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1.
Methods Cell Biol ; 83: 443-72, 2007.
Article in English | MEDLINE | ID: mdl-17613320

ABSTRACT

Analysis of how cells sense and respond to mechanical stress has been limited by the availability of techniques that can apply controlled mechanical forces to living cells while simultaneously measuring changes in cell and molecular distortion, as well as alterations of intracellular biochemistry. We have confronted this challenge by developing new engineering methods to measure and manipulate the mechanical properties of cells and their internal cytoskeletal and nuclear frameworks, and by combining them with molecular cell biological techniques that rely on microscopic analysis and real-time optical readouts of biochemical signaling. In this chapter, we describe techniques like microcontact printing, magnetic twisting cytometry, and magnetic pulling cytometry that can be systematically used to study the molecular basis of cellular mechanotransduction.


Subject(s)
Biomechanical Phenomena/methods , Cytological Techniques/instrumentation , Mechanotransduction, Cellular , Animals , Cattle , Cell Lineage , Cell Shape , Cytoskeleton , Electromagnetic Phenomena
2.
Biomaterials ; 28(17): 2783-90, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17339050

ABSTRACT

Development of biochips containing living cells for biodetection, drug screening and tissue engineering applications is limited by a lack of reconfigurable material interfaces and actuators. Here we describe a new class of nanostructured magnetizable materials created with a femtosecond laser surface etching technique that function as multiplexed magnetic field gradient concentrators. When combined with magnetic microbeads coated with cell adhesion ligands, these materials form microarrays of 'virtual' adhesive islands that can support cell attachment, resist cell traction forces and maintain cell viability. A cell death (apoptosis) response can then be actuated on command by removing the applied magnetic field, thereby causing cell retraction, rounding and detachment. This simple technology may be used to create reconfigurable interfaces that allow users to selectively discard contaminated or exhausted cellular sensor elements, and to replace them with new living cellular components for continued operation in future biomedical microdevices and biodetectors.


Subject(s)
Endothelial Cells/cytology , Magnetics , Nanostructures , Apoptosis , Biomechanical Phenomena , Cell Adhesion , Cell Death , Cell Shape , Cell Survival , Humans , Lasers , Microscopy, Fluorescence , Microspheres
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