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Published on: December 31, 2017
Intravenously Delivered Lipid Nanoparticles Access Acute Spinal Cord Injury via Disrupted Vasculature
Abstract:
Trauma to the spinal cord disrupts the blood-spinal cord barrier and triggers a secondary injury cascade characterized by inflammation and progressive neuronal and glial cell death. Therapeutic cytokines and growth factors have shown promise as a treatment in preclinical studies, though their clinical translation is limited by short protein half-lives and the need for invasive intraspinal administration. Lipid nanoparticle-mediated delivery of mRNA offers an alternative strategy that enables transient protein production. Here, we investigated whether intravenously administered mRNA-lipid nanoparticles could leverage the injury-induced disruption of the blood-spinal cord barrier to access the injured spinal cord for local transgene expression. After spinal cord injury in a rat, lipid nanoparticles loaded with reporter mRNA were administered intravenously, and transgene expression was quantified in the spinal cord and peripheral organs. Intravenous delivery within a 6-hours post-injury resulted in local transgene expression in the injured spinal cord, demonstrating that mRNA-lipid nanoparticles cross the disrupted blood-spinal cord barrier. Transgene expression was observed in astrocytes, oligodendrocytes, microglia, and neurons, detected within 3 hours and remained elevated for up to 5 days post-injury. These findings demonstrate that systemic mRNA-lipid nanoparticles delivery exploit transient blood-spinal cord barrier disruption to achieve local gene expression in the injured spinal cord.
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.
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