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Comparative analysis of aligned and random amniotic membrane-derived cryogels for neural tissue repair. | LitMetric

Comparative analysis of aligned and random amniotic membrane-derived cryogels for neural tissue repair.

Biomater Sci

TEMA - Centre for Mechanical Technology and Automation, Department of Mechanical Engineering, University of Aveiro, 3810-193, Aveiro, Portugal.

Published: August 2024

AI Article Synopsis

  • The study focuses on a new method to enhance neural regeneration by using protein-derived cryogels with aligned pores from the human amniotic membrane, which can help restore the geometry of neural tissue.
  • Aligned cryogels support better proliferation and differentiation of neural stem cells (NSC), leading to more extensive cell infiltration, neurite extension, and overall cellular growth compared to randomly structured cryogels.
  • The presence of functional synaptic connections in the aligned cryogels highlights the importance of scaffold microstructure in promoting effective neuronal reconnection and healing.

Article Abstract

The ordered arrangement of cells and extracellular matrix facilitates the seamless transmission of electrical signals along axons in the spinal cord and peripheral nerves. Therefore, restoring tissue geometry is crucial for neural regeneration. This study presents a novel method using proteins derived from the human amniotic membrane, which is modified with photoresponsive groups, to produce cryogels with aligned porosity. Freeze-casting was used to produce cryogels with longitudinally aligned pores, while cryogels with randomly distributed porosity were used as the control. The cryogels exhibited remarkable injectability and shape-recovery properties, essential for minimally invasive applications. Different tendencies in proliferation and differentiation were evident between aligned and random cryogels, underscoring the significance of the scaffold's microstructure in directing the behaviour of neural stem cells (NSC). Remarkably, aligned cryogels facilitated extensive cellular infiltration and migration, contrasting with NSC cultured on isotropic cryogels, which predominantly remained on the scaffold's surface throughout the proliferation experiment. Significantly, the proliferation assay demonstrated that on day 7, the aligned cryogels contained eight times more cells compared to the random cryogels. Consistent with the proliferation experiments, NSC exhibited the ability to differentiate into neurons within the aligned scaffolds and extend neurites longitudinally. In addition, differentiation assays showed a four-fold increase in the expression of neural markers in the cross-sections of the aligned cryogels. Conversely, the random cryogels exhibited minimal presence of cell bodies and extensions. The presence of synaptic vesicles on the anisotropic cryogels indicates the formation of functional synaptic connections, emphasizing the importance of the scaffold's microstructure in guiding neuronal reconnection.

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Source
http://dx.doi.org/10.1039/d4bm00364kDOI Listing

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