Abstract
Introduction:
The integration of engineered tissues after implantation is limited due to the lack of a vascular network. When vascular networks are included, they generally are not organized, or lose their initial organization fast1. Due to the ability of cells to sense their environment by mechanotransduction, signaling, maturation, organization and cell survival is regulated. The objective of this study is to analyze the combinatory effect of substrate stiffness and fluid flow on vascular organization and maturation to find the basic parameters for pre-vascularization of engineered tissue.
Methods
A microfluidic PDMS framed system was used, which makes it possible to investigate different hydrogel compositions in parallel. Pre-glycation by D-(-)-Ribose allowed for the use of one type of hydrogel in the same concentration but with different modulated mechanical properties. During the polymerization process of the hydrogels, needles were integrated into the gels to create hollow channels by their removing afterwards. The down and top side of the system were sealed with thin cover glasses to ensure the visibility of the inner system. The fluid-flow channels were coated with 0.1% Gelatin to improve the cell attachment and seeded with Smooth muscle cells. Afterwards Human Umbilical Vein Endothelial Cells (HUVECs) were seeded on top of the smooth muscle cells to mimic the physiological blood vessel structure. An additional channel was filled with VEGF (50 ng/mL), which is known as one of the main angiogenic factors which diffuse into the hydrogel over time2. Different fluid-flow profiles were applied to the cell seeded channels. The newly formed capillary network was analyzed by ImageJ.
Results:
The pre-glycation by incubation of different concentrations of D-(-)-Ribose resulted in an increase of stiffness of the same type of hydrogel by additionally crosslinking of the different hydrogels components. The use of different modulated hydrogels allowed for the simultaneous analysis of the effect of fluid flow on the vascular sprouting into the hydrogels triggered by the diffused VEGF. Different mechanical properties in combination with different fluid flow patterns affected the ability of HUVEC to migrate and organize into the hydrogels and show differences in the sprouting morphology.
Outlook:
To mimic the physiological state, different Endothelial cell types (e.g. HUVECs, HMECs, HIAEC) will be integrated into the fluid flow channels. This will allow us to see if different endothelial cell origins leads to a different sprouting behavior or if the already described endothelial plasticity leads to similar results.
The integration of engineered tissues after implantation is limited due to the lack of a vascular network. When vascular networks are included, they generally are not organized, or lose their initial organization fast1. Due to the ability of cells to sense their environment by mechanotransduction, signaling, maturation, organization and cell survival is regulated. The objective of this study is to analyze the combinatory effect of substrate stiffness and fluid flow on vascular organization and maturation to find the basic parameters for pre-vascularization of engineered tissue.
Methods
A microfluidic PDMS framed system was used, which makes it possible to investigate different hydrogel compositions in parallel. Pre-glycation by D-(-)-Ribose allowed for the use of one type of hydrogel in the same concentration but with different modulated mechanical properties. During the polymerization process of the hydrogels, needles were integrated into the gels to create hollow channels by their removing afterwards. The down and top side of the system were sealed with thin cover glasses to ensure the visibility of the inner system. The fluid-flow channels were coated with 0.1% Gelatin to improve the cell attachment and seeded with Smooth muscle cells. Afterwards Human Umbilical Vein Endothelial Cells (HUVECs) were seeded on top of the smooth muscle cells to mimic the physiological blood vessel structure. An additional channel was filled with VEGF (50 ng/mL), which is known as one of the main angiogenic factors which diffuse into the hydrogel over time2. Different fluid-flow profiles were applied to the cell seeded channels. The newly formed capillary network was analyzed by ImageJ.
Results:
The pre-glycation by incubation of different concentrations of D-(-)-Ribose resulted in an increase of stiffness of the same type of hydrogel by additionally crosslinking of the different hydrogels components. The use of different modulated hydrogels allowed for the simultaneous analysis of the effect of fluid flow on the vascular sprouting into the hydrogels triggered by the diffused VEGF. Different mechanical properties in combination with different fluid flow patterns affected the ability of HUVEC to migrate and organize into the hydrogels and show differences in the sprouting morphology.
Outlook:
To mimic the physiological state, different Endothelial cell types (e.g. HUVECs, HMECs, HIAEC) will be integrated into the fluid flow channels. This will allow us to see if different endothelial cell origins leads to a different sprouting behavior or if the already described endothelial plasticity leads to similar results.
| Original language | English |
|---|---|
| Publication status | Published - 8 Jul 2018 |
| Event | 8th World Congress of Biomechanics, WCB 2018 - Convention Centre Dublin, Dublin, Ireland Duration: 8 Jul 2018 → 12 Jul 2018 Conference number: 8 http://wcb2018.com/ |
Conference
| Conference | 8th World Congress of Biomechanics, WCB 2018 |
|---|---|
| Abbreviated title | WCB |
| Country/Territory | Ireland |
| City | Dublin |
| Period | 8/07/18 → 12/07/18 |
| Internet address |
Keywords
- Microfluidic channel
- Vascular tissue engineering
- microfluidic chip
- Modelling and simulation
- Endothelial cell
- Diffusion
- Fluid flow modeling