tissue repair, and functional recovery. Results: The findings revealed markedly decreased monocarboxylate transporter 1 (MCT1) expression that facilitates lactate delivery to neurons to support their energy metabolism in ECs post-SCI. This decreased expression of MCT1 disrupts lactate transport to neurons, resulting in a metabolic imbalance that impedes axonal regeneration. Strikingly, our results suggested that administering adeno-associated virus specifically to ECs to restore MCT1 expression enhances axonal regeneration and improves functional recovery in SCI mice. These findings indicate a novel link between lactate shuttling from endothelial cells to neurons following SCI and subsequent neural functional recovery. Conclusion: In summary, the current study highlights a novel metabolic pathway for therapeutic interventions in the treatment of SCI. Additionally, our findings indicate the potential benefits of targeting lactate transport mechanisms in recovery from SCI.
引用
收藏
页码:5662 / 5681
页数:20
相关论文
共 50 条
  • [1] Epigenetic Regulation of Sensory Axon Regeneration after Spinal Cord Injury
    Finelli, Mattea J.
    Wong, Jamie K.
    Zou, Hongyan
    JOURNAL OF NEUROSCIENCE, 2013, 33 (50) : 19664 - 19676
  • [2] Regeneration of descending axon tracts after spinal cord injury
    Deumens, R
    Koopmans, GC
    Joosten, EAJ
    PROGRESS IN NEUROBIOLOGY, 2005, 77 (1-2) : 57 - 89
  • [3] Animal models of axon regeneration after spinal cord injury
    Lee, Do-Hun
    Lee, Jae K.
    NEUROSCIENCE BULLETIN, 2013, 29 (04) : 436 - 444
  • [4] Intrinsic regulation of axon regeneration after spinal cord injury: Recent advances and remaining challenges
    Noristani, Harun Najib
    EXPERIMENTAL NEUROLOGY, 2022, 357
  • [5] AAV-MEDIATED GENE THERAPY FOR AXON REGENERATION AFTER SPINAL CORD INJURY.
    Jendelova, Pavla
    TISSUE ENGINEERING PART A, 2023, 29 (11-12) : 840 - 840
  • [6] Stem Cell Strategies in Promoting Neuronal Regeneration after Spinal Cord Injury: A Systematic Review
    Bonosi, Lapo
    Silven, Manikon Poullay
    Biancardino, Antonio Alessandro
    Sciortino, Andrea
    Giammalva, Giuseppe Roberto
    Scerrati, Alba
    Sturiale, Carmelo Lucio
    Albanese, Alessio
    Tumbiolo, Silvana
    Visocchi, Massimiliano
    Iacopino, Domenico Gerardo
    Maugeri, Rosario
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (21)
  • [7] The role of RhoA in retrograde neuronal death and axon regeneration after spinal cord injury
    Hu, Jianli
    Zhang, Guixin
    Rodemer, William
    Jin, Li-Qing
    Shifman, Michael
    Selzer, Michael E.
    NEUROBIOLOGY OF DISEASE, 2017, 98 : 25 - 35
  • [8] Autophagy induction stabilizes microtubules and promotes axon regeneration after spinal cord injury
    He, Miao
    Ding, Yuetong
    Chu, Chen
    Tang, Jing
    Xiao, Qi
    Luo, Zhen-Ge
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (40) : 11324 - 11329
  • [9] Extrinsic and Intrinsic Regulation of Axon Regeneration by MicroRNAs after Spinal Cord Injury
    Li, Ping
    Teng, Zhao-Qian
    Liu, Chang-Mei
    NEURAL PLASTICITY, 2016, 2016
  • [10] Axon regeneration and exercise-dependent plasticity after spinal cord injury
    Houle, John D.
    Cote, Marie-Pascale
    NEURONS, CIRCUITRY, AND PLASTICITY IN THE SPINAL CORD AND BRAINSTEM, 2013, 1279 : 154 - 163