| Literature DB >> 33592210 |
Audra A Kramer1, Greta M Olson2, Advaita Chakraborty3, Murray G Blackmore4.
Abstract
Axons in the corticospinal tract (CST) display a limited capacity for compensatory sprouting after partial spinal injuries, potentially limiting functional recovery. Forced expression of a developmentally expressed transcription factor, Krüppel-like factor 6 (KLF6), enhances axon sprouting by adult CST neurons. Here, using a pyramidotomy model of injury in adult mice, we confirm KLF6's pro-sprouting properties in spared corticospinal tract neurons and show that this effect depends on an injury stimulus. In addition, we probed the time course of KLF6-triggered sprouting of CST axons and demonstrate a significant enhancement of growth within four weeks of treatment. Finally, we tested whether KLF6-induced sprouting was accompanied by improvements in forelimb function, either singly or when combined with intensive rehabilitation. We found that regardless of rehabilitative training, and despite robust cross-midline sprouting by corticospinal tract axons, treatment with KLF6 produced no significant improvement in forelimb function on either a modified ladder-crossing task or a pellet-retrieval task. These data clarify important details of KLF6's pro-growth properties and indicate that additional interventions or further optimization will be needed to translate this improvement in axon growth into functional gains.Entities:
Keywords: Axon regeneration; Corticospinal tract; Gene therapy; Pyramidotomy; Rehabilitation; Spinal cord injury
Mesh:
Substances:
Year: 2021 PMID: 33592210 PMCID: PMC8224817 DOI: 10.1016/j.expneurol.2021.113644
Source DB: PubMed Journal: Exp Neurol ISSN: 0014-4886 Impact factor: 5.330