Locomotor recovery after spinal cord injury: intimate dependence between axonal regeneration and re-connection

Hector Ramiro Quintá

Traumatic spinal cord injuries (SCI) are characterized by damage in the integrity of the spinal cord, which results in either temporary or permanent alterations in the locomotor, sensory and/or autonomic functions (Yezierski, 2009).The traumatic event leads to impairments in voluntary control of movement below the injury by affecting the connection between the brain and the neurons localized in the spinal cord.Therefore, the recovery of locomotor activity is considered one of the main goals in the search of new therapies by the scientists around the world.For many years, axon regeneration has been considered the Holy Grail in SCI research, however, now we know that the regeneration of sectioned axons is necessary but not enough to promote locomotor recovery (Raineteau and Schwab, 2001).The disruption of long motor and sensory axonal tracts as a consequence of the lesion prevents their specific interactions with their cellular targets.For this reason the goal of ongoing investigations is to promote the re-growth of axonal tracts across the lesion site and their re-connection with propiospinal neurons at different segments of the spinal cord (Figure 1A).In particular, regeneration and re-connection of corticospinal tract (CST) axons is of vital significance to regain voluntary locomotor activity after a complete spinal cord injury(Оudega and Perez, 2012).This is because the axons that integrate the CST transmit voluntary motor information to the forelimbs and hindlimbs, and the damage of this structure in humans affects directly the locomotion (Nathan, 1994).

At the cellular level, an intrinsic neuronal mechanism has been described, where cortical neurons activate a regenerative program in response to injury.This cellular mechanism reflects an attempt to restore the loss of function; however this self-recovery mechanism is completely inefficient.Taking into account this premise, researchers around the world are working on the development of biological therapies to heal the lesioned spinal cord.For example, several approaches target the cytoskeleton of damaged axons,enhancing the re-polimerization of actin,tubulin and neurofilaments and preventing the production of oxidative species that contribute to the degenerative process(Ruschel et al., 2015; Quinta et al., 2016).Оther approaches act on the metabolism and energy balance of neurons, restoring cellular energy, in particular enhancing the mitocondrial transport to promote axonal regeneration and synaptic re-connection(Han et al., 2020).However, axonal regrowth after SCI does not ensure a proper guidance and navigation of regenerated axons across the lesion site, and synaptic re-connection with their specific neuronal effectors.

To address this limitation, in a recent study I examined the effect of Netrin-1 treatment on axonal regeneration across the lesion, and synaptic re-connection to re-establish locomotion after SCI (Quinta,2021).

Netrin-1 is a developmental axon guidance cue involved in CST growth, CST 3-dimensional navigation, and neuronal connection.In particular, this molecule regulates the degree of decussation of the CST at the medulla oblongata (Meneret et al., 2017).The mechanism involves two major Netrin-1 receptors, known as UNC5h and DCC (Deleted in Colorectal Cancer), which could act as trigger of repulsive or attractive signaling during development (Keino-Masu et al., 1996).

The therapeutic effect of Netrin-1 was addressed using a rat model of complete spinal cord transection (T10–11).This model is suitable to investigate axonal regeneration after SCI, since the precision of the lesion causes minimal tissue loss but severs all axons, disconnecting spinal circuits below the injury site from all supra-spinal input, as well as all ascending axons.

This study showed that Netrin-1 administered at the time of injury in the epicenter of the lesion, promotes a significant regeneration of axonal tracts localized at the white matter segment across the transected area [Figure 4 from Quinta (2021)].In particular regrown CST axons were identified by three-dimnesional imaging on cleared whole spinal cord.It was also shown that regenerated axons that crossed the lesion presented trans-synaptic interactions with their targets below the injury.This interaction between regenerated axons and their neuronal targets in the spinal cord prevented the trans-synaptic degeneration of spinal neurons.This effect was reflected in the preservation of axonal structures in peripheral nerves, like the sciatic nerve.Finally, rats treated with Netrin-1 after complete SCI recovered their locomotion, in contrast to what was observed in vehicle-treated injured rats[Figure 1 from Quinta (2021)].

Figure 1｜Corticospinal tract regeneration after SCI.

The locomotor recovery observed is dependent on the regeneration of ascendant/descendent axons across the lesion and their re-connection with specific neuronal targets, rather than due to a compensatory response below the lesion site triggered by spinal circuit plasticity.To confirm this, rats treated with Netrin-1 after SCI were re-transected in the same anatomical location.As a consequence,rats showed a complete paralysis of the hindlims.This result confirmed that the recovery of locomotion was the result of the regeneration of axonal tracts across the lesion and their re-connection with spinal neurons.

The complete molecular mechanism by which acute Netrin-1 administration promotes locomotor recovery is far from being elucidated yet.We know that after SCI, Netrin-1 is expressed by neurons and oligodendrocytes that are surrounding the lesion.However, in the epicenter of the lesion, a sharp decrease in the level of Netrin-1 is observed in both neurons and oligodendrocytes.These low levels of Netrin-1 persist at least 7 months after SCI (Manitt et al., 2006).In line with this,a recent research shows that cortical neurons attempt to activate a regenerative transcriptomic program after SCI(Poplawski et al., 2020).This regenerative state is defined by the up-regulation of several genes involved in cellular growth,and the down-regulation of growthinhibitory pathways.Interesting in the context of this perspective, bothNTN1gene and its receptor UNC5b are upregulated after injury.Therefore, the effect of exogenous Netrin-1 administration could mimic this transcriptional program,promoting an embryonic regenerative state.Moreover, exogenous Netrin-1 addition also could prevent the sharp drop in Netrin-1 levels at the epicenter of the lesion.Together, these two effects could overcome the low efficiency of spontaneous re-growth, improving the regeneration process.

Evidence shows that the molecular pathway of axonal regeneration could involve extracellular calcium influx in response to Netrin-1/Netrin-1 receptors interaction, since this molecular mediator participates in the actin and tubulin cytoskeleton assembly in the growth cone(Figure 1B).Therefore the future work will be oriented to identify the mechanism by which this mediator interacts with voltagegated calcium and/or TRP channels in response to Netrin-1 treatment.

Finally, the biological approaches where the restorative mechanisms involve the regrowth of axons after a mechanical lesion could be useful in other neuropathologies where axonal trauma takes place as well.For example traumatic brain injury or peripheral nerve injuries, could be excellent models to explore new potential applications in the future since both require the regeneration of the axonal shaft.

Hector Ramiro Quintá*

Consejo Nacional de Investigaciones Científicas y Técnicas, CОNICET; Laboratorio de Medicina Experimental “Dr.Jorge E.Toblli”, Hospital Alemán,Buenos Aires, Argentina

*Correspondence to:Héctor Ramiro Quintá, PhD,quintaramiro@gmail.com.

https://orcid.org/0000-0002-2098-7346(Hector Ramiro Quintá)

Date of submission:March 17, 2021

Date of decision:April 27, 2021

Date of acceptance:June 3, 2021

Date of web publication:August 4, 2021

https://doi.org/10.4103/1673-5374.320977

How to cite this article:Quintá HR (2022)Locomotor recovery after spinal cord injury:intimate dependence between axonal regeneration and re-connection.Neural Regen Res 17(3):553-554.

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Peer review:Externally peer reviewed.

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Open peer reviewer:David Romeo-Guitart,Universitat Autònoma de Barcelona, Spain.

Additional file:Open peer review report 1.