Millions of people suffer from xerostomia, or "dry mouth" resulting from lack of saliva, causing a decreased quality of life resulting from multiple symptoms, including increased dental caries, oropharyngeal infections, difficulties with swallowing (dysphagia) and digestion (mucositis), loss of taste, and pain. As current treatments for these problems are inadequate (1), there is considerable interest in creating an artificial salivary gland. Maintenance of salivary acinar cell differentiation and function in vitro is criticl to the successful engineering of such constructs;however, this breakthrough has not yet been achieved. This is primarily due to the current lack of basic scientific knowledge regarding the specific extracellular signals that are required to maintain or induce acinar cell differentiation, which remains a substantial limitation in the ability to engineer a functional artificial salivary gland. An in vitro assay system is needed to identify required extracellular signals. We hypothesize that the combination of chemically-modified nanofibers presented to cells via microscale patterning in a 3D scaffold will support salivary acinar cell function. This application proposes an innovative, interdisciplinary strategy to create a high-throughput, non-invasive assay system that will be used to sense salivary acinar cell secretory function in live cells grown on scaffold materials, which has not been previously possible. A MEMS-based saliva sensor will be produced to accurately measure the concentration of a salivary secretory protein secreted by cells grown on unique scaffold combinations. A novel multiplexed immunocytochemistry method will be used to assess the extent of differentiation in fixed cells following the biosensor assay. Using an innovative combination of methods, nanotopography, micropatterning, and chemical signaling will be independently modulated, such that specific combinations of parameters will be identified that support acinar cell function. Scaffolds will be assessed for their ability to maintin acinar differentiation or promote re-differentiation using a combination of primary cells and cell lines. We will address this hypothesis in four specific aims:
Aim 1 : Develop a high-throughput MEMS probe array assay system to evaluate acinar cell function in vitro.
Aim 2 : Identify the ideal nanofiber configuration to support salivary acinar cell differentiation.
Aim 3 : Optimize nanofiber surface properties to enhance salivary gland acinar cell function.
Aim 4 : Identify an optimal microtopography to promote acinar cell function. The in vitro salivary gland construct produced in this application will be useful to identify pathways regulating acinar function and can be applied for drug screening. The principles developed as a result of this application will be applied in the future towards engineering of artificial glands designed to replicate salivary gland and other complex branching organs.

Public Health Relevance

In this application, optimized micropatterned scaffolds having a nanofiber-coated surface will be engineered to develop a "smart" scaffold for functional saliva-secreting salivary gland acinar cells. The methods developed here will be useful for application in high-throughput drug screening. This work will be applied in the future to develop an orally implantable device to enhance salivary flow in patients suffering from salivary hypofunction.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
1R01DE022467-01A1
Application #
8373442
Study Section
Oral, Dental and Craniofacial Sciences Study Section (ODCS)
Program Officer
Lumelsky, Nadya L
Project Start
2012-07-01
Project End
2017-06-30
Budget Start
2012-07-01
Budget End
2013-06-30
Support Year
1
Fiscal Year
2012
Total Cost
$495,345
Indirect Cost
$165,313
Name
State University of New York at Albany
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
152652822
City
Albany
State
NY
Country
United States
Zip Code
12222
Dhulekar, Nimit; Ray, Shayoni; Yuan, Daniel et al. (2016) Prediction of Growth Factor-Dependent Cleft Formation During Branching Morphogenesis Using A Dynamic Graph-Based Growth Model. IEEE/ACM Trans Comput Biol Bioinform 13:350-64
Kwon, Hae Ryong; Larsen, Melinda (2015) The contribution of specific cell subpopulations to submandibular salivary gland branching morphogenesis. Curr Opin Genet Dev 32:47-54
Peters, Sarah B; Nelson, Deirdre A; Kwon, Hae Ryong et al. (2015) TGFβ signaling promotes matrix assembly during mechanosensitive embryonic salivary gland restoration. Matrix Biol 43:109-24
Nelson, Deirdre A; Larsen, Melinda (2015) Heterotypic control of basement membrane dynamics during branching morphogenesis. Dev Biol 401:103-9
Gervais, Elise M; Desantis, Kara A; Pagendarm, Nicholas et al. (2015) Changes in the Submandibular Salivary Gland Epithelial Cell Subpopulations During Progression of Sjögren's Syndrome-Like Disease in the NOD/ShiLtJ Mouse Model. Anat Rec (Hoboken) 298:1622-34
Mathew, Shomita S; Nieves, Bethsaida; Sequeira, Sharon et al. (2014) Integrins promote cytokinesis through the RSK signaling axis. J Cell Sci 127:534-45
Soscia, David A; Sequeira, Sharon J; Schramm, Robert A et al. (2013) Salivary gland cell differentiation and organization on micropatterned PLGA nanofiber craters. Biomaterials 34:6773-84
Cantara, Shraddha I; Soscia, David A; Sequeira, Sharon J et al. (2012) Selective functionalization of nanofiber scaffolds to regulate salivary gland epithelial cell proliferation and polarity. Biomaterials 33:8372-82