Chara Simitzi graduated as a Chemical Engineer from the National Technical University of Athens (Greece) and then continued her studies in biomedical and tissue engineering
. She pursued her MSc in Biomedical Engineering from RWTH Aachen University (Germany); PhD in Biology from University of Crete (Greece). After her PhD she worked at the Foundation for Research and Technology - Hellas Institute in Crete and the Queen Mary University of London (UK) respectively. She is currently a Postdoctoral Research Associate in the group of Professor Day (Applied Biomedical Engineering
group) at the University College London. Her scientific interests focus on the cell biomaterial interface
and more specifically on the development of novel types of scaffolds for tissue engineering applications and cell culture platforms for in vitro studies to address cell biology
Statement of the Problem
: Mesenchymal stem cells (MSCs)
are becoming increasingly important due to the broad spectrum of trophic and immunomodulatory factors they secrete. The MSC secretome
plays a role in angiogenesis and revascularization
, immune modulation and tissue repair
; however, there is a lack of methods suitable for controlling this effect. Evidence exists to show cell substrates influence MSC behaviour. Therefore, manipulating the cell substrate could provide improved methods for controlling the secretome for new therapies but there is currently a lack of cell substrates
suitable for implantation.
and cultured for 16 days in xeno-free medium. Cell growth on the microparticles was evaluated at different time-points and compared with cells cultured on tissue culture plastic
. The angiogenic activity of the ADMSC secretome was evaluated by ELISA
and in vitro angiogenesis assays.
: Three different types of TIPS microparticles with different morphological and physicochemical characteristics were investigated. ADMSCs adhered and proliferated on all types of the microparticles. Vascular endothelial growth factor (VEGF)
secretion was increased from cells cultured on the microparticles compared with cells cultured on tissue culture plastic. MSCs attached to microparticles remained viable after 16 days, were capable of migrating from the microparticles, and retained their lineage plasticity