-
Keynote Speaker - Robotic FluidFM in the Nanobiosensorics Lab: from large-area printing to high-throughput adhesion and injection of single cells - Session Mechanobiology
Dr. Robert HorvathDone
-
Online - FluidFM – A versatile method in biomaterials research - Session Material Sciences
Dr. Christine Müller-RennoDone
-
Registration & Coffee Break
Done
-
Keynote Speaker: Evaluation of FluidFM technology for single-cell genome editing - Session - Genome Engineering
Dr. Simona PatangeDone
-
Engineering Endosymbiotic Growth of E. coli in Mammalian Cells - Session Genome Engineering
Chantal ErnstDone
-
Quantification of micro/nano objects movement under vortex force by Fluidic Force Microscopy - Session Mechanobiology
Dr. Yonghui ZhangDone
-
Transient Changes in Stem Cells Induced by Electrical Stimulation - Session Mechanobiology
Dr. Amy GelmiDone
-
Lunch - Day2
Done
-
Registration & Coffee
Done
-
Lunch & Poster Session n*1
Done
Department of Chemistry, University of California, Davis, CA 95616, United States
Abstract
Single cell mechanics, derived from atomic force microscopy-based technology in conjunction with cellular imaging and assays, provides a new and effective means to measure the elastic compliance of cellular membrane, cytoskeleton, as well as nuclei. In addition, applying mechanical force to living cells could actively trigger and regulate the cellular signaling processes and ultimately allowing regulation of cellular behaviors. This presentation first introduces the technology, methodology, and latest developments to perform single cell mechanics in vitro, and to extract the cellular mechano-profiles qualitatively and quantitatively. Two applications will then be discussed: (a) using single cell mechanics as a readout for monitoring nanoparticle-cell interactions, as such nanocytotoxicity; and (b) using single cell mechanical perturbation to trigger and regulate cellular signaling and functions. The former reveals that single cell-based studies are a necessary and valuable tool to probe in-vivo pulmonary nanotoxicity. The latter opens a new pathway towards programming cellular signaling processing, e.g., by systematic variation of transient mechanical perturbation at the single cell level.
KEYWORDS: Atomic force microscopy | Single cell compression | Cell mechanics | Membrane blebbing | Mechano-sensing | Cell signaling