Injury to the spinal cord results in paralysis below the level of the injury, and there are no current therapies that are able to restore function. Limited regeneration occurs as result of the local environment, which is deficient in stimulatory factors and has an excess of inhibitory factors. Our long-term goal is to develop multi-functional biomaterials that bridge the injury site to control the microenvironment to promote and direct axonal growth into and through, and to re-enter the host tissue to form functional connections with intact circuitry. In the initial funding period, we have developed multiple channel bridges that mechanically stabilize the injury site that limits secondary damage, and promotes axonal growth into and across the injury, with axonal re-entry into the host tissue. Additionally, we have an unparalleled ability to localize delivery of gene therapy vectors, with which expression of neurotrophic factors significantly enhanced the number of regenerating axons. Having established a system that supports axonal growth through the injury and into the host tissue, we now focus on forming functional connections of these regenerating axons with intact circuitry of the spinal cord. Thus, the objectives of this proposal are to i) myelinate the regenerating axons provide the appropriate conduction speed of neural impulses, ii) enhance axonal re-entry into the host tissue, and iii) extension of the re-entering axons to healthy tissue for connection with intact circuitry. The initial step towards these objectives is to regulate the inflammatory response, which normally initiates a cascade of events leading to secondary tissue damage, including neural and glial death, and production of chondroitin sulfate proteoglycans (CS), a major component of the glial scar. Inflammation will be targeted by the bridge architecture (Aim 1a), as cell infiltration differs between the channels and pores of the bridge. Additionally, our gene delivery transducers macrophages, and we will investigate strategies to promote a more regenerative phenotype (M2) rather than a more inflammatory phenotype (M1) (Aim 1b). Reducing inflammation is expected to increase survival of neurons and glial, which should enhance the number of regenerating fibers and enhance myelination. Subsequently, we propose to employ shRNA to target the inhibitory components of the glial scar (Aim 2), which is deposited at the interface between the bridge and host tissue. Preventing deposition of these inhibitory components is anticipated to enhance the number of axons re-entering host tissue. Finally, nanoparticle based gene delivery will be employed to create gradients caudal to the bridge and promote extension of axons that have re-entered the host tissue, which can enable connections with intact circuitry (Aim 3). These controllable systems can identify the design necessary for the formation of functional connections. Additionally, these systems have well-defined components that have been used in the clinic, which may facilitate the ultimate translation to the clinic.
Injury to the spinal cord results in paralysis below the level of the injury, and current therapeutic strategies are ineffective at restoring function. The spinal cord has the intrinsic potential to regenerate, but does not due to the insufficient supply of growth promoting factors and an excess of inhibitory factors. We are developing biomaterials capable of gene delivery as a means to control the environment at the spinal cord. This proposal focuses on using these tools to reduce the presence of inhibitory factors within the injury, and to provide a gradient of growth factors that will direct axons to leave the biomaterials and re-enter the host tissue and form functional connections. Controllable systems such as this will identify the contribution of each component to functional outcome, and can be tuned to obtain the functionality necessary for translation to the clinic.
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|Thomas, Aline M; Gomez, Andrew J; Palma, Jaime L et al. (2014) Heparin-chitosan nanoparticle functionalization of porous poly(ethylene glycol) hydrogels for localized lentivirus delivery of angiogenic factors. Biomaterials 35:8687-93|
|Tuinstra, Hannah M; Margul, Daniel J; Goodman, Ashley G et al. (2014) Long-term characterization of axon regeneration and matrix changes using multiple channel bridges for spinal cord regeneration. Tissue Eng Part A 20:1027-37|
|Thomas, Aline M; Seidlits, Stephanie K; Goodman, Ashley G et al. (2014) Sonic hedgehog and neurotrophin-3 increase oligodendrocyte numbers and myelination after spinal cord injury. Integr Biol (Camb) 6:694-705|
|Thomas, Aline M; Shea, Lonnie D (2014) Cryotemplation for the Rapid Fabrication of Porous, Patternable Photopolymerized Hydrogels. J Mater Chem B Mater Biol Med 2:4521-4530|
|Gower, R Michael; Boehler, Ryan M; Azarin, Samira M et al. (2014) Modulation of leukocyte infiltration and phenotype in microporous tissue engineering scaffolds via vector induced IL-10 expression. Biomaterials 35:2024-31|
|Thomas, Aline M; Shea, Lonnie D (2013) Polysaccharide-modified scaffolds for controlled lentivirus delivery in vitro and after spinal cord injury. J Control Release 170:421-9|
|Seidlits, Stephanie K; Gower, Robert Michael; Shepard, Jaclyn A et al. (2013) Hydrogels for lentiviral gene delivery. Expert Opin Drug Deliv 10:499-509|
|Tuinstra, Hannah M; Ducommun, Melissa M; Briley, William E et al. (2013) Gene delivery to overcome astrocyte inhibition of axonal growth: an in vitro model of the glial scar. Biotechnol Bioeng 110:947-57|
|Thomas, Aline M; Kubilius, Matthew B; Holland, Samantha J et al. (2013) Channel density and porosity of degradable bridging scaffolds on axon growth after spinal injury. Biomaterials 34:2213-20|
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