Principal Investigator
Yoshiaki Tsuji, PhD
Professor
Department of Biological Sciences, Environmental and Molecular Toxicology Program
Phone: 919-513-110
6
Fax: 919-515-7169
e-mail: yoshiaki_tsuji@ncsu.edu
Lab: Rm #2230, #2232, and #2232A, Office: Rm #2203
Ph.D. in Cell Biology, Hiroshima University School of Medicine, Hiroshima, Japan
Postdoctoral Fellow, Stanford University School of Medicine, Palo Alto, California
Lab Members
Masaki Miyazawa, PhD (Postdoctoral fellow, 5. 2011~ 9. 2017) mmiyaza2@ncsu.edu
The goal of my current research is to investigate the molecular interphase between genotoxic drugs and cellular stress response. In particular, my research focuses on intracellular localization and expression of Shc proteins and regulation of antioxidant genes under genotoxic and oxidative stress conditions. p66Shc, one isoform of Shc, appears to be a mitochondrial adaptor protein to control oxidative stress response; however, its roles in cell signaling and mitochondrial homeostasis have been incompletely understood. My work in this project is to clarify the involvement of p66Shc in genotoxic and oxidative stress through characterization of a specific signaling pathway leading to mitochondrial expression of p66Shc and its impact on cellular antioxidant gene expression.
M. Miyazawa and Y. Tsuji
“Evidence for a Novel Antioxidant Function and Isoform-specific Regulation of the Human p66Shc Gene”
Mol. Biol. Cell 25: 2116-2127 (2014)
B.W. Huang, M. Miyazawa, and Y. Tsuji
Distinct Regulatory Mechanisms of the Human Ferritin Gene by Hypoxia and Hypoxia Mimetic Cobalt Chloride at the Transcriptional and Post-transcriptional Levels
Cell. Signal., 26: 2702-2709 (2014)
A.R. Bogdan, M. Miyazawa, K. Hashimoto, Y. Tsuji
“Regulators of Iron Homeostasis: new players in metabolism, cell death, and disease”
Trends Biochem. Sci., 41: 274-286 (2016)
B.R. Wilson, A.R. Bogdan, M. Miyazawa, K. Hashimoto, Y. Tsuji
“Siderophores in Iron Metabolism: From Mechanism to Therapy Potential”
Trends Mol. Med., 22: 1077-1090 (2016)
Kazunori Hashimoto, PhD (Postdoctoral Fellow, 4. 2012~ 11. 2017) khashim@ncsu.edu
My research goal is to investigate how neurological diseases affect the normal cellular responses to genotoxic and oxidative stress including arsenic. Arsenic is naturally found throughout the earth’s crust and is widely distributed throughout the environment. Long-term exposure to arsenic from water and food can cause skin lesions and cancer, and has also been associated with many neurological diseases. Currently, my work elucidates protective cellular response against arsenic, particularly through homeodomain interacting protein kinase 2 (HIPK2) activation. HIPK2 is a serine/threonine kinase that phosphorylates CREB and ATF1 transcription factors at novel sites. However, the roles of the novel phosphorylation sites remain elusive. My research focuses on how HIPK2 regulates a cellular defense system under genotoxic and oxidative stress through new phosphorylation of CREB and ATF-1.
A.R. Bogdan, M. Miyazawa, K. Hashimoto, Y. Tsuji
“Regulators of Iron Homeostasis: new players in metabolism, cell death, and disease”
Trends Biochem. Sci., 41: 274-286 (2016)
K. Hashimoto, AN. Simmons, R. Kajino-Sakamoto, Y. Tsuji, J. Ninomiya-Tsuji.
TAK1 regulates the Nrf2 antioxidant system through modulating p62/ SQSTM1.
Antioxid Redox Signal., 25: 953-964 (2016)
B.R. Wilson, A.R. Bogdan, M. Miyazawa, K. Hashimoto, Y. Tsuji
“Siderophores in Iron Metabolism: From Mechanism to Therapy Potential”
Trends Mol. Med., 22: 1077-1090 (2016)
K. Hashimoto, Y. Tsuji
“Arsenic-induced Activation of the Homeodomain Interacting Protein Kinase 2 (HIPK2) to cAMP-Response Element Binding Protein (CREB) Axis”
J. Mol. Biol., in press (2017)
Alexander Bogdan (PhD in Toxicology, 1. 2011~11. 2016 ) arbogdan@ncsu.edu
Iron is an essential micronutrient, serving as a critical co-factor in cellular processes such as DNA replication and ATP generation. However, intracellular iron can undergo redox chemistry, catalyzing the formation of damaging reactive oxygen species. To ensure that cells maintain an adequate but nontoxic amount of iron, the expression of genes involved in iron metabolism (IM) is tightly regulated both transcriptionally and post-transcriptionally, via mRNA-binding Iron Regulatory Proteins. Recently, microRNAs are recognized as central mediators in the post-transcriptional regulation of genes, but the both the role of microRNAs in IM and the interplay of microRNAs with other post-transcriptional regulation systems are unclear. My research focuses on how microRNAs regulate expression of IM genes, and how microRNAs act in concert with or in opposition to Iron Regulatory Proteins in managing expression of IM genes.
