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Diabetes 54:3175-3181, 2005
© 2005 by the American Diabetes Association, Inc.

Impaired Generation of Reactive Oxygen Species in Leprechaunism Through Downregulation of Nox4

Hye Sun Park1, Dong Kyu Jin2, Sang Min Shin2, Mi Kyung Jang2, Nicholas Longo3, Ji Won Park1, Duk Soo Bae4, and Yun Soo Bae1

1 Division of Molecular Life Sciences, Center for Cell Signaling Research, Ewha Womans University, Seoul, Korea
2 Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Ilwon-Dong, Kangnam-Gu, Seoul, Korea;
3 Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, Utah
4 Department of Obstetrics and Gynecology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Ilwon-Dong, Kangnam-Gu, Seoul, Korea

Leprechaunism features a clinical constellation characterized by extreme insulin resistance, growth retardation, and several distinct developmental abnormalities. One puzzling observation about leprechaunism is that mutations in the insulin receptor gene frequently associated with this syndrome cannot account for the aberrant responses of cultured cells to other growth factors. Here we report that the generation of reactive oxygen species (ROS) is impaired in cells from leprechaunism patients, thus shedding new light on this issue. Stimulation of patients’ skin fibroblast cells with platelet-derived growth factor (PDGF) resulted in a lower-level tyrosine phosphorylation of cytosolic proteins compared with that seen in normal cells. In addition, consistent with the hypothesis that ROS mediate the level of tyrosine phosphorylation of cytosolic proteins through inactivation of protein tyrosine phosphatases (PTPases), patient fibroblast cells showed a significantly higher phosphatase activity than normal cells. We further showed that the lower-level tyrosine phosphorylation in response to growth factors results from the downregulation of an NADPH oxidase, Nox4, which in turn results in the reduction of ROS generation. Ectopic expression of Nox4 in the patient fibroblast cells consistently restored PDGF-induced ROS production and regulation of PTPase activities. Taken together, these data provide insight into the mechanisms through which growth retardation is associated with leprechaunism syndrome.


Address correspondence and reprint requests to Yun Soo Bae, PhD, Center for Cell Signaling Research, Division of Molecular Life Sciences, Ewha Womans University, 11-1 Daehyun-Dong, Seodaemoon-Gu, Seoul 120-750, Korea. E-mail: baeys{at}ewha.ac.kr. Or Dong Kyu Jin, Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Ilwon-Dong, Kangnam-Gu, Seoul, Korea. E-mail: jindk{at}smc.samsung.co.kr

Abbreviations: DCF-DA, 2',7' dichlorofluorescein diacetate; DMEM, Dulbecco’s modified Eagle’s medium; DTT, dithiothreitol; EGF, epidermal growth factor; NOXO1, Nox organizing protein 1; PDGF, platelet-derived growth factor; PTPase, protein tyrosine phosphatase; RMS, Rabson-Mendenhall syndrome; ROS, reactive oxygen species


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