Abstract

<p indent="0mm">Interneurons are the main local loop connecting sensory and motor neurons and play an important role in the pathological changes after spinal cord injury and the corresponding repair process. After spinal cord injury, astrocyte proliferation and glial scar formation are the main factors hindering the effective regeneration and growth of injured spinal cord axons. In the early stage of neurogenesis, neuroepithelial cells produce astrocytes and intermediate neurons. Therefore, it is likely that astrocytes and intermediate neurons arise from common progenitor cells. In the spinal cord, neuron and glial cell differentiation is regulated by a transcription factor network. In particular, Nkx6.1 is critical for the fate determination of progenitor cells into ventral interneurons. However, the role of Nkx6.1 in the birth of spinal astrocytes after spinal cord injury is still unclear. Herein, we first used the Cre-LoxP system and Rosa26 gene knock-in technology to specifically induce an <italic>Nkx6</italic>.<italic>1</italic> knockout and introduce a lycopene marker gene in different neural precursor cells of adult mice’s spinal cord. Next, we constructed a knockout spinal cord injury model and performed immunofluorescence staining. The staining results showed a substantial number of Nkx6.1<sup>+</sup> cells in the injured area after spinal cord injury, while <italic>Nkx6</italic>.<italic>1</italic> ablation one week after spinal cord injury would hinder the formation of the glial scar and inhibit the production of En1<sup>+</sup> intermediate neurons by regulating the expression pattern of Pax6<italic> </italic>in the central neural tube. In conclusion, our study shows that <italic>Nkx6</italic>.<italic>1</italic> plays a crucial role in spinal cord injury, being responsible for effective axon regeneration and motor function recovery.

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