» Articles » PMID: 37443728

Regenerative Potential of Injured Spinal Cord in the Light of Epigenetic Regulation and Modulation

Overview
Journal Cells
Publisher MDPI
Date 2023 Jul 14
PMID 37443728
Authors
Affiliations
Soon will be listed here.
Abstract

A spinal cord injury is a form of physical harm imposed on the spinal cord that causes disability and, in many cases, leads to permanent mammalian paralysis, which causes a disastrous global issue. Because of its non-regenerative aspect, restoring the spinal cord's role remains one of the most daunting tasks. By comparison, the remarkable regenerative ability of some regeneration-competent species, such as some Urodeles (Axolotl), , and some teleost fishes, enables maximum functional recovery, even after complete spinal cord transection. During the last two decades of intensive research, significant progress has been made in understanding both regenerative cells' origins and the molecular signaling mechanisms underlying the regeneration and reconstruction of damaged spinal cords in regenerating organisms and mammals, respectively. Epigenetic control has gradually moved into the center stage of this research field, which has been helped by comprehensive work demonstrating that DNA methylation, histone modifications, and microRNAs are important for the regeneration of the spinal cord. In this review, we concentrate primarily on providing a comparison of the epigenetic mechanisms in spinal cord injuries between non-regenerating and regenerating species. In addition, we further discuss the epigenetic mediators that underlie the development of a regeneration-permissive environment following injury in regeneration-competent animals and how such mediators may be implicated in optimizing treatment outcomes for spinal cord injurie in higher-order mammals. Finally, we briefly discuss the role of extracellular vesicles (EVs) in the context of spinal cord injury and their potential as targets for therapeutic intervention.

Citing Articles

Neurons Are Not All the Same: Diversity in Neuronal Populations and Their Intrinsic Responses to Spinal Cord Injury.

Siebert J, Kennedy K, Osterhout D ASN Neuro. 2025; 17(1):2440299.

PMID: 39819292 PMC: 11877619. DOI: 10.1080/17590914.2024.2440299.


Nature's Secret Neuro-Regeneration Pathway in Axolotls, Polychaetes and Planarians for Human Therapeutic Target Pathways.

Mansor N, Balqis T, Lani M, Lye K, Nor Muhammad N, Ismail W Int J Mol Sci. 2024; 25(22).

PMID: 39595973 PMC: 11593954. DOI: 10.3390/ijms252211904.


Immunomodulation of Cancer Cells Using Autologous Blood Concentrates as a Patient-Specific Cell Culture System: A Comparative Study on Osteosarcoma and Fibrosarcoma Cell Lines.

Dohle E, Parkhoo K, Bennardo F, Schmeinck L, Sader R, Ghanaati S Bioengineering (Basel). 2024; 11(4).

PMID: 38671725 PMC: 11048113. DOI: 10.3390/bioengineering11040303.


Post-Traumatic Expressions of Aromatase B, Glutamine Synthetase, and Cystathionine-Beta-Synthase in the Cerebellum of Juvenile Chum Salmon, .

Pushchina E, Bykova M, Varaksin A Int J Mol Sci. 2024; 25(6).

PMID: 38542274 PMC: 10970380. DOI: 10.3390/ijms25063299.


The Protein Acetylation after Traumatic Spinal Cord Injury: Mechanisms and Therapeutic Opportunities.

Li H, Zhang H Int J Med Sci. 2024; 21(4):725-731.

PMID: 38464830 PMC: 10920853. DOI: 10.7150/ijms.92222.


References
1.
Hayta E, Elden H . Acute spinal cord injury: A review of pathophysiology and potential of non-steroidal anti-inflammatory drugs for pharmacological intervention. J Chem Neuroanat. 2017; 87:25-31. DOI: 10.1016/j.jchemneu.2017.08.001. View

2.
Tran A, Warren P, Silver J . New insights into glial scar formation after spinal cord injury. Cell Tissue Res. 2021; 387(3):319-336. PMC: 8975767. DOI: 10.1007/s00441-021-03477-w. View

3.
Ujigo S, Kamei N, Hadoush H, Fujioka Y, Miyaki S, Nakasa T . Administration of microRNA-210 promotes spinal cord regeneration in mice. Spine (Phila Pa 1976). 2014; 39(14):1099-107. DOI: 10.1097/BRS.0000000000000356. View

4.
Finelli M, Wong J, Zou H . Epigenetic regulation of sensory axon regeneration after spinal cord injury. J Neurosci. 2013; 33(50):19664-76. PMC: 3858634. DOI: 10.1523/JNEUROSCI.0589-13.2013. View

5.
Kouzarides T . Chromatin modifications and their function. Cell. 2007; 128(4):693-705. DOI: 10.1016/j.cell.2007.02.005. View