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Extracellular Matrix Physical Properties Alter Cell Mechanics, Morphology, and Proliferation - Disquisitiones Mechanicae Seminar Series

Event Type
Professor Taher Saif
NCSA Auditorium
Nov 7, 2013   4:00 - 5:00 pm  
Professor Paul Janmey, University of Pennsylvania
Debbie Richardson
Originating Calendar
MechSE Seminars


Many cell types are sensitive to mechanical signals that are produced either by application of exogenous force to their surfaces or by the resistance that their surroundings place on forces generated by the cells themselves.  Cell morphology, motility, proliferation, and protein expression all change in response to substrate stiffness.  The range of stiffness over which different primary cell types respond can vary over a wide range and generally reflects the elastic modulus of the tissue from which these cells were isolated.  Mechanosensing depends on the type of adhesion receptor by which the cell binds, and therefore on both the molecular composition of the extracellular matrix and the nature of its link to the cytoskeleton.  Many cell types can alter their own stiffness to match that of the substrate to which they adhere.  The maximal elastic modulus that cells such as fibroblasts can attain is similar to that of crosslinked actin networks at the concentrations in the cell cortex. Simultaneous control of substrate stiffness and adhesive patterns suggests that stiffness sensing occurs on a length scale much larger than single molecular linkages and that the time needed for mechanosensing is on the order of a few seconds.

About the Speaker

Paul Janmey is Professor of Physiology, Physics, and Bioengineering at the Institute of Medicine and Engineering at the University of Pennsylvania.  He received his Ph.D. in physical chemistry from the University of Wisconsin and completed his postdoc at the Hematology-Oncology Unit at Massachusetts General Hospital.   Dr. Janmey’s research interests include the interaction between cytoskeletal and extracellular matrix stiffness, effects of substrate mechanics on cell structure and function, phosphoinositide signaling for actin assembly, fibrin-based materials for wound healing, and intermediate filament assembly and mechanics.

* Times, dates and titles are subject to change.  Check for updated information.  This seminar counts toward the requirements for ME 590 and TAM 500.                     

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