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Volume 142, Issue 2, Pages 191-195 (February 2010)


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Lumen formation in three-dimensional cultures of salivary acinar cells

This article was presented at the 2009 AAO–HNSF Annual Meeting & OTO EXPO, San Diego, CA, October 4-7, 2009.

Swati Pradhanab, Chao Liu, PhDc, Chu Zhang, PhDab, Xinqiao Jia, PhDbc, Mary C. Farach-Carson, PhDabe, Robert L. Witt, MDbdfCorresponding Author Informationemail address

Received 10 September 2009; accepted 27 October 2009.

Abstract 

Objective

Development of an artificial salivary gland will benefit patients with xerostomia after radiation therapy for upper respiratory cancer. The goal is to devise a three-dimensional (3D) culture system in which salivary cells differentiate into polarized acini that express essential biomarkers and directionally secrete α-amylase. Differentiated acini-like structures in a 3D biomaterial-based scaffold will mimic salivary gland functions.

Study Design

Cells were seeded onto HA-based hydrogels containing PlnDIV peptide and allowed to differentiate into acini-like structures. Cell viability and phenotype were examined.

Setting

Laboratory-based tissue procurement study.

Subjects and Methods

Salivary gland tissue was obtained from patients undergoing surgery. Marker expression established the phenotype of salivary gland cells. Perlecan/HSPG2, an important component of the basement membrane, was highly expressed in salivary gland tissue. A culture system consisting of hyaluronic acid (HA) hydrogel and a coupled bioactive peptide derived from domain IV of perlecan (PlnDIV) was used. Prior studies demonstrated differentiation of acinar cells into lobular structures that mimicked intact glands when cultured on PlnDIV peptide–coated surfaces.

Results

Lobular acini-like structures formed on hydrogels and expressed tight junction components such as zona occludens 1. Acini-like structures were stained for the presence of α-amylase. Live/dead staining revealed the presence of apoptotic cells in the center of the acini-like structures, indicative of lumen formation.

Conclusion

A novel system supporting acini-like assembly in a 3D culture system was established. Presence of biomarkers and secretion of salivary enzymes confirms functionality in vitro. Future experiments will test the 3D system in an animal model.

a Department of Biological Sciences, University of Delaware, Newark, DE

b Center for Translational Cancer Research, University of Delaware, Newark, DE

c Department of Materials Sciences and Engineering, University of Delaware, Newark, DE

d Christiana Care Health Systems, Newark, DE

e Biochemistry and Cell Biology, Rice University, Houston, TX

f Jefferson Medical College, Philadelphia, PA

Corresponding Author InformationCorresponding author: Robert L. Witt, MD, Christiana Hospital, Medical Arts Pavilion 1-Suite 112,4745 Ogletown-Stanton Rd, Newark DE 19713-2070

 Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.

PII: S0194-5998(09)01659-3

doi:10.1016/j.otohns.2009.10.039


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