2005
DOI: 10.1016/j.jneumeth.2004.08.011
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Photo-chemically patterned polymer surfaces for controlled PC-12 adhesion and neurite guidance

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Cited by 61 publications
(52 citation statements)
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“…High-energy light, such as deep UV light below 200nm (Azioune et al, 2010) or concentrated light from pulsed lasers (see panel C) (Doyle et al, 2009), have also proved useful to create local plasma and directly oxidise culture substrates without the need for dedicated photo-chemistry. Exposure to plasma renders hydrophobic polystyrene culture substrates hydrophilic (Welle and Gottwald, 2002;Welle et al, 2005) and also destroys the protein and cell repellent properties of PEG (Azioune et al, 2009), thus allowing for further protein grafting.Most of these methods can be repeated to micropattern several distinct proteins at specific locations (multi-patterning), as long as each step preserves the preceding protein coating. Repeated micro-contact printing steps are difficult to perform, as they require to align all printing steps.…”
mentioning
confidence: 99%
“…High-energy light, such as deep UV light below 200nm (Azioune et al, 2010) or concentrated light from pulsed lasers (see panel C) (Doyle et al, 2009), have also proved useful to create local plasma and directly oxidise culture substrates without the need for dedicated photo-chemistry. Exposure to plasma renders hydrophobic polystyrene culture substrates hydrophilic (Welle and Gottwald, 2002;Welle et al, 2005) and also destroys the protein and cell repellent properties of PEG (Azioune et al, 2009), thus allowing for further protein grafting.Most of these methods can be repeated to micropattern several distinct proteins at specific locations (multi-patterning), as long as each step preserves the preceding protein coating. Repeated micro-contact printing steps are difficult to perform, as they require to align all printing steps.…”
mentioning
confidence: 99%
“…It is well established that the microenvironment of a cell greatly influences its state of differentiation, and one of the great challenges of tissue engineering has been the precise control of cell-cell contacts. 185 One classic example is the primary hepatocyte, which rapidly loses a number of hepatocytespecific markers, such as cytochrome P-450 186 , albumin, and urea 187 once removed from its natural environment. This loss of function can be ameliorated by coculture with nonparenchymal cells.…”
Section: Cell Patterning and Directed Growthmentioning
confidence: 99%
“…Functional studies have therefore been hindered by these ill-defined arrangements that do not accurately capture in vivo geometries and connectivities (49). To address this need, researchers have adapted microtechnologies for engineering substrates with defined biochemical patterns and topographical features.…”
Section: Microtechnologiesmentioning
confidence: 99%
“…Micropatterned Cues. Many methods exist for patterning substrates with biochemical cues (49). Microcontact printing is a common technique used to pattern substrates with a silicone rubber stamp ''inked'' with peptides, proteins, or other cell adhesion-promoting factors.…”
Section: Microtechnologiesmentioning
confidence: 99%
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