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Faculty
Brown, Stuart I. MD
Brody, Barbara MPH
Ferreyra, Henry A. MD
Freeman, William R. MD
Goldbaum, Michael H. MD
Granet, David B. MD
Haw, Weldon, MD
Heichel, Chris MD
Kikkawa, Don O. MD

Korn, Bobby S. MD, PhD
Levi, Leah MD
Medeiros, Felipe MD PhD

Nguyen, Thao MD
Robbins, Shira MD

Savino, Peter J. MD
Schanzlin, David J. MD
Weinreb, Robert N. MD
Zhang, Kang MD, PhD

Research Faculty
Ayyagari, Radha PhD
Bartsch, Dirk- Uwe PhD

Lindsey, James D. PhD
Liu, John H K PhD
Sample, Pamela A. PhD

Silva, Gabriel A. MSc PhD

Zangwill, Linda PhD

Research Scientist

Bowd, Christoper PhD
Cheng, Lingyun MD
Duncan, Robert PhD
Ju, Won-Kyu PhD
Kozak, Igor MD, PhD
Vasireddy, Vidyullatha PhD





 


Won-Kyu Ju, Ph.D.

Assistant Project Scientist,
Glaucoma

http://glaucoma.ucsd.edu/


Won-Kyu Ju is Assistant Project Scientist in the Department of Ophthalmology. He received his M.S. and Ph.D. in Department of Anatomy at Medical College of Catholic University in Korea in 2001, and then completed a 2 year post-doctoral position in the Department of Ophthalmology and Visual Sciences at Washington University in St. Louis studying the mechanisms of cell death and protection in retinal neurodegeneration in retinal ischemia and glaucoma. He worked at the Burnham Institute in San Diego as a senior post-doctoral associate from 2003 and as a staff scientist from 2005 studying the mechanisms of OPA1 mutation-mediated mitochondrial dysfunction in dominant optic atrophy. Dr. Ju published over 30 scientific publications. Dr. Ju is interested in the fundamental issues of whether acute or chronic intraocular pressure (IOP) induces breakdown of mitochondria network, such as mitochondrial fragmentation, and how IOP triggers mitochondrial dysfunction of retinal ganglion cell death in glaucoma. Recently, he has established a specialized pressure model to mimic pressure-induced glaucoma in vitro and has found that hydrostatic pressure induced mitochondrial fission, which may cause cell death, in differentiated retinal ganglion cell (RGC-5). He has also begun investigating mitochondrial dysfunction in mouse glaucoma in vivo model by acute or chronic IOP elevation. This work will be extremely important to determine how mitochondrial dysfunction contributes to progressive RGC degeneration and identify new potential targets for therapeutic intervention in glaucoma.