A.R. Bogdan, M. Miyazawa, K. Hashimoto, Y. Tsuji
“Regulators of Iron Homeostasis: new players in metabolism, cell death, and disease”
Trends Biochem. Sci., 41: 274-286 (2016)
B.R. Wilson*, A.R. Bogdan*, M. Miyazawa, K. Hashimoto, Y. Tsuji
“Siderophores in Iron Metabolism: From Mechanism to Therapy Potential”
Trends Mol. Med., 22: 1077-1090 (2016) *co-first authors
Briana Roulhac-Wilson (MS in Physiology, 6. 2014~6. 2016 ) bdroulha@ncsu.edu
Mechanisms that limit cellular damage as a result of environmental insults are necessary to prevent common human diseases such as cancer and neurodegeneration. These mechanisms involve crucial cell signaling pathways and oxidative stress responses. The cAMP-response element binding (CREB) protein is an important transcription factor involved in the well-characterized PKA pathway. However, CREB’s function in cell signaling pathways that respond to such insults remains poorly understood. Previously this lab found a novel CREB phosphorylation site. My research focuses on further characterizing this new phosphorylation site, as well as elucidating its place in less well-characterized pathways. Regulation and expression of cellular oxidative stress genes also have an important role in maintaining cellular viability. Ferritin H, a component of the iron chelator protein ferritin, plays an integral role in preventing oxidative stress in the cell. I am interested in the mechanisms by which the ferritin H transcript may be stabilized following stressful stimuli.
B.R. Wilson*, A.R. Bogdan*, M. Miyazawa, K. Hashimoto, Y. Tsuji
“Siderophores in Iron Metabolism: From Mechanism to Therapy Potential”
Trends Mol. Med., 22: 1077-1090 (2016) *co-first authors
Former Lab Members and Research
Graduate Students
Sree Ranjani Ramani 12. 2003 – 6. 2005, MS
Kiros Hailemariam 3. 2002 – 4. 2007, PhD
• K. Hailemariam, K. Iwasaki, B-W. Huang, K. Sakamoto, and Y. Tsuji
“Transcriptional regulation of ferritin and antioxidant genes by HIPK2 in genotoxic stress”
J. Cell Sci., 123: 3863-3871 (2010)
• K. Sakamoto, B-W. Huang, K. Iwasaki, K. Hailemariam, J. Ninomiya-Tsuji and Y. Tsuji
“Regulation of Genotoxic Stress Response by Homeodomain-interacting Protein Kinase 2 through Phosphorylation of Cyclic AMP Response Element-binding Protein at Serine 271”
Mol. Biol. Cell 21: 2966-2974 (2010)
• K. Iwasaki, K. Hailemariam and Y. Tsuji.
“Protein Inhibitor of Activated STAT3 (PIAS3) Interacts with Activating Transcription Factor 1 (ATF1) and Regulates an Antioxidant Responsive Element of the Human Ferritin H Gene”
J. Biol. Chem., 282: 22335-22343 (2007)
• K. Iwasaki, E. L. MacKenzie, K. Hailemariam, K. Sakamoto and Y. Tsuji.
“Hemin-mediated Regulation of an Antioxidant Responsive Element of the Human Ferritin H Gene and Role of Ref-1 during Erythroid Differentiation of K562 Cells”
Mol. Cell. Biol., 26: 2845-2856 (2006).
Elizabeth MacKenzie 3. 2003 – 2. 2007, PhD
• E.L. MacKenzie, P. D. Ray and Y. Tsuji.
“Role and Regulation of Ferritin H in Rotenone-mediated Mitochodrial Oxidative Stress”
Free Radic. Biol. Med., 44: 1762-1771 (2008)
• E.L. MacKenzie and Y. Tsuji.
“Elevated Intracellular Calcium Increases Ferritin H Expression through an NFAT-independent Posttranscriptional Mechanism Involving mRNA Stabilization”,
Biochem. J., 411: 107-113 (2008)
• E.L. MacKenzie, K. Iwasaki and Y. Tsuji
“Intracellular Iron Transport and Storage: From Molecular Mechanisms to Health Implications”
Antioxid. Redox Signaling, 10: 997-1030 (2008)
• K. Iwasaki*, E. L. MacKenzie*, K. Hailemariam, K. Sakamoto and Y. Tsuji.
