Literature DB >> 29305767

Finite element modeling to analyze TEER values across silicon nanomembranes.

Tejas S Khire1, Barrett J Nehilla1,2, Jirachai Getpreecharsawas1, Maria E Gracheva3, Richard E Waugh1, James L McGrath4.   

Abstract

Silicon nanomembranes are ultrathin, highly permeable, optically transparent and biocompatible substrates for the construction of barrier tissue models. Trans-epithelial/endothelial electrical resistance (TEER) is often used as a non-invasive, sensitive and quantitative technique to assess barrier function. The current study characterizes the electrical behavior of devices featuring silicon nanomembranes to facilitate their application in TEER studies. In conventional practice with commercial systems, raw resistance values are multiplied by the area of the membrane supporting cell growth to normalize TEER measurements. We demonstrate that under most circumstances, this multiplication does not 'normalize' TEER values as is assumed, and that the assumption is worse if applied to nanomembrane chips with a limited active area. To compare the TEER values from nanomembrane devices to those obtained from conventional polymer track-etched (TE) membranes, we develop finite element models (FEM) of the electrical behavior of the two membrane systems. Using FEM and parallel cell-culture experiments on both types of membranes, we successfully model the evolution of resistance values during the growth of endothelial monolayers. Further, by exploring the relationship between the models we develop a 'correction' function, which when applied to nanomembrane TEER, maps to experiments on conventional TE membranes. In summary, our work advances the the utility of silicon nanomembranes as substrates for barrier tissue models by developing an interpretation of TEER values compatible with conventional systems.

Entities:  

Keywords:  Coculture systems; Finite element analysis; Microfluidics; Silicon nanomembranes; Trans endothelial electrical resistance (TEER)

Mesh:

Substances:

Year:  2018        PMID: 29305767      PMCID: PMC5770343          DOI: 10.1007/s10544-017-0251-7

Source DB:  PubMed          Journal:  Biomed Microdevices        ISSN: 1387-2176            Impact factor:   2.838


  43 in total

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Journal:  Anal Chem       Date:  2010-03-15       Impact factor: 6.986

2.  Charge- and size-based separation of macromolecules using ultrathin silicon membranes.

Authors:  Christopher C Striemer; Thomas R Gaborski; James L McGrath; Philippe M Fauchet
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3.  A multiple-channel, multiple-assay platform for characterization of full-range shear stress effects on vascular endothelial cells.

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4.  An experimental and theoretical analysis of molecular separations by diffusion through ultrathin nanoporous membranes.

Authors:  J L Snyder; A Clark; D Z Fang; T R Gaborski; C C Striemer; P M Fauchet; J L McGrath
Journal:  J Memb Sci       Date:  2011-03-01       Impact factor: 8.742

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Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-11       Impact factor: 11.205

6.  Membrane Pore Spacing Can Modulate Endothelial Cell-Substrate and Cell-Cell Interactions.

Authors:  Stephanie M Casillo; Ana P Peredo; Spencer J Perry; Henry H Chung; Thomas R Gaborski
Journal:  ACS Biomater Sci Eng       Date:  2017-02-16

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Journal:  J Cell Biol       Date:  2014-02-03       Impact factor: 10.539

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4.  TRA2A-induced upregulation of LINC00662 regulates blood-brain barrier permeability by affecting ELK4 mRNA stability in Alzheimer's microenvironment.

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5.  Microvascular Mimetics for the Study of Leukocyte-Endothelial Interactions.

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