Decellularized
peripheral nerve matrix hydrogel (DNM-G) has drawn
increasing attention in the field of neural tissue engineering, owing
to its high tissue-specific bioactivity, drug/cell delivery capability,
and multifunctional processability. However, the mechanisms and influencing
factors of DNM-G formation have been rarely reported. To enable potential
biological applications, the relationship between gelation conditions
(including digestion time and gel concentration) and mechanical properties/stability
(sol–gel transition temperature, gelation time, nanotopology,
and storage modulus) of the DNM-G were systematically investigated
in this study. The adequate-digested decellularized nerve matrix solution
exhibited higher mechanical property, shorter gelation time, and
a lower gelation temperature. A noteworthy increase of β-sheet
proportion was identified through Fourier-transform infrared spectroscopy
(FTIR) and circular dichroism (CD) characterizations, which suggested
the possible major secondary structure formation during the phase
transition. Besides, the DNM-G degraded fast that over 70% mass loss
was noted after 4 weeks when immersing in PBS. A natural cross-linking
agent, genipin, was gently introduced into DNM-G to enhance its mechanical
properties and stability without changing its microstructure and biological
performance. As a prefabricated scaffold, DNM-G remarkably increased
the length and penetration depth of dorsal root ganglion (DRG) neurites
compared to collagen gel. Furthermore, the DNM-G promoted the myelination
and facilitated the formation of the morphological neural network.
Finally, we demonstrated the feasibility of applying DNM-G in support-free
extrusion-based 3D printing. Overall, the mechanical and biological
performance of DNM-G can be manipulated by tuning the processing parameters,
which is key to the versatile applications of DNM-G in regenerative
medicine.