Intravenously Delivered Lipid Nanoparticles Access Acute Spinal Cord Injury via Disrupted Vasculature

Insights

Intravenously delivered mRNA-lipid nanoparticles can cross the disrupted blood-spinal cord barrier after spinal cord injury, enabling local gene expression in injured spinal cord cells.

Area of Science:

  • Neuroscience
  • Biotechnology
  • Regenerative Medicine

Background:

  • Spinal cord injury causes secondary damage via inflammation and cell death.
  • Current therapies face challenges like short half-lives and invasive delivery.
  • Messenger RNA (mRNA)-lipid nanoparticles offer transient protein production for potential therapies.

Purpose of the Study:

  • To determine if intravenous mRNA-lipid nanoparticles can target the injured spinal cord.
  • To investigate if these nanoparticles can leverage blood-spinal cord barrier disruption for local gene expression.

Main Methods:

  • Rats with spinal cord injury received intravenous reporter mRNA-lipid nanoparticles.
  • Transgene expression was quantified in the spinal cord and peripheral organs.
  • Expression was analyzed in various cell types (astrocytes, oligodendrocytes, microglia, neurons).

Main Results:

  • Intravenous delivery within 6 hours post-injury led to local transgene expression in the injured spinal cord.
  • mRNA-lipid nanoparticles successfully crossed the disrupted blood-spinal cord barrier.
  • Transgene expression was detected in multiple cell types within 3 hours and lasted up to 5 days.

Conclusions:

  • Systemic delivery of mRNA-lipid nanoparticles can exploit transient blood-spinal cord barrier disruption.
  • This strategy enables local gene expression within the injured spinal cord.
  • This approach holds promise for future spinal cord injury therapeutics.