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Matching mechanical heterogeneity of the native spinal cord augments axon infiltration in 3D-printed scaffolds.
Tran, Kiet A; DeOre, Brandon J; Ikejiani, David; Means, Kristen; Paone, Louis S; De Marchi, Laura; Suprewicz, Lukasz; Koziol, Katarina; Bouyer, Julien; Byfield, Fitzroy J; Jin, Ying; Georges, Penelope; Fischer, Itzhak; Janmey, Paul A; Galie, Peter A.
Afiliación
  • Tran KA; Department of Biomedical Engineering, Rowan University, Glassboro, NJ, USA.
  • DeOre BJ; Department of Biomedical Engineering, Rowan University, Glassboro, NJ, USA.
  • Ikejiani D; Department of Bioengineering, Rice University, Houston, TX, USA.
  • Means K; Department of Bioengineering, Rice University, Houston, TX, USA.
  • Paone LS; Department of Biomedical Engineering, Rowan University, Glassboro, NJ, USA.
  • De Marchi L; Department of Biomedical Engineering, Rowan University, Glassboro, NJ, USA.
  • Suprewicz L; Department of Medical Microbiology and Nanobiomedical Engineering, Medical University of Bialystok, Bialystok, Poland.
  • Koziol K; Department of Biomedical Engineering, Rowan University, Glassboro, NJ, USA.
  • Bouyer J; Department of Neurobiology and Anatomy, Drexel College of Medicine, Philadelphia, PA, USA.
  • Byfield FJ; Department of Physiology, University of Pennsylvania, Philadelphia, PA, USA.
  • Jin Y; Department of Neurobiology and Anatomy, Drexel College of Medicine, Philadelphia, PA, USA.
  • Georges P; Council on Science and Technology, Princeton University, Princeton, NJ, USA.
  • Fischer I; Department of Neurobiology and Anatomy, Drexel College of Medicine, Philadelphia, PA, USA.
  • Janmey PA; Department of Physiology, University of Pennsylvania, Philadelphia, PA, USA.
  • Galie PA; Department of Biomedical Engineering, Rowan University, Glassboro, NJ, USA. Electronic address: galie@rowan.edu.
Biomaterials ; 295: 122061, 2023 04.
Article en En | MEDLINE | ID: mdl-36842339
Scaffolds delivered to injured spinal cords to stimulate axon connectivity often match the anisotropy of native tissue using guidance cues along the rostral-caudal axis, but current approaches do not mimic the heterogeneity of host tissue mechanics. Although white and gray matter have different mechanical properties, it remains unclear whether tissue mechanics also vary along the length of the cord. Mechanical testing performed in this study indicates that bulk spinal cord mechanics do differ along anatomical level and that these differences are caused by variations in the ratio of white and gray matter. These results suggest that scaffolds recreating the heterogeneity of spinal cord tissue mechanics must account for the disparity between gray and white matter. Digital light processing (DLP) provides a means to mimic spinal cord topology, but has previously been limited to printing homogeneous mechanical properties. We describe a means to modify DLP to print scaffolds that mimic spinal cord mechanical heterogeneity caused by variation in the ratio of white and gray matter, which improves axon infiltration compared to controls exhibiting homogeneous mechanical properties. These results demonstrate that scaffolds matching the mechanical heterogeneity of white and gray matter improve the effectiveness of biomaterials transplanted within the injured spinal cord.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Traumatismos de la Médula Espinal Límite: Humans Idioma: En Revista: Biomaterials Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Traumatismos de la Médula Espinal Límite: Humans Idioma: En Revista: Biomaterials Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos