SINGLE-CELL LEVEL INVESTIGATION OF CYTOSKELETAL/CELLULAR RESPONSE TO EXTERNAL STIMULI

Hiddessen, A L

关键词: ADHESIVES;    BIOLOGICAL FUNCTIONS;    CALIFORNIA;    DISEASES;    FLUORESCENCE;    GLASS;    IN VITRO;    MICROSCOPY;    POLYMERS;    PROTEINS;    SILICON;    STEM CELLS;    STIMUL;   

DOI  :  10.2172/902301
RP-ID  :  UCRL-TR-228478
PID  :  OSTI ID: 902301
Others  :  TRN: US200717%%528

美国|英语

来源: SciTech Connect

【 摘 要 】

A detailed understanding of the molecular mechanisms by which chemical signals control cell behavior is needed if the complex biological processes of embryogenesis, development, health and disease are to be completely understood. Yet, if we are to fully understand the molecular mechanisms controlling cell behavior, measurements at the single cell level are needed to supplement information gained from population level studies. One of the major challenges to accomplishing studies at the single cell level has been a lack of physical tools to complement the powerful molecular biological assays which have provided much of what we currently know about cell behavior. The goal of this exploratory project is the development of an experimental platform that facilitates integrated observation, tracking and analysis of the responses of many individual cells to controlled environmental factors (e.g. extracellular signals). Toward this goal, we developed chemically-patterned microarrays of both adherent and suspension mammalian cell types. A novel chemical patterning methodology, based on photocatalytic lithography, was developed to construct biomolecule and cell arrays that facilitate analysis of biological function. Our patterning techniques rely on inexpensive stamp materials and visible light, and do not necessitate mass transport or specified substrates. Patterned silicon and glass substrates are modified such that there is a non-biofouling polymer matrix surrounding the adhesive regions that target biomolecules and cells. Fluorescence and reflectance microscopy reveal successful patterning of proteins and single to small clusters of mammalian cells. In vitro assays conducted upon cells on the patterned arrays demonstrate the viability of cells interfacing with this synthetic system. Hence, we have successfully established a versatile cell measurement platform which can be used to characterize the molecular regulators of cellular behavior in a variety of important biological processes. The achievements realized in this project have enabled presentations and publication within the international scientific community, new collaborations with researchers at the University of California, and successful competition for three additional, separate research grants on studies of stem cell fate commitment and pathogen-host cell interactions.