Data · collection · 2019
Supplementary Information for: Conducting polymer-based multilayer films for instructive biomaterial coatings
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Description
Abstract
Cells inhabit environments known as the extracellular matrix (ECM) which consists of a mixture of different biomolecules, and the precise composition and topographical properties are different in different tissues (e.g., bone, brain, muscle, skin). Cells interact intimately with the ECM, not only constructing the biomolecules, but assist its organization in 3D space, and its degradation (which is important for tissue remodeling); reciprocally, cells respond to the ECM (e.g., by modifying their size, shape, etc).
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Cellular alignment is observed in organs and tissues such as bones, muscles and skin, and this alignment is important for the healthy functioning of the organ/tissue. Here, we present a novel method of aligning cells on biomaterials, simply by applying an electrical current through the biomaterial. Supplementary Figure S1 - Experimental setup for dip coating multilayer films using a Gilson 223 Sample Changer converted for use as a dip coater.
Supplementary Figure S2 - Scatter plot correlating the relationship between the cell orientation (angle relative to the dipping direction of the multilayer films) and length of the cells on the polymer films without and with electrical stimulation. A) PEDOT-PSS-based films. B) PEDOT-S-based films.
Black circles represent cells without electrical stimulation, whereas red circles represent cells with electrical stimulation; black and red lines represent the corresponding trend lines. Supplementary Figure S3 HUMAN MESENCHYMAL STEM CELL ADHESION STUDIES HMSCs were supplied by Lonza (Walkersville, MD). Samples were prepared as described above.
After sterilization, the samples were incubated for 30 minutes in 24 well plates containing HMSC growth medium that was composed of: high glucose Dulbecco’s Modified Eagle Medium (DMEM, 440 mL); fetal bovine serum (50 mL); antibiotic-antimycotic (5 mL); non-essential amino acids (5 mL), and 2 ng mL-1 basic fibroblast growth factor. Medium was aspirated and replaced prior to HMSC seeding. Cell viability before starting the experiment was determined by the Trypan Blue exclusion method, and the measured viability exceeded 95 % in all cases.
HMSCs were seeded at 5,000 cells cm-2, and incubated at 37 °C, 95 % humidity, and a CO2 content of 5 %. Samples were fixed and stained as decribed above (n = 3). - HMSCs on multilayer films after 3 days in culture. A) PEDOT-PSS-based multilayer films.
B) PEDOT-S-based multilayer films. DAPI-stained nuclei are blue and Alexa Fluor® 488-stained actin is green. Scale bars represent 150 µm.
Supplementary ZIP file – LabVIEW script and associated files for control of Gilson 223 Sample Changer as a dip coater
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- DOI doi.org/10.25402/fsoa.c.4443026 ↗
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Topics
- Stated by source
- Basic medicine · Biological sciences
- Inferred from text
- Cellular interactions 80%
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