The vocal fold (VF) mucosa is a complex layered structure comprised of a squamous cell epithelium, basement membrane and lamina propria rich in extracellular matrix (ECM). Each mucosal layer holds a distinct set of functions that are together responsible for VF immune, transport and barrier capabilities, an ability to absorb considerable impact stress, and favorable viscoelastic properties allowing self-sustained tissue oscillation for voice production. Disruption or destruction of the VF mucosa due to trauma or disease has severe consequences for VF oscillation and generally results in a refractory dysphonia. Previous work in the area of VF tissue repair and regeneration has focused on homogenous biomaterials, individual cell populations, and individual or small groups of genes/proteins;however, these approaches are inadequate in attempting to reconstruct the inherent complexity of this dynamic biological and biomechanical system. A clinically meaningful approach to the replacement of large VF mucosal deficits requires a tissue engineering strategy that incorporates a layered structure, sophisticated ECM network and multiple cell types. The proposed research directly confronts these challenges by focusing on the optimization of a multi-layered VF mucosa substitute based on decellularized VF ECM and coculture of VF fibroblasts and keratinocytes. We will conduct this research using a novel combination of tissue engineering, cellular and molecular biology, proteomic/glycomic, and functional vibratory techniques;allowing us to directly evaluate cell behavior, the system-wide status of the entire ECM protein and glycan network, and the oscillatory potential of these engineered structures compared with native VF tissue. Understanding the dynamics of matrix turnover, cell- ECM interaction, and vibratory performance in a controlled in vitro environment is critical to optimizing this tissue engineering approach for future in vivo experiments and eventual clinical implementation. In addition to achieving these therapeutically driven goals, the proposed research will significantly improve understanding of the native VF mucosa at the proteomic and glycomic levels, and introduce a VF organotypic coculture model with wide-ranging applicability to the study of VF epithelial morphogenesis and development, physiologic, immunologic and barrier function.

Public Health Relevance

The vocal fold mucosa is a complex biological structure that underpins normal voice production. The proposed research is focused on the optimization of a multi-layered vocal fold mucosa substitute for the treatment of diseased or damaged tissue, and restoration of vocal function.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
1R01DC010777-01
Application #
7863445
Study Section
Motor Function, Speech and Rehabilitation Study Section (MFSR)
Program Officer
Shekim, Lana O
Project Start
2010-04-01
Project End
2015-03-31
Budget Start
2010-04-01
Budget End
2011-03-31
Support Year
1
Fiscal Year
2010
Total Cost
$499,050
Indirect Cost
Name
University of Wisconsin Madison
Department
Surgery
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Li, Qiyao; Shortreed, Michael R; Wenger, Craig D et al. (2017) Global Post-Translational Modification Discovery. J Proteome Res 16:1383-1390
Thibeault, Susan L; Welham, Nathan V (2017) Strategies for advancing laryngeal tissue engineering. Laryngoscope 127:2319-2320
Gilpin, Sarah E; Li, Qiyao; Evangelista-Leite, Daniele et al. (2017) Fibrillin-2 and Tenascin-C bridge the age gap in lung epithelial regeneration. Biomaterials 140:212-219
Moore, Jaime E; Rathouz, Paul J; Havlena, Jeffrey A et al. (2016) Practice variations in voice treatment selection following vocal fold mucosal resection. Laryngoscope 126:2505-2512
Li, Qiyao; Chang, Zhen; Oliveira, Gisele et al. (2016) Protein turnover during in vitro tissue engineering. Biomaterials 81:104-113
Kishimoto, Ayami Ohno; Kishimoto, Yo; Young, David L et al. (2016) High- and ultrahigh-field magnetic resonance imaging of naïve, injured and scarred vocal fold mucosae in rats. Dis Model Mech 9:1397-1403
Kishimoto, Yo; Kishimoto, Ayami Ohno; Ye, Shuyun et al. (2016) Modeling fibrosis using fibroblasts isolated from scarred rat vocal folds. Lab Invest 96:807-16
Li, Qiyao; Uygun, Basak E; Geerts, Sharon et al. (2016) Proteomic analysis of naturally-sourced biological scaffolds. Biomaterials 75:37-46
Ling, Changying; Li, Qiyao; Brown, Matthew E et al. (2015) Bioengineered vocal fold mucosa for voice restoration. Sci Transl Med 7:314ra187
Welham, Nathan V; Ling, Changying; Dawson, John A et al. (2015) Microarray-based characterization of differential gene expression during vocal fold wound healing in rats. Dis Model Mech 8:311-21

Showing the most recent 10 out of 16 publications