Silicon substrate as a novel cell culture device for myoblast cells
© Bhuyan et al.; licensee BioMed Central Ltd. 2014
Received: 21 February 2014
Accepted: 5 May 2014
Published: 16 May 2014
Tissue and organ regeneration via transplantation of cell bodies in-situ has become an interesting strategy in regenerative medicine. Developments of cell carriers to systematically deliver cell bodies in the damage site have fall shorten on effectively meet this purpose due to inappropriate release control. Thus, there is still need of novel substrate to achieve targeted cell delivery with appropriate vehicles. In the present study, silicon based photovoltaic (PV) devices are used as a cell culturing substrate for the expansion of myoblast mouse cell (C2C12 cells) that offers an atmosphere for regular cell growth in vitro. The adherence, viability and proliferation of the cells on the silicon surface were examined by direct cell counting and fluorescence microscopy.
It was found that on the silicon surface, cells proliferated over 7 days showing normal morphology, and expressed their biological activities. Cell culture on silicon substrate reveals their attachment and proliferation over the surface of the PV device. After first day of culture, cell viability was 88% and cell survival remained above 86% as compared to the seeding day after the seventh day. Furthermore, the DAPI staining revealed that the initially scattered cells were able to eventually build a cellular monolayer on top of the silicon substrate.
This study explored the biological applications of silicon based PV devices, demonstrating its biocompatibility properties and found useful for culture of cells on porous 2-D surface. The incorporation of silicon substrate has been efficaciously revealed as a potential cell carrier or vehicle in cell growth technology, allowing for their use in cell based gene therapy, tissue engineering, and therapeutic angiogenesis.
KeywordsCell culturing Photovoltaic effect Silicon substrate Cell carrier
Cell based therapies are very promising for therapeutic treatment of various diseases and disorders. Cell therapies offer key advantages that include rapid isolation from the host body, and in vitro extensive proliferation. Bio processed cells in the various forms provide unique potential to customize the cells to damage sites where the cells or tissues are required as therapeutic agent. Laboratory processed cells can be delivered to targeted site of patient [1–3]; however, cell delivery via cell substrate provides mechanical and biological support for attachment and proliferation [4, 5] of cells. Compare to three dimensional (3D) cell structures, thin two dimensional (2D) cell construct does not required complicated microvasculature and are easy to fabricate and handle . In our investigation silicon based photovoltaic (PV) devices are used as cell culturing substrates for mammalian myoblast cells, C2C12.
Due to proper integration of electronics and biological systems, Silicon is widely used in biomedical application such as functional electrode stimulation , Parkinson’s disease , Electrode-neuron implants , and devices for drug delivery . Silicon substrate fabricated in micro electromechanical systems (MEMS) reveal biocompatibility without adverse affect or reaction with living tissues or organ . Experimental investigation shows that during implantation of biomedical equipment, sufficient cell attachment to the silicon surface is key issue . To enhance cell adhesion on the silicon surface Maher et al. , and Martinoia  used bioactive molecules coating such as polylysine, and laminin respectively. Certainly incorporation of biomolecule coatings retained more cells on the silicon based implants; however, without accumulating biomolecules, a more porous and microstructured silicon substrate will be better for direct cell adhesion.
In this paper, we describe the use of a commercially available monocrystaline silicon PV device to be used as substrate for culturing of C2C12 mammalian cells. C2C12 is a muscle-like cell line that can form myuotubes for differentiation of myoblasts. This investigation suggests that porous microstructure based silicon is very promising biomaterials, potentially can be used as cell carrier or vehicle for the delivery of therapeutics. To illustrate the presentation of this innovative strategy, we assessed the attachment and growth of C2C12 cells in porous biocompatible silicon surfaces. The assessment of cell attachment, viability and the morphological properties of adherent cells were accomplished using direct cell counting machine, Lived/Dead assay, and 4′, 6-diamidino-2-phenylindole dihydrochloride (DAPI) fluorescence immunostaining.
Silicon substrate preparation
Silicon based photovoltaic (PV) devices that convert the energy of sunlight directly into electricity by the photovoltaic effect were used as silicon substrate for cell culturing. Commercially available, 0.8 inch × 1.66 inch (2 cm × 4 cm), PV cells were obtained from electronic retail store RadioShack® (Custom assembled in USA). PV devices were prepared to avoid medium leakage as described in  putting a nontoxic biocompatible glues walled. Glue walled PV cells were Ultra Violet (UV)/Ozone cleaned for 2.5 minutes to remove surface contamination . Subsequently they were soaked in 70% methanol over night and air dried in a sterile ventilated hood. Upon drying, cells were covered with aluminum foil and kept in the dark to remove electrical charge from the PV devices.
