Team:LMU-TUM Munich/Hypoxia
Fighting hypoxia in printed tissue
Unicellular organisms such as bacteria posses the ability to reproduce very quickly, when given the right conditions such as warmth, moisture and suitable nutrients [1] and enter an inactive state when these are limited. On the contrary, most multicellular systems depend on a steady, adequate supply of oxygen and nutrients essential for their survival and metabolic stability.
Herein lies one of the main challenges of bioprinting approaches.
When printing, the homogenous delivery of oxygen to three-dimensional cell-constructs is limited by diffusion gradients in tissue from the periphery towards the center [2]- ↑ http://www.bbc.co.uk/schools/gcsebitesize/science/triple_ocr_gateway/beyond_the_microscope/understanding_microbes/revision/2/
- ↑ AMA-Volkmer, Elias, et al. "Hypoxia in static and dynamic 3D culture systems for tissue engineering of bone." Tissue Engineering Part A 14.8 (2008): 1331-1340.<\ref>, thus resulting in tissue hypoxia(3).
In our bodies, this need for oxygen supply is met by blood vessels, which form extensive networks that nurture all tissues. As a result, capillaries grow and regress in healthy tissues according to functional demands. Thereby, no metabolically active tissue in the body is more than a few hundred micrometers from a blood capillary, which is formed by the process of angiogenesis. (4)
Sprouting angiogenesis, as implied by its name is characterized by sprouts composed of endothelial cells, which usually grow toward an angiogenic stimulus.
This driving stimulus is initiated in poorly perfused tissues when oxygen sensing mechanisms detect a level of hypoxia that demands the formation of new blood vessels to satisfy the metabolic requirements of parenchymal cells. Most types of parenchymal cells respond to a hypoxic environment by secreting a key proangiogenic growth factor called vascular endothelial growth factor (VEGF-A). (4)
Because the production of a normal vasculature is among others heavily dependent upon the concentration of VEGF-A in the tissue, we have constructed a model in order to measure the hypoxia dependent secretion of VEGF and PDGF, thus simulating the extreme conditions that might be present when printing several layers of tissue and that, by triggering sprouting angiogenesis would eo ipso add blood vessels to portions of tissues previously devoid of them.
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Hypoxia-inducible promoters
Hypoxia refers to subnormal levels of oxygen in air, blood and tissue. Tissue hypoxia leads to cellular dysfunction and ultimately can lead to cell death, and the ability of cells to adapt to periods of hypoxia is therefore important for their survival.(5)
In this context, we wanted to find a most suitable way to compensate the poor oxygen conditions generated when layer-printing.
Following the idea to enhance the level of hypoxic induction and to control target gene expression(7), we have designed a potent hypoxia-inducible promoter inspired by the approach made by Lee, J. Y., et al. "A novel chimeric promoter that is highly responsive to hypoxia and metals."
Many hypoxia-responsive genes are regulated by the hypoxia-response element (HRE) protein family of transcription factors, including hypoxia-inducible factor-1 (HIF-1).(7) When HREs derived from different genes are placed in plasmids, they confer hypoxia inducibility upon heterologous promoters in various cell types.2
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Constructs and methodology
In order to test hypoxia-dependent gene expression, we created luciferase constructs that allow the quantification of expression levels via a luciferase assay. The expression of these constructs is driven by a hypoxia-inducible promoter, which results in the translation of a luciferase and its secretion into the medium. By taking samples of the medium after 12 h and 24 h after the exposure of HEK293T cells to hypoxia (8% CO2, 92% N2) and measuring luciferase activity by a corresponding assay, we are able to quantify hypoxia-dependent gene expression. In order to determine whether gene expression is really only responsive to hypoxia - but inactive during normal oxygen concentrations - a control at normal oxygen concentrations (21%) was furthermore run.
For the assay, a total of eight constructs were tested, six of which are luciferase constructs for the quantification of expression levels and two of which are VEGF-constructs that are used to confirm the expression of the actual growth factor by our cells. Luciferase constructs all contain the hypoxia promoter, a signal peptide, a coding sequence and a polyadenylation signal, but vary in the number of hypoxia-response elements.
Of the two constructs that do not contain a luciferase, but the actual growth factors (VEGF and PDGF), one is expressed via a hypoxia-promoter (4x HRE) and one via a CMV promoter as a positive control. Expression levels are hereby determined via an ELISA.
Results
Discussion
Two interesting observations were made as a result of the luciferase assays and the ELISA.
- Although two of the nanoluciferase constructs did not seem to be functional (hypoxia promoter with 2x HRE and 4x HRE), a tendency could be observed for the others - showing that the number of HREs positively correlates with expression levels - the construct with 8x HREs showing the highest absolute secretion of luciferases.
- Expression levels compared between hypoxia and normoxia do not significantly differ, making the promoter created by us not actually responsive towards states of low oxygen. High. Still, in comparison to the CMV promoter, the hypoxia promoter does not lose activity upon exposing cells to hypoxia, but remains remarkably steady. The HRE elements may hereby actually counter-act the effects of reduced transcription due to hypoxia-mediated stress signalling.
References
