Characterization of intrauterine growth, proliferation and biomechanical properties of the murine larynx.

Current research approaches employ traditional tissue engineering strategies to promote vocal fold (VF) tissue regeneration, whereas recent novel advances seek to use principles of developmental biology to guide tissue generation by mimicking native developmental cues, causing tissue or allogenic/au...

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Main Authors: Kate Griffin, Hailey Pedersen, Kari Stauss, Vlasta Lungova, Susan L Thibeault
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0245073
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spelling doaj-5b65995508204e06a52914b3a9954cc72021-05-13T04:30:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01161e024507310.1371/journal.pone.0245073Characterization of intrauterine growth, proliferation and biomechanical properties of the murine larynx.Kate GriffinHailey PedersenKari StaussVlasta LungovaSusan L ThibeaultCurrent research approaches employ traditional tissue engineering strategies to promote vocal fold (VF) tissue regeneration, whereas recent novel advances seek to use principles of developmental biology to guide tissue generation by mimicking native developmental cues, causing tissue or allogenic/autologous progenitor cells to undergo the regeneration process. To address the paucity of data to direct VF differentiation and subsequent new tissue formation, we characterize structure-proliferation relationships and tissue elastic moduli over embryonic development using a murine model. Growth, cell proliferation, and tissue biomechanics were taken at E13.5, E15.5, E16.5, E18.5, P0, and adult time points. Quadratic growth patterns were found in larynx length, maximum transverse diameter, outer dorsoventral diameter, and VF thickness; internal VF length was found to mature linearly. Cell proliferation measured with EdU in the coronal and transverse planes of the VFs was found to decrease with increasing age. Exploiting atomic force microscopy, we measured significant differences in tissue stiffness across all time points except between E13.5 and E15.5. Taken together, our results indicate that as the VF mature and develop quadratically, there is a concomitant tissue stiffness increase. Greater gains in biomechanical stiffness at later prenatal stages, correlated with reduced cell proliferation, suggest that extracellular matrix deposition may be responsible for VF thickening and increased biomechanical function, and that the onset of biomechanical loading (breathing) may also contribute to increased stiffness. These data provide a profile of VF biomechanical and growth properties that can guide the development of biomechanically-relevant scaffolds and progenitor cell differentiation for VF tissue regeneration.https://doi.org/10.1371/journal.pone.0245073
collection DOAJ
language English
format Article
sources DOAJ
author Kate Griffin
Hailey Pedersen
Kari Stauss
Vlasta Lungova
Susan L Thibeault
spellingShingle Kate Griffin
Hailey Pedersen
Kari Stauss
Vlasta Lungova
Susan L Thibeault
Characterization of intrauterine growth, proliferation and biomechanical properties of the murine larynx.
PLoS ONE
author_facet Kate Griffin
Hailey Pedersen
Kari Stauss
Vlasta Lungova
Susan L Thibeault
author_sort Kate Griffin
title Characterization of intrauterine growth, proliferation and biomechanical properties of the murine larynx.
title_short Characterization of intrauterine growth, proliferation and biomechanical properties of the murine larynx.
title_full Characterization of intrauterine growth, proliferation and biomechanical properties of the murine larynx.
title_fullStr Characterization of intrauterine growth, proliferation and biomechanical properties of the murine larynx.
title_full_unstemmed Characterization of intrauterine growth, proliferation and biomechanical properties of the murine larynx.
title_sort characterization of intrauterine growth, proliferation and biomechanical properties of the murine larynx.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description Current research approaches employ traditional tissue engineering strategies to promote vocal fold (VF) tissue regeneration, whereas recent novel advances seek to use principles of developmental biology to guide tissue generation by mimicking native developmental cues, causing tissue or allogenic/autologous progenitor cells to undergo the regeneration process. To address the paucity of data to direct VF differentiation and subsequent new tissue formation, we characterize structure-proliferation relationships and tissue elastic moduli over embryonic development using a murine model. Growth, cell proliferation, and tissue biomechanics were taken at E13.5, E15.5, E16.5, E18.5, P0, and adult time points. Quadratic growth patterns were found in larynx length, maximum transverse diameter, outer dorsoventral diameter, and VF thickness; internal VF length was found to mature linearly. Cell proliferation measured with EdU in the coronal and transverse planes of the VFs was found to decrease with increasing age. Exploiting atomic force microscopy, we measured significant differences in tissue stiffness across all time points except between E13.5 and E15.5. Taken together, our results indicate that as the VF mature and develop quadratically, there is a concomitant tissue stiffness increase. Greater gains in biomechanical stiffness at later prenatal stages, correlated with reduced cell proliferation, suggest that extracellular matrix deposition may be responsible for VF thickening and increased biomechanical function, and that the onset of biomechanical loading (breathing) may also contribute to increased stiffness. These data provide a profile of VF biomechanical and growth properties that can guide the development of biomechanically-relevant scaffolds and progenitor cell differentiation for VF tissue regeneration.
url https://doi.org/10.1371/journal.pone.0245073
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AT karistauss characterizationofintrauterinegrowthproliferationandbiomechanicalpropertiesofthemurinelarynx
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