Anchorage dependent myoblasts C2C12 mammalian were collected from American Type Culture Collection, ATCC (CRL-1772) grown in Dulbecco’s Modified Eagle’s Medium (DMEM) enhanced with 1% antibiotics, 2 mM glutamine, 10% fetal bovine serum, at pH 7.5. Confluent cultured of C2C12cells washed with PBS, detached from petri dish by trypsinizing (.25% trypsin, Sigma Co., St. Louis, MO). Trypsinated cell-medium solution was centrifuged to get cell pallet to seed cell on the PV devices @ 12,000/cm2. The cell cultures were maintained in DMEM growth medium and incubated maintaining 5% CO2 atmosphere at 37°C, and 100% humidity. Every 24 hours cells were washed and changed medium as required. Anchorage dependent C2C12 cells were capable of differentiating after attachment to the silicon surface and cell were cultured for seven days. For cell counting and determine the viability cells were isolated from the PV devices using trypsin and scrapper.
Cell Fixation and Staining
C2C12 monolayers attached to PV surfaces were washed two times or more with phosphate-buffered saline (PBS), maintaining the level at pH 7.4, and fixed with 3.7% formaldehyde following incubation for 5-10 minutes. After removing formaldehyde, cells were rinsed three times with PBS to stop fixation. After rinsing, the nuclei of the cells were labeled with 0.1μg/ml DAPI (Sigma-Aldrich, Sweden, 300 nM) and incubated for 15-20 minutes. Subsequently, PV surfaces were cleaned, perfectly washing with PBS twice. The samples were then mounted and observed under an inverted fluorescence microscope (Zeiss Eclipse E800).
Result and discussion
Cell Quantification and Viability
Microscopy and Live/Dead Staining
Myoblast cells were observed under inverted light microscope (Olympus IX71). The viability of cell line was investigated using a two-color fluorescence live/dead assay (LIVE/DEAD® reduced biohazard Viability/Cytotoxicity Kit #1) and using a solution consisting of SYTO 10 green fluorescent nucleic acid stain dissolved in DMSO and DEAD read nucleic acid stain dissolved in DMSO (Invitrogen, Stockholm, Sweden). The samples were viewed using a fluorescent confocal microscope Nikon ECLIPSE Ti, and the viability of the cells were evaluated by observing the number of cells stained with SYTO 10 (green). Trypsinized cells from the PV devices were centrifuged and supernatant was replaced by diluted dye mixture (Component A, Component B, and a FBS as 2:2:1000); 200–500 μL were placed on top to cover the cell pallet. After 15 minutes incubation of the dye-cell mixture, solution was replaced with fresh PBS. 4% glutaraldehyde was added in PBS, and incubated for at least 15 minutes and put required amount of cell suspension in on glass cover slip before observation.
Cell Proliferation by DNA Quantification
To stimulate the regeneration of tissues by cell delivery methods, it is a prime requirement that the suggested biomaterials serving as cell substrates or cell carrier must maintain its structure and functionality under physiological conditions to mimic in vivo condition . In our in vitro pilot study we observed that mammalian cells attached and proliferated such a manner that resembles their native cell curve profile: lag, log, stationary, and death phases chronologically shown in Figure 1. Culturing of myoblast muscle cells in vitro on silicon PV devices micro or nano scale surface topography characterizes a feasible technique for interfacing cells and Silicon-based implants even electronics devices. In our experimental studies we utilize silicon substrate that is used as PV cells for power generation by simple manufacturing process without complicated procedure or surface modification. The silicon substrates can be easily used as transporters in cell delivery systems. Finally, the cell growth profile revealed that monocrystalline poroused silicon can be offered as potential cellular vehicle to support the viability and proliferation even long-term cell culturing for potential organ/tissue repair and/or cell mediated gene delivery.
Traditionally PV cell have been used as a clean renewable source of energy. Our study has developed a breakthrough technology in the cell culturing and cell growth using of PV device. This study explored the biological applications of silicon based PV devices, demonstrating its biocompatibility properties and found useful for culture of cells on porous 2-D surface. In future, cells loaded on top of biodegradable silicon devices can be implanted to the host body with cell implant and after biodegradation cell can be migrated to repair damage tissue or organ. Even micro-sized silicon cells loaded with biological cells can be introduced to the damage area with catheter or intravenous injection. In our pilot study we demonstrate the feasibility of anchorage dependent cells culture on micro porous silicon substrate. Further formulation optimization studies are needed to improve the efficiency of cell attachment and viability. Extensive research and development of attaching and releasing more drugs from PV cell also need to be developed both in vitro and in vivo.
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