Mechanical Regulation of Oral Epithelial Barrier Function

Author:

Lee Eun-Jin123ORCID,Kim Yoontae1ORCID,Salipante Paul4,Kotula Anthony P.4ORCID,Lipshutz Sophie1ORCID,Graves Dana T.5,Alimperti Stella1

Affiliation:

1. Department of Biochemistry and Molecular & Cellular Biology, School of Medicine, Georgetown University, Washington, DC 20057, USA

2. Microsystems and Nanotechnology Division, Physical Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA

3. Department of Chemistry and Biochemistry, College of Computer, Mathematical and Natural Sciences, University of Maryland, College Park, MD 20742, USA

4. Materials Science and Engineering Division, Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA

5. Department of Periodontics, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA

Abstract

Epithelial cell function is modulated by mechanical forces imparted by the extracellular environment. The transmission of forces onto the cytoskeleton by modalities such as mechanical stress and matrix stiffness is necessary to address by the development of new experimental models that permit finely tuned cell mechanical challenges. Herein, we developed an epithelial tissue culture model, named the 3D Oral Epi-mucosa platform, to investigate the role mechanical cues in the epithelial barrier. In this platform, low-level mechanical stress (0.1 kPa) is applied to oral keratinocytes, which lie on 3D fibrous collagen (Col) gels whose stiffness is modulated by different concentrations or the addition of other factors such as fibronectin (FN). Our results show that cells lying on intermediate Col (3 mg/mL; stiffness = 30 Pa) demonstrated lower epithelial leakiness compared with soft Col (1.5 mg/mL; stiffness = 10 Pa) and stiff Col (6 mg/mL; stiffness = 120 Pa) gels, indicating that stiffness modulates barrier function. In addition, the presence of FN reversed the barrier integrity by inhibiting the interepithelial interaction via E-cadherin and Zonula occludens-1. Overall, the 3D Oral Epi-mucosa platform, as a new in vitro system, will be utilized to identify new mechanisms and develop future targets involved in mucosal diseases.

Funder

National Institute of Dental and Craniofacial Research (NIDCR) of the National Institutes of Health

NIH R01 Award

Professional Research Experience Program Agreement between the University of Maryland and the National Institute of Standards and Technology

Microscopy and Imaging Shared Resource (MISR) and the Lombardi Comprehensive Cancer Center

Publisher

MDPI AG

Subject

Bioengineering

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