2003
DOI: 10.1016/s0021-9797(02)00163-7
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The effect of surface wettability on induction and growth of neurites from the PC-12 cell on a polymer surface

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Cited by 141 publications
(116 citation statements)
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“…Both discrete specimens and surface energy gradients were used in these studies and many different outcomes have been observed. In some studies, cell functions are enhanced on hydrophilic surfaces, 119,[125][126][127] whereas in others, cell functions are enhanced on hydrophobic surfaces. [128][129][130][131] While in other cases, surface energy has no effect on cell functions 131,132 or cell functions have a maximum at an intermediate surface energy.…”
mentioning
confidence: 99%
“…Both discrete specimens and surface energy gradients were used in these studies and many different outcomes have been observed. In some studies, cell functions are enhanced on hydrophilic surfaces, 119,[125][126][127] whereas in others, cell functions are enhanced on hydrophobic surfaces. [128][129][130][131] While in other cases, surface energy has no effect on cell functions 131,132 or cell functions have a maximum at an intermediate surface energy.…”
mentioning
confidence: 99%
“…It is noteworthy that the physicochemical characteristics of the membranes in terms of hydrophobicity/hydrophilicity (wettability) could guide neuronal cell responses by strongly influencing cell adhesion and growth. It has been reported that neuronal cells preferentially adhere to surfaces with moderate hydrophilicity [Lee et al, 2003]. Indeed, in the case of superhydrophilic surfaces, the proteins that mediate cell adhesion are not well bound on the surface and do not ensure a strong and valuable cell attachment.…”
Section: Discussionmentioning
confidence: 99%
“…PC-12 cells (KCLB 21721, Korea Cell Line Bank, Korea) were cultured in Dulbecco's modified Eagles medium (DMEM, GIBCO BRL Co., USA) with L-glutamine, supplemented with 15% in activated donor calf serum (CS, GIBCO BRL) and antibiotic/antimycotic (penicillin 10,000 U/mL, streptomycin 10,000 cgm/mL, and amphotericin B 25 μg/mL, GIBCO BRL) in tissue culture polystyrene flask (Falcon, Co., USA) at 37 ο C under 5% CO 2 atmosphere. 9,10,36 To observe NGF bioactivity after release of NGF at scheduled time, PC-12 cells were plated at a density of 8 Ý 10 4 cells/cm 2 onto the NGF-loaded PLGA films eliminated with NGF released aqueous solution in 12-well plate for 7 days. After incubation at 37 ο C under 5% CO 2 atmosphere, the PLGA surfaces were washed with PBS and the PC-12 cells attached on the surfaces were fixed with 2.5% glutaraldehyde (GIBCO BLR) in PBS for 24 hrs at room temperature.…”
Section: Methodsmentioning
confidence: 99%
“…In our previous study, 9,10,36 we studied NGF-loaded PLGA devices such as microspheres and scaffolds for the possibility of the application of neural tissue engineering. One of the significant disadvantages is the massive initial burst from the surface of NGF loaded microspheres and interconnected pores of the PLGA scaffolds and the massive loss during the preparation process resulting in no detection of accurate NGF concentration.…”
Section: Introductionmentioning
confidence: 99%