Aligned hydrogel tubes guide regeneration following spinal cord injury

• Published in: Acta biomaterialia 2019-03, Vol.86, p.312-322
• Main Authors: Dumont, Courtney M., Carlson, Mitchell A., Munsell, Mary K., Ciciriello, Andrew J., Strnadova, Katerina, Park, Jonghyuck, Cummings, Brian J., Anderson, Aileen J., Shea, Lonnie D.
• Format: Article
• Language: English
• Subjects: Animals; Apposition; Axon elongation; Axon guidance; Axons; Axons - drug effects; Axons - pathology; Biomaterials; Biomedical materials; Cicatrix - pathology; Cross-Linking Reagents - chemistry; Female; Hindlimb - drug effects; Hindlimb - physiology; Hydrogels; Hydrogels - pharmacology; Immune system; Implantation; Infiltration; Injuries; Locomotion - drug effects; Maleimides - chemistry; Mechanical properties; Mice, Inbred C57BL; Microspheres; Modular biomaterial; Myelin Sheath - drug effects; Myelin Sheath - metabolism; Nerve Regeneration - drug effects; Neuroglia - pathology; Polyethylene Glycols - chemistry; Polymerization; Porosity; Recovery of function; Regeneration (physiology); Regenerative medicine; Robust control; Soft tissues; Spinal cord injuries; Spinal Cord Injuries - pathology; Spinal Cord Injuries - physiopathology; Spinal cord injury; Surgical implants; Tissue engineering; Tissue repair; Tissue Scaffolds - chemistry; Tubes
• ISSN: 1742-7061; 1878-7568
• DOI: 10.1016/j.actbio.2018.12.052

[Display omitted] Directing the organization of cells into a tissue with defined architectures is one use of biomaterials for regenerative medicine. To this end, hydrogels are widely investigated as they have mechanical properties similar to native soft tissues and can be formed in situ to conform to a defect. Herein, we describe the development of porous hydrogel tubes fabricated through a two-step polymerization process with an intermediate microsphere phase that provides macroscale porosity (66.5%) for cell infiltration. These tubes were investigated in a spinal cord injury model, with the tubes assembled to conform to the injury and to provide an orientation that guides axons through the injury. Implanted tubes had good apposition and were integrated with the host tissue due to cell infiltration, with a transient increase in immune cell infiltration at 1 week that resolved by 2 weeks post injury compared to a gelfoam control. The glial scar was significantly reduced relative to control, which enabled robust axon growth along the inner and outer surface of the tubes. Axon density within the hydrogel tubes (1744 axons/mm2) was significantly increased more than 3-fold compared to the control (456 axons/mm2), with approximately 30% of axons within the tube myelinated. Furthermore, implantation of hydrogel tubes enhanced functional recovery relative to control. This modular assembly of porous tubes to fill a defect and directionally orient tissue growth could be extended beyond spinal cord injury to other tissues, such as vascular or musculoskeletal tissue. Tissue engineering approaches that mimic the native architecture of healthy tissue are needed following injury. Traditionally, pre-molded scaffolds have been implemented but require a priori knowledge of wound geometries. Conversely, hydrogels can conform to any injury, but do not guide bi-directional regeneration. In this work, we investigate the feasibility of a system of modular hydrogel tubes to promote bi-directional regeneration after spinal cord injury. This system allows for tubes to be cut to size during surgery and implanted one-by-one to fill any injury, while providing bi-directional guidance. Moreover, this system of tubes can be broadly applied to tissue engineering approaches that require a modular guidance system, such as repair to vascular or musculoskeletal tissues.