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dc.contributor.authorDhawan, Udeshen_US
dc.contributor.authorLee, Chia Huien_US
dc.contributor.authorHuang, Chun-Chungen_US
dc.contributor.authorChu, Ying Haoen_US
dc.contributor.authorHuang, Guewha S.en_US
dc.contributor.authorLin, Yan-Renen_US
dc.contributor.authorChen, Wen-Liangen_US
dc.date.accessioned2019-04-03T06:36:18Z-
dc.date.available2019-04-03T06:36:18Z-
dc.date.issued2015-11-09en_US
dc.identifier.issn1477-3155en_US
dc.identifier.urihttp://dx.doi.org/10.1186/s12951-015-0144-yen_US
dc.identifier.urihttp://hdl.handle.net/11536/128373-
dc.description.abstractBackground: Nitric oxide (NO) plays a very important role in the cardiovascular system as a major secondary messenger in signaling pathway. Its concentration regulates most of the important physiological indexes including the systemic blood pressure, blood flow, regional vascular tone and other cardiac functions. The effect of nanotopography on the NO secretion in cardiomyocytes has not been elucidated before. In this study, we report how the nanotopography can modulate the secretion profile of NO and attempt to elucidate the genetic pathways responsible for the same by using Tantalum Oxide nanodot arrays ranging from 10 to 200 nm. A series of nanodot arrays were fabricated with dot diameter ranging from 10 to 200 nm. Temporal NO release of cardiomyocytes was quantified when grown on different surfaces. Quantitative RT-PCR and Western blot were performed to verify the genetic pathways of NO release. Results: After hours 24 of cell seeding, NO release was slowly enhanced by the increase of dot diameter from 10 nm up to 50 nm, mildly enhanced to a medium level at 100 nm, and increase rapidly to a high level at 200 nm. The temporal enhancement of NO release dropped dramatically on day 3. On day 5, a topology-dependent profile was established that maximized at 50 nm and dropped to control level at 200 nm. The NO releasing profile was closely associated with the expression patterns of genes associated with Endothelial nitric oxide synthase (eNOS) pathway [GPCR, PI3K, Akt, Bad, Bcl-2, NF kappa B(p65), eNOS], but less associated with Inducible nitric oxide synthase (iNOS) pathway (TNF-alpha, ILK, Akt, I kappa Ba, NF kappa B, iNOS). Western blotting of Akt, eNOS, iNOS, and NF kappa B further validated that eNOS pathway was modulated by nanotopology. Conclusions: Based on the findings of the present study, 50, 100 nm can serve as the suitable nanotopography patterns for cardiac implant surface design. These two nanodot arrays promote NO secretion and can also promote the vascular smooth muscle relaxation. The results of this study can improve the heart stent design in the medical treatments.en_US
dc.language.isoen_USen_US
dc.subjectTantalum oxideen_US
dc.subjectNanodotsen_US
dc.subjectCardiomyocytesen_US
dc.subjecteNOSen_US
dc.subjectiNOSen_US
dc.subjectSignaling pathwayen_US
dc.titleTopological control of nitric oxide secretion by tantalum oxide nanodot arraysen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/s12951-015-0144-yen_US
dc.identifier.journalJOURNAL OF NANOBIOTECHNOLOGYen_US
dc.citation.volume13en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000364299600001en_US
dc.citation.woscount4en_US
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