Ming-Chen Wang

Proteomic Profiling of Neuroblastoma Cells Adhesion on Hyaluronic Acid-Based Surface for Neural Tissue Engineering

The microenvironment of neuron cells plays a crucial role in regulating neural development and regeneration. Hyaluronic acid (HA) biomaterial has been applied in a wide range of medical and biological fields and plays important roles in neural regeneration. PC12 cells have been reported to be capable of endogenous NGF synthesis and secretion. The purpose of this research was to assess the effect of HA biomaterial combining with PC12 cells conditioned media (PC12 CM) in neural regeneration. Using SH-SY5Y cells as an experimental model, we found that supporting with PC12 CM enhanced HA function in SH-SY5Y cell proliferation and adhesion. Through RP-nano-UPLC-ESI-MS/MS analyses, we identified increased expression of HSP60 and RanBP2 in SH-SY5Y cells grown on HA-modified surface with cotreatment of PC12 CM. Moreover, we also identified factors that were secreted from PC12 cells and may promote SH-SY5Y cell proliferation and adhesion. Here, we proposed a biomaterial surface enriched with neurotrophic factors for nerve regeneration application.

Microcontact printing pattern as a mask for chemical etching: A scanning photoelectron microscopy study

Synchrotron-based scanning photoelectron spectromicroscopy and microspectroscopy were used to monitor the outcome of the etching process involving the transfer of a lithographic pattern produced by microcontact printing (μCP) of self-assembled monolayers (SAMs) to the underlying metal (gold) substrate. As a test system, octadecanethiolate (ODT) SAMs on gold substrates were chosen. The μCP ODT SAMs were found to protect the underlying gold against the wet-chemical etching, ensuring the effective transfer of the μCP pattern to the substrate. These SAMs exhibited only a slight degradation upon their exposure to the Au-etching solution. In contrast, a significant degradation of the edges of the printed features was observed. This degradation was predominantly related to a lateral diffusion of the active etching agents across these edges, along the SAMs-Au interface. This process can result in a blurring and narrowing of the printing features of a μCP SAM pattern at its transfer to the underlying substrate.