The
investigation of the effects of electrical and mechanical stimulations
on chondrogenesis in tissue engineering scaffolds is essential for
realizing successful cartilage repair and regeneration. The aim of
articular cartilage tissue engineering is to enhance the function
of damaged or diseased articular cartilage, which has limited regenerative
capacity. Studies have shown that electrical stimulation (ES) promotes
mesenchymal stem cell (MSC) chondrogenesis, while mechanical stimulation
(MS) enhances the chondrogenic differentiation capacity of MSCs. Therefore,
understanding the impact of these stimuli on chondrogenesis is crucial
for researchers to develop more effective tissue engineering strategies
for cartilage repair and regeneration. This study focuses on the preparation
of poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS)
conductive polymer (CP) scaffolds using the freeze-drying method.
The scaffolds were fabricated with varying concentrations (0, 1, 3,
and 10 wt %) of (3-glycidyloxypropyl) trimethoxysilane (GOPS) as a
crosslinker and an additive to tailor the scaffold properties. To
gain a comprehensive understanding of the material characteristics
and the phase aggregation phenomenon of PEDOT:PSS scaffolds, the researchers
performed theoretical calculations of solubility parameters and surface
energies of PSS, PSS-GOPS, and PEDOT polymers, as well as conducted
material analyses. Additionally, the study investigated the potential
of promoting chondrogenic differentiation of human adipose stem cells
by applying external ES or MS on a PEDOT:PSS CP scaffold. Compared
to the group without stimulation, the group that underwent stimulation
exhibited significantly up-regulated expression levels of chondrogenic
characteristic genes, such as SOX9 and COL2A1. Moreover, the immunofluorescence
staining images exhibited a more vigorous fluorescence intensity of
SOX9 and COL II proteins that was consistent with the trend of the
gene expression results. In the MS experiment, the strain excitation
exerted on the scaffold was simulated and transformed into stress.
The simulated stress response showed that the peak gradually decreased
with time and approached a constant value, with the negative value
of stress representing the generation of tensile stress. This stress
response quantification could aid researchers in determining specific
MS conditions for various materials in tissue engineering, and the
applied stress conditions could be further optimized. Overall, these
findings are significant contributions to future research on cartilage
repair and biophysical ES/MS in tissue engineering.