Boron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.

In this paper, we describe the effects of the combination of topographical, mechanical, chemical and intracellular electrical stimuli on a co-culture of fibroblasts and skeletal muscle cells. The co-culture was anisotropically grown onto an engineered micro-grooved (10 µm-wide grooves) polyacrylamid...

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Autores principales: Leonardo Ricotti, Toshinori Fujie, Helena Vazão, Gianni Ciofani, Roberto Marotta, Rosaria Brescia, Carlo Filippeschi, Irene Corradini, Michela Matteoli, Virgilio Mattoli, Lino Ferreira, Arianna Menciassi
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spelling oai:doaj.org-article:017e46c068c24723a75e2387d3bc32242021-11-18T08:59:34ZBoron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.1932-620310.1371/journal.pone.0071707https://doaj.org/article/017e46c068c24723a75e2387d3bc32242013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23977119/?tool=EBIhttps://doaj.org/toc/1932-6203In this paper, we describe the effects of the combination of topographical, mechanical, chemical and intracellular electrical stimuli on a co-culture of fibroblasts and skeletal muscle cells. The co-culture was anisotropically grown onto an engineered micro-grooved (10 µm-wide grooves) polyacrylamide substrate, showing a precisely tuned Young's modulus (∼ 14 kPa) and a small thickness (∼ 12 µm). We enhanced the co-culture properties through intracellular stimulation produced by piezoelectric nanostructures (i.e., boron nitride nanotubes) activated by ultrasounds, thus exploiting the ability of boron nitride nanotubes to convert outer mechanical waves (such as ultrasounds) in intracellular electrical stimuli, by exploiting the direct piezoelectric effect. We demonstrated that nanotubes were internalized by muscle cells and localized in both early and late endosomes, while they were not internalized by the underneath fibroblast layer. Muscle cell differentiation benefited from the synergic combination of topographical, mechanical, chemical and nanoparticle-based stimuli, showing good myotube development and alignment towards a preferential direction, as well as high expression of genes encoding key proteins for muscle contraction (i.e., actin and myosin). We also clarified the possible role of fibroblasts in this process, highlighting their response to the above mentioned physical stimuli in terms of gene expression and cytokine production. Finally, calcium imaging-based experiments demonstrated a higher functionality of the stimulated co-cultures.Leonardo RicottiToshinori FujieHelena VazãoGianni CiofaniRoberto MarottaRosaria BresciaCarlo FilippeschiIrene CorradiniMichela MatteoliVirgilio MattoliLino FerreiraArianna MenciassiPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 8, p e71707 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Leonardo Ricotti
Toshinori Fujie
Helena Vazão
Gianni Ciofani
Roberto Marotta
Rosaria Brescia
Carlo Filippeschi
Irene Corradini
Michela Matteoli
Virgilio Mattoli
Lino Ferreira
Arianna Menciassi
Boron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.
description In this paper, we describe the effects of the combination of topographical, mechanical, chemical and intracellular electrical stimuli on a co-culture of fibroblasts and skeletal muscle cells. The co-culture was anisotropically grown onto an engineered micro-grooved (10 µm-wide grooves) polyacrylamide substrate, showing a precisely tuned Young's modulus (∼ 14 kPa) and a small thickness (∼ 12 µm). We enhanced the co-culture properties through intracellular stimulation produced by piezoelectric nanostructures (i.e., boron nitride nanotubes) activated by ultrasounds, thus exploiting the ability of boron nitride nanotubes to convert outer mechanical waves (such as ultrasounds) in intracellular electrical stimuli, by exploiting the direct piezoelectric effect. We demonstrated that nanotubes were internalized by muscle cells and localized in both early and late endosomes, while they were not internalized by the underneath fibroblast layer. Muscle cell differentiation benefited from the synergic combination of topographical, mechanical, chemical and nanoparticle-based stimuli, showing good myotube development and alignment towards a preferential direction, as well as high expression of genes encoding key proteins for muscle contraction (i.e., actin and myosin). We also clarified the possible role of fibroblasts in this process, highlighting their response to the above mentioned physical stimuli in terms of gene expression and cytokine production. Finally, calcium imaging-based experiments demonstrated a higher functionality of the stimulated co-cultures.
format article
author Leonardo Ricotti
Toshinori Fujie
Helena Vazão
Gianni Ciofani
Roberto Marotta
Rosaria Brescia
Carlo Filippeschi
Irene Corradini
Michela Matteoli
Virgilio Mattoli
Lino Ferreira
Arianna Menciassi
author_facet Leonardo Ricotti
Toshinori Fujie
Helena Vazão
Gianni Ciofani
Roberto Marotta
Rosaria Brescia
Carlo Filippeschi
Irene Corradini
Michela Matteoli
Virgilio Mattoli
Lino Ferreira
Arianna Menciassi
author_sort Leonardo Ricotti
title Boron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.
title_short Boron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.
title_full Boron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.
title_fullStr Boron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.
title_full_unstemmed Boron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.
title_sort boron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/017e46c068c24723a75e2387d3bc3224
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