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Cardiac ECM Structure-Mimetic Electrospun Scaffolds Reinstate Healthy Cardiomyocyte Phenotype

dc.creatorRath, Rutwik
dc.date.accessioned2020-08-22T20:35:15Z
dc.date.available2014-07-26
dc.date.issued2014-07-26
dc.identifier.urihttps://etd.library.vanderbilt.edu/etd-07252014-110513
dc.identifier.urihttp://hdl.handle.net/1803/13586
dc.description.abstractAlthough extracellular matrix (ECM) composition and organization are considered important regulators of cardiomyocyte phenotype in vitro and in vivo, a causal relationship between the ECM structure and effect on maintenance of cardiomyocyte (CM) phenotype has not been established. In this study, we investigated how key structural characteristics of electrospun scaffolds (fiber alignment, spacing, and diameter) regulated CM phenotype – specifically cell morphology, actin/myosin patterning, and cardiac gene expression. We found that aligned fiber scaffolds resulted in a longer, more rod shaped morphology in both neonatal and adult CMs. Along with better morphology, CMs were also found to have better-organized cell actin/myosin bands and cardiac specific gene expressions of β-MYH7 and SCN5A.1 and SCN5A.2 in both neonatal and adult cells. Additionally, upon exposure to variously spaced aligned fibers, adult CM action/myosin structure and morphology did not change but the overall orientation of the cells, relative to the fibers, increased from 45° to parallel as fiber spacing increased from 2 µm to 15µm. These findings provide critical insights into ECM-CM interactions that are responsible for maintenance/loss of neonatal and adult cardiomyocyte phenotype, and highlight the importance of developing more relevant cardiomyocyte culture substrates for in vitro studies.
dc.format.mimetypeapplication/pdf
dc.subjectelectrospun scaffold
dc.subjectcardiomyocyte phenotype
dc.subjectextracellular matrix
dc.titleCardiac ECM Structure-Mimetic Electrospun Scaffolds Reinstate Healthy Cardiomyocyte Phenotype
dc.typethesis
dc.contributor.committeeMemberDouglas B. Sawyer, M.D., Ph.D.
dc.type.materialtext
thesis.degree.nameMS
thesis.degree.levelthesis
thesis.degree.disciplineBiomedical Engineering
thesis.degree.grantorVanderbilt University
local.embargo.terms2014-07-26
local.embargo.lift2014-07-26
dc.contributor.committeeChairHak-Joon Sung, Ph.D.


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