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October 22-23, 2018 | Frankfurt, Germany

International Conference on

Robo t i c s a n d A u t oma t i o n

B iomater ial s and Nanomater ial s

Joint Event

&

Journal of Biomedical Research | Volume 29

The impact of intercellular communication in complex pre-vascularized tissue equivalents

Martin Heller

Johannes Gutenberg University Mainz, Germany

A

promising approach in reconstructive surgery for the

wound coverage after surgical interventions is the use of

artificially generated pre-vascularized tissue equivalents. In

our group we developed a pre-vascularized buccal mucosa

equivalent in a tri-culture of primary buccal epithelial cells,

fibroblasts and microvascular endothelial cells successfully,

based on the collagen matrix Bio-Gide® from Geistlich. A

successful pre-vascularization at superficial areas of the

matrix was demonstrated. However, so far the generation of

pre-vascularized structures within the tissue equivalent was

restricted to only superficial areas of the matrix. Besides the

great advances, it is not completely understood yet, why the

used endothelial cells did not migrate in depth of the tissue

equivalent in order to form vascular structures. To understand

the cell biological background for the reduced migration

willingness of endothelial cells, we investigated the intercellular

communication in monocultures and co-cultures of primary

microvascular endothelial cells and buccal fibroblasts based

on the collagen matrix Bio-Gide®. To achieve this objective we

analyzed the secretion patterns of relevant angiogenic factors

such as VEGF, Ang 1, Ang 2, bFGF and eNOS and evaluated their

effect on cellular parameters such as viability, proliferation,

migration and tube formation. The results showed complex

interactions of the investigated growth factors. A distinct

influence of the co-cultivation, the spatial separation and

the used collagen matrices on the expression patterns of the

primary cells could be demonstrated. The co-cultivation of

endothelial cells and fibroblasts led to increased levels of

VEGF, bFGF, eNOS and Ang-2 compared to the monocultures.

Interestingly, a spatial separation of the two cell types as well

as the cultivation on the used collagen matrices enhanced this

effect additionally. The gained results help us to understand

the cellular interaction in complex multi-cultures and may lead

to optimized cultivation approaches for tissue engineering of

complex tissues.

Speaker Biography

Martin Heller has completed his PhD in Biology at the Max Planck Institute of Polymer

Research Mainz in 2013. Afterwards he worked as Postdoc at the University Medical

Center of Mainz and started to study Medicine in April 2014. His focus of research is the

modification of biomaterials in the context of artificially generated tissue equivalents in

complex multi-cultures of primary human cells

e:

martin.heller@uni-mainz.de

Martin Heller

, Robotics & Biomaterials 2018, Volume 29

DOI: 10.4066/biomedicalresearch-C6-016