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Graphene for improved femtosecond laser based pluripotent stem cell transfection

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dc.contributor.author Mthunzi-Kufa, Patience
dc.contributor.author He, K
dc.contributor.author Ngcobo, Sandile
dc.contributor.author Khanyile, T
dc.contributor.author Warner, JH
dc.date.accessioned 2014-08-19T06:39:20Z
dc.date.available 2014-08-19T06:39:20Z
dc.date.issued 2014-05
dc.identifier.citation Mthunzi, P, He, K, Ngcobo, S, Khanyile, T and Warner, J.H. 2014. Graphene for improved femtosecond laser based pluripotent stem cell transfection. Journal of Biophotonics, vol. 7(5), pp 351-352 en_US
dc.identifier.issn 1864-063X
dc.identifier.uri http://onlinelibrary.wiley.com/doi/10.1002/jbio.201300028/abstract;jsessionid=C56FCE53FAC5A63970867CAC3556AE68.f01t01
dc.identifier.uri http://hdl.handle.net/10204/7612
dc.description Copyright: 2014 Wiley. This is an ABSTRACT ONLY. The definitive version is published in Journal of Biophotonics, vol. 7(5), pp 351-352 en_US
dc.description.abstract Pluripotent stem cells are hugely attractive in the tissue engineering research field as they can self-renew and be selectively differentiated into various cell types. For stem cell and tissue engineering research it is important to develop new, biocompatible scaffold materials and graphene has emerged as a promising material in this area as it does not compromise cell proliferation and accelerates specific cell differentiation. Previous studies have shown a non-invasive optical technique for mouse embryonic stem (mES) cell differentiation and transfection using femtosecond (fs) laser pulses. To investigate cellular responses to the influence of graphene and laser irradiation, here we present for the first time a study of mES cell fs laser transfection on graphene coated substrates. First we studied the impact of graphene on Chinese Hamster Ovary (CHO-K1) cell viability and cell cytotoxicity in the absence of laser exposure. These were tested via evaluating the mitochondrial activity through adenosine triphosphates (ATP) luminescence and breakages on the cell plasma membrane assessed using cytosolic lactate dehydrogenase (LDH) screening. Secondly, the effects of fs laser irradiation on cell viability and cytotoxicity at 1064 and 532 nm for cells plated and grown on graphene and pure glass were assessed. Finally, optical transfection of CHO-K1 and mES cells was performed on graphene coated versus plain glass substrates. Our results show graphene stimulated cell viability whilst triggering a mild release of intracellular LDH. We also observed that compared to pure glass substrates; laser irradiation at 1064 nm on graphene plates was less cytotoxic. Finally, in mES cells efficient optical transfection at 1064 (82%) and 532 (25%) nm was obtained due to the presence of a graphene support as compared to pristine glass. Here we hypothesize an up-regulation of cell adhesion promoting peptides or laminin-related receptors of the extracellular matrix (ECM) in cell samples grown and irradiated on graphene substrates. By bringing together advances in optics and nanomaterial sciences we demonstrate pathways for enhancement of pluripotent stem cell biology. en_US
dc.language.iso en en_US
dc.publisher Wiley-VCH Verlag en_US
dc.relation.ispartofseries Workflow;13196
dc.subject Graphene en_US
dc.subject Cell viability and cytotoxicity en_US
dc.subject Femtosecond laser transfection en_US
dc.subject Pluripotent stem cells en_US
dc.title Graphene for improved femtosecond laser based pluripotent stem cell transfection en_US
dc.type Conference Presentation en_US
dc.identifier.apacitation Mthunzi, P., He, K., Ngcobo, S., Khanyile, T., & Warner, J. (2014). Graphene for improved femtosecond laser based pluripotent stem cell transfection. Wiley-VCH Verlag. http://hdl.handle.net/10204/7612 en_ZA
dc.identifier.chicagocitation Mthunzi, P, K He, Sandile Ngcobo, T Khanyile, and JH Warner. "Graphene for improved femtosecond laser based pluripotent stem cell transfection." (2014): http://hdl.handle.net/10204/7612 en_ZA
dc.identifier.vancouvercitation Mthunzi P, He K, Ngcobo S, Khanyile T, Warner J, Graphene for improved femtosecond laser based pluripotent stem cell transfection; Wiley-VCH Verlag; 2014. http://hdl.handle.net/10204/7612 . en_ZA
dc.identifier.ris TY - Conference Presentation AU - Mthunzi, P AU - He, K AU - Ngcobo, Sandile AU - Khanyile, T AU - Warner, JH AB - Pluripotent stem cells are hugely attractive in the tissue engineering research field as they can self-renew and be selectively differentiated into various cell types. For stem cell and tissue engineering research it is important to develop new, biocompatible scaffold materials and graphene has emerged as a promising material in this area as it does not compromise cell proliferation and accelerates specific cell differentiation. Previous studies have shown a non-invasive optical technique for mouse embryonic stem (mES) cell differentiation and transfection using femtosecond (fs) laser pulses. To investigate cellular responses to the influence of graphene and laser irradiation, here we present for the first time a study of mES cell fs laser transfection on graphene coated substrates. First we studied the impact of graphene on Chinese Hamster Ovary (CHO-K1) cell viability and cell cytotoxicity in the absence of laser exposure. These were tested via evaluating the mitochondrial activity through adenosine triphosphates (ATP) luminescence and breakages on the cell plasma membrane assessed using cytosolic lactate dehydrogenase (LDH) screening. Secondly, the effects of fs laser irradiation on cell viability and cytotoxicity at 1064 and 532 nm for cells plated and grown on graphene and pure glass were assessed. Finally, optical transfection of CHO-K1 and mES cells was performed on graphene coated versus plain glass substrates. Our results show graphene stimulated cell viability whilst triggering a mild release of intracellular LDH. We also observed that compared to pure glass substrates; laser irradiation at 1064 nm on graphene plates was less cytotoxic. Finally, in mES cells efficient optical transfection at 1064 (82%) and 532 (25%) nm was obtained due to the presence of a graphene support as compared to pristine glass. Here we hypothesize an up-regulation of cell adhesion promoting peptides or laminin-related receptors of the extracellular matrix (ECM) in cell samples grown and irradiated on graphene substrates. By bringing together advances in optics and nanomaterial sciences we demonstrate pathways for enhancement of pluripotent stem cell biology. DA - 2014-05 DB - ResearchSpace DP - CSIR KW - Graphene KW - Cell viability and cytotoxicity KW - Femtosecond laser transfection KW - Pluripotent stem cells LK - https://researchspace.csir.co.za PY - 2014 SM - 1864-063X T1 - Graphene for improved femtosecond laser based pluripotent stem cell transfection TI - Graphene for improved femtosecond laser based pluripotent stem cell transfection UR - http://hdl.handle.net/10204/7612 ER - en_ZA


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