Matching mechanical heterogeneity of the native spinal cord augments axon infiltration in 3D-printed scaffolds

被引:10
|
作者
Tran, Kiet A. [1 ]
DeOre, Brandon J. [1 ]
Ikejiani, David [2 ]
Means, Kristen [2 ]
Paone, Louis S. [1 ]
De Marchi, Laura [1 ]
Suprewicz, Lukasz [3 ]
Koziol, Katarina [1 ]
Bouyer, Julien [4 ]
Byfield, Fitzroy J. [5 ]
Jin, Ying [4 ]
Georges, Penelope [6 ]
Fischer, Itzhak [4 ]
Janmey, Paul A. [5 ]
Galie, Peter A. [1 ]
机构
[1] Rowan Univ, Dept Biomed Engn, Glassboro, NJ 08028 USA
[2] Rice Univ, Dept Bioengn, Houston, TX USA
[3] Med Univ Bialystok, Dept Med Microbiol & Nanobiomed Engn, Bialystok, Poland
[4] Drexel Coll Med, Dept Neurobiol & Anat, Philadelphia, PA USA
[5] Univ Penn, Dept Physiol, Philadelphia, PA USA
[6] Princeton Univ, Council Sci & Technol, Princeton, NJ USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Digital light processing; Rheology; Spinal cord injury; Axon regeneration; Tissue engineering; 3D-printing; CENTRAL-NERVOUS-SYSTEM; IN-VITRO; GRAY-MATTER; STEM-CELL; HYDROGEL; TISSUE; GROWTH; INJURY; DIFFERENTIATION; DUROTAXIS;
D O I
10.1016/j.biomaterials.2023.122061
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
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页数:12
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