Modeling the Maturation of the Vocal Fold Lamina Propria Using a Bioorthogonally Tunable Hydrogel Platform

Author(s)Zou, Xiaoyu
Author(s)Zhang, He
Author(s)Benson, Jamie M.
Author(s)Gao, Hanyuan
Author(s)Burris, David L.
Author(s)Fox, Joseph. M.
Author(s)Jia, Xinqiao
Date Accessioned2024-01-03T17:42:23Z
Date Available2024-01-03T17:42:23Z
Publication Date2023-08-02
Description© 2023 Wiley-VCH GmbH. This is the peer reviewed version of the following article: X. Zou, H. Zhang, J. M. Benson, H. Gao, D. L. Burris, J. M. Fox, X. Jia, Modeling the Maturation of the Vocal Fold Lamina Propria Using a Bioorthogonally Tunable Hydrogel Platform. Adv. Healthcare Mater. 2023, 12, 2301701. https://doi.org/10.1002/adhm.202301701, which has been published in final form at https://doi.org/10.1002/adhm.202301701. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited. This article will be embargoed until 08/13/2024.
AbstractToward the goal of establishing an engineered model of the vocal fold lamina propria (LP), mesenchymal stem cells (MSCs) are encapsulated in hyaluronic acid (HA)-based hydrogels employing tetrazine ligation with strained alkenes. To mimic matrix stiffening during LP maturation, diffusion-controlled interfacial bioorthogonal crosslinking is carried out on the soft cellular construct using HA modified with a ferocious dienophile, trans-cyclooctene (TCO). Cultures are maintained in MSC growth media for 14 days to afford a model of a newborn LP that is homogeneously soft (nLP), a homogeneously stiffened construct zero (sLP0) or 7 days (sLP7) post cell encapsulation, and a mature LP model (mLP) with a stiff top layer and a soft bottom layer. Installation of additional HA crosslinks restricts cell spreading. Compared to the nLP controls, sLP7 conditions upregulate the expression of fibrous matrix proteins (Col I, DCN, and FN EDA), classic fibroblastic markers (TNC, FAP, and FSP1), and matrix remodeling enzymes (MMP2, TIMP1, and HAS3). Day 7 stiffening also upregulates the catabolic activities, enhances ECM turnover, and promotes YAP expression. Overall, in situ delayed matrix stiffening promotes a fibroblast transition from MSCs and enhances YAP-regulated mechanosensing.
SponsorX.Z. and H.Z. contributed equally to this work. This work was supported in part by the National Institutes of Health (NIDCD, R01DC014461; NIDCR R01DE029655), National Science Foundation (NSF, DMR-2243648), and Delaware Bioscience Center for Advanced Technology (DE-CAT). Instrumentation and core facility support was made possible by NIH (S10 OD016361, P20GM103446, P20GM139760) and NSF (CHE-0840401, CHE-1229234, IIA-1301765) grants. The authors also acknowledge the use of facilities and instrumentation supported by NSF through the University of Delaware Materials Research Science and Engineering Center (DMR-2011824).
CitationX. Zou, H. Zhang, J. M. Benson, H. Gao, D. L. Burris, J. M. Fox, X. Jia, Modeling the Maturation of the Vocal Fold Lamina Propria Using a Bioorthogonally Tunable Hydrogel Platform. Adv. Healthcare Mater. 2023, 12, 2301701. https://doi.org/10.1002/adhm.202301701
ISSN2192-2659
URLhttps://udspace.udel.edu/handle/19716/33759
Languageen_US
PublisherAdvanced Healthcare Materials
Keywordshyaluronic acids
Keywordsmatrix stiffening
Keywordsmesenchymal stem cells
Keywordstetrazine ligations
Keywordsvocal folds
TitleModeling the Maturation of the Vocal Fold Lamina Propria Using a Bioorthogonally Tunable Hydrogel Platform
TypeArticle
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