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Mechanobiology of Disease

Poster Abstracts

120

63-POS

Board 63

Atomic Force Microscopy as Tool to Selectively Investigate the Mehcanical Properties of

Different Components of Cytoskeleton in Muscle Fibres in Vitro

Roberto Raiteri

1

, Mariateresa Tedesco

1

, Ilaria Pulsoni

1

, Christopher Ward

2

.

1

University of Genova, Genova, Italy,

2

University of Maryland, School of Medicine, Baltimore,

MD, USA.

Atomic force microscopy (AFM) allows to measure the transversal stiffness of the sub-

sarcolemma region of cells with sub-micrometer lateral and vertical resolution. By AFM

nanoindentation measurements we investigated the changes in stiffness of isolated skeletal

muscle fibres induced by acute doses of different substances capable to selectively induce

changes in the organization of microtubules and intermediate filaments, namely colchicine, taxol,

parthenolide, and Withaferin A. Our results confirm that AFM nanoindentation performed at

different penetration depths allows to selectively and quantitatively probe the response of

different regions of the sarcolemma localized in the first few hundreds of nanometers below the

sarcolemma. Such capability represents a powerful tool, complementary to other in vitro and in

vivo techniques, to investigate the mechano-transduction at the basis of generation and

progression muscle pathologies such as dystrophies.

66-POS

Board 66

Nanoscale Optomechanical Actuators for Controlling Mechanotransduction in Living Cells

Khalid Salaita

1,2

, Zheng Liu

1

,

Victor Ma

1

.

1

Emory University, Atlanta, GA, USA,

2

Emory University and Georgia Institute of Technology,

Atlanta, GA, USA.

Optical approaches for the controlling biological systems are transforming the field of cell

biology, as exemplified by caged or photoswitchable molecules and by optogenetic constructs.

Similarly, methods to harness light for delivering precise physical inputs to biological systems

could potentially transform the study of mechanotransduction. Toward this goal, I will describe

our efforts aimed at developing optomechanical actuator nanoparticles to manipulate receptor

mechanics with high spatiotemporal resolution using near-infrared illumination (Nature Methods

2016). Nanoparticles are comprised of a gold nanorod coated with a thermoresponsive polymer

shell. Illumination leads to local heating, and particle collapse, thus delivering piconewton forces

to specific cell surface receptors with high spatial (~micron scale) and temporal resolution (msec

timescales). Optomechanical actuators were used to exert forces through the integrin receptors,

thus mechanically controlling focal adhesion formation, cell protrusion, and cell migration in

living cells. This new approach to controlling mechanotransduction circuits allows for optically

controlling cell migration without the use of genetic engineering.