At a fundamental level, advances in biomaterials research are driven by the ability to elicit desired cell behaviors through the development of instructive biomaterial surfaces. Rational design of novel biomaterials that can successfully manipulate cell behavior toward a specific function requires both identification of instructive cues and a mechanistic understanding of how these cues alter cellular function. However, determining the specific combination of cues to induce a precise set of cellular behaviors leading to a predictable functional outcome remains challenging. The challenge stems from an incomplete understanding of the mechanisms used by cells to detect and respond to environmental cues, particularly physical cues such as confinement of cell shape or stiffness of the extracellular environment. Physical cues are detected through mechanotransduction, a poorly understood process through which cells convert physical stimuli into biochemically detectable signals. Recent advances in the study of mechanotransduction have isolated a key role for the focal adhesion protein vinculin, an important linkage in the mechanical connections between the extracellular environment and the force-generating actin cytoskeleton. This proposal seeks to evaluate the hypothesis that cells sense diverse changes in the physical nature of the cell-biomaterial interface through distinct mechanical loading of vinculin, leading to the activation of cell signaling pathways. Specifically, we will study the effects of cell shape, cell size, and extracellular proteins on force-sensitive signal activation. The proposed work is relevant to the mission of NIH as it will increase the fundamental understanding of how cells sense and respond to the physical aspects of their surroundings. This will lay the foundation for advances in biomaterials design as well as aid efforts to understand disease states associated with defects in the physical nature of the cellular environment, such as cancer and excessive tissue fibrosis.

Public Health Relevance

At a fundamental level, advances in biomaterials research are driven by the ability to elicit desired cell behaviors through the development of instructive biomaterial surfaces. While powerful approaches have been developed for incorporating instructive cues into materials, there is limited understanding of the cell signaling pathways that are important in the detection and response to these stimuli, particularly in the case of physical cues. The proposed work is relevant to the mission of the NIH because it will increase the fundamental understanding of how cells sense and respond to the physical aspects of their surroundings, which will lay the foundation for advances in biomaterials design as well as aid research regarding disease states impacted by physical cues from the in vivo environment, such as excessive tissue fibrosis and cancer.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21EB022166-01A1
Application #
9245194
Study Section
Biomaterials and Biointerfaces Study Section (BMBI)
Program Officer
Hunziker, Rosemarie
Project Start
2016-09-01
Project End
2018-06-30
Budget Start
2016-09-01
Budget End
2017-06-30
Support Year
1
Fiscal Year
2016
Total Cost
$226,319
Indirect Cost
$76,319
Name
Duke University
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Pomeroy, Jordan E; Nguyen, Hung X; Hoffman, Brenton D et al. (2017) Genetically Encoded Photoactuators and Photosensors for Characterization and Manipulation of Pluripotent Stem Cells. Theranostics 7:3539-3558