3D printable Sodium alginate-Matrigel (SA-MA) hydrogel facilitated ectomesenchymal stem cells (EMSCs) neuron differentiation.
Yang LiXia CaoWenwen DengQingtong YuCongyong SunPing MaFengxia ShaoMukhtar Mohammed YusifZhumei GeKaili WangRan LiJiangnan YuXi-Ming XuPublished in: Journal of biomaterials applications (2020)
Ectomesenchymal stem cells (EMSCs) are typical adult stem cells obtained from the cranial neural crest. They have the potential to differentiate into various cell types, such as osseous cells, neurons and glial cells. Three-dimensional (3 D) printing is a novel method to construct biological structures by rapid prototyping. Previously, our group reported on the stemness and multi-lineage differentiation potential of EMSCs on gels. However, the exploration of EMSCs in 3 D printing and then evaluation of the growth and neuronal differentiation of EMSCs on extruded 3 D printable hybrid hydrogels has not been reported. Therefore, the current study explored the novel hybrid Sodium alginate-Matrigel (SA-MA) hydrogel extruded 3 D printing to design an in vitro scaffold to promote the differentiation and growth of EMSCs. In addition, the physical properties of the hydrogel were characterized and its drug-releasing property determined. Notably, the results showed that the construct exhibited a sustain-released effect of growth factor BDNF in accordance with the Higuchi equation. Moreover, the cell survival rate on the 3 D printed scaffold was 88.22 ± 1.13% with higher neuronal differentiation efficiency compared with 2 D culture. Thus, SA-MA's ability to enhanced EMSCs neuronal differentiation offers a new biomaterial for neurons regeneration in the treatment of spinal cord injury.
Keyphrases
- stem cells
- tissue engineering
- growth factor
- wound healing
- drug delivery
- spinal cord injury
- induced apoptosis
- cell therapy
- spinal cord
- hyaluronic acid
- physical activity
- single cell
- emergency department
- high resolution
- oxidative stress
- endoplasmic reticulum stress
- risk assessment
- cell proliferation
- climate change
- cell death
- mass spectrometry
- blood brain barrier
- subarachnoid hemorrhage