Principal Investigator

Davide Randazzo, Ph.D.

Dr. Davide Randazzo did his postdoctoral training at the University of Siena, Italy, where he characterized a mouse model knockout for the muscle protein obscurin. He moved to the U.S. in 2014, for a position as a visiting fellow at the NIAMS.


The principal mission of the Light Imaging Section is to give NIAMS scientists access to state-of-the-art equipment and to offer training and assistance in the acquisition and analysis of high quality scientific images by light microscopy. Furthermore, we use light microscopy and other techniques to elucidate poorly understood aspects of skeletal muscle cell biology, i.e. the organization of muscle microtubules and their role in muscle diseases. We also strive to apply new modalities of light microscopy to the quantitative analysis of skeletal muscle pathologies.


The Light Imaging Section is equipped for widefield and confocal microscopy, multi-photon microscopy, TIRF, high-throughput live cell imaging, and slide scanning. See full list of instruments available.

For access to instruments and more information, contact Dr. Randazzo (davide.randazzo@nih.gov) or Ms. Kenea (aster.kenea@nih.gov).

Image & Media Gallery

Scientific Publications



A High-Throughput Real-Time Imaging Technique To Quantify NETosis and Distinguish Mechanisms of Cell Death in Human Neutrophils.

Gupta S, Chan DW, Zaal KJ, Kaplan MJ
Journal of immunology (Baltimore, Md. : 1950).
2018 Jan 15;
doi: 10.4049/jimmunol.1700905
PMID: 29196457

Clearing skeletal muscle with CLARITY for light microscopy imaging.

Milgroom A, Ralston E
Cell biology international.
2016 Apr;
doi: 10.1002/cbin.10578
PMID: 26732743

A new directionality tool for assessing microtubule pattern alterations.

Liu W, Ralston E
Cytoskeleton (Hoboken, N.J.).
2014 Apr;
doi: 10.1002/cm.21166
PMID: 24497496

Molecular editing of cellular responses by the high-affinity receptor for IgE.

Suzuki R, Leach S, Liu W, Ralston E, Scheffel J, Zhang W, Lowell CA, Rivera J
Science (New York, N.Y.).
2014 Feb 28;
doi: 10.1126/science.1246976
PMID: 24505132

Microtubules that form the stationary lattice of muscle fibers are dynamic and nucleated at Golgi elements.

Oddoux S, Zaal KJ, Tate V, Kenea A, Nandkeolyar SA, Reid E, Liu W, Ralston E
The Journal of cell biology.
2013 Oct 28;
doi: 10.1083/jcb.201304063
PMID: 24145165

Quantitative evaluation of skeletal muscle defects in second harmonic generation images.

Liu W, Raben N, Ralston E
Journal of biomedical optics.
2013 Feb;
doi: 10.1117/1.JBO.18.2.026005
PMID: 23377006

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Last Updated: May 2020