The Physicochemical Properties of Decellularized Extracellular Matrix-Coated 3D Printed Poly(ε-caprolactone) Nerve Conduits for Promoting Schwann Cells Proliferation and Differentiation.
Chung-Chia ChenJoyce YuHooi-Yee NgAlvin Kai-Xing LeeChien-Chang ChenYueh-Sheng ChenMing-You ShiePublished in: Materials (Basel, Switzerland) (2018)
Although autologous nerve grafting remains the gold standard treatment for peripheral nerve injuries, alternative methods such as development of nerve guidance conduits have since emerged and evolved to counter the many disadvantages of nerve grafting. However, the efficacy and viability of current nerve conduits remain unclear in clinical trials. Here, we focused on a novel decellularized extracellular matrix (dECM) and polydopamine (PDA)-coated 3D-printed poly(ε-caprolactone) (PCL)-based conduits, whereby the PDA surface modification acts as an attachment platform for further dECM attachment. We demonstrated that dECM/PDA-coated PCL conduits possessed higher mechanical properties when compared to human or animal nerves. Such modifications were proved to affect cell behaviors. Cellular behaviors and neuronal differentiation of Schwann cells were assessed to determine for the efficacies of the conduits. There were some cell-specific neuronal markers, such as Nestin, neuron-specific class III beta-tubulin (TUJ-1), and microtubule-associated protein 2 (MAP2) analyzed by enzyme-linked immunosorbent assay, and Nestin expressions were found to be 0.65-fold up-regulated, while TUJ1 expressions were 2.3-fold up-regulated and MAP2 expressions were 2.5-fold up-regulated when compared to Ctl. The methodology of PDA coating employed in this study can be used as a simple model to immobilize dECM onto PCL conduits, and the results showed that dECM/PDA-coated PCL conduits can as a practical and clinically viable tool for promoting regenerative outcomes in larger peripheral nerve defects.
Keyphrases
- peripheral nerve
- extracellular matrix
- induced apoptosis
- cell therapy
- clinical trial
- transcription factor
- stem cells
- single cell
- cell cycle arrest
- endothelial cells
- high throughput
- mesenchymal stem cells
- signaling pathway
- endoplasmic reticulum stress
- type diabetes
- brain injury
- cell death
- adipose tissue
- high density
- study protocol
- cell proliferation
- weight loss
- open label
- double blind
- lactic acid
- pi k akt
- glycemic control