“Hemin-mediated Regulation of an Antioxidant Responsive Element of the Human Ferritin H Gene and Role of Ref-1 during Erythroid Differentiation of K562 Cells”
Mol. Cell. Biol., 26: 2845-2856 (2006).
• E. L. MacKenzie “Reactive Oxygen/reactive Metabolites and Toxicity”
Chapter 20 In Molecular and Biochemical Toxicology, 4th Edition, R.C. Smart and E. Hodgson, Wiley Interscience, 389-411 (2008)
Kensuke Sakamoto 4. 2005 – 2. 2009, PhD
• K. Iwasaki, P.D. Ray, B.W Huang. K. Sakamoto, T. Kobayashi, Y Tsuji,
“Role of AMP-activated Protein Kinase in Ferritin H Gene Expression by Resveratrol in Human T Cells”
Biochemistry 52: 5075-5083 (2013)
• K. Hailemariam, K. Iwasaki, B-W. Huang, K. Sakamoto, and Y. Tsuji
“Transcriptional regulation of ferritin and antioxidant genes by HIPK2 in genotoxic stress”
J. Cell Sci., 123: 3863-3871 (2010)
• K. Sakamoto, B-W. Huang, K. Iwasaki, K. Hailemariam, J. Ninomiya-Tsuji and Y. Tsuji
“Regulation of Genotoxic Stress Response by Homeodomain-interacting Protein Kinase 2 through Phosphorylation of Cyclic AMP Response Element-binding Protein at Serine 271”
Mol. Biol. Cell 21: 2966-2974 (2010)
• K. Sakamoto, K. Iwasaki, H. Sugiyama and Y. Tsuji
“Role of the Tumor Suppressor PTEN in Antioxidant Responsive Element-mediated Transcription and Associated Histone Modifications”
Mol. Biol. Cell 20: 1606-1617 (2009)
• K. Iwasaki, E. L. MacKenzie, K. Hailemariam, K. Sakamoto and Y. Tsuji.
“Hemin-mediated Regulation of an Antioxidant Responsive Element of the Human Ferritin H Gene and Role of Ref-1 during Erythroid Differentiation of K562 Cells”
Mol. Cell. Biol., 26: 2845-2856 (2006).
Paul Ray 12. 2006 – 6. 2012, PhD
• P.D Ray, B.W Huang, and Y. Tsuji
“Coordinated Regulation of Nrf2 and Histone H3 Serine 10 Phosphorylation in Arsenite-activated Transcription of the Human Heme Oxygenase-1 Gene”
BBA – Gene Regulatory Mechanisms, 1849: 1277-1288 (2015)
• K. Iwasaki, P.D. Ray, B.W Huang, K. Sakamoto, T. Kobayashi, Y Tsuji,
“Role of AMP-activated Protein Kinase in Ferritin H Gene Expression by Resveratrol in Human T Cells”.
Biochemistry 52: 5075-5083 (2013)
• B.W Huang, P.D. Ray, K. Iwasaki, and Y. Tsuji
“Transcriptional Regulation of the Human Ferritin Gene by Coordinated Regulation of Nrf2 and Protein Arginine Methyltransferases PRMT1 and PRMT4”
FASEB J., 27: 3763-3774 (2013)
• P.D Ray, B.W Huang, and Y. Tsuji.
“Reactive Oxygen Species (ROS) Homeostasis and Redox Regulation in Cellular Signaling”
Cell. Signal., 24: 981-990 (2012)
• E.L. MacKenzie, P. D. Ray and Y. Tsuji.
“Role and Regulation of Ferritin H in Rotenone-mediated Mitochodrial Oxidative Stress”
Free Radic. Biol. Med., 44: 1762-1771 (2008)
Bo-Wen Huang 5. 2007 – 7.2012, PhD
• P.D Ray, B.W Huang, and Y. Tsuji
“Coordinated Regulation of Nrf2 and Histone H3 Serine 10 Phosphorylation in Arsenite-activated Transcription of the Human Heme Oxygenase-1 Gene”
BBA – Gene Regulatory Mechanisms, 1849: 1277-1288 (2015)
• B.W Huang, M. Miyazawa, and Y. Tsuji
Distinct Regulatory Mechanisms of the Human Ferritin Gene by Hypoxia and Hypoxia Mimetic Cobalt Chloride at the Transcriptional and Post-transcriptional Levels
Cell. Signal., 26: 2702-2709 (2014)
• B.W Huang, P.D. Ray, K. Iwasaki, and Y. Tsuji
“Transcriptional Regulation of the Human Ferritin Gene by Coordinated Regulation of Nrf2 and Protein Arginine Methyltransferases PRMT1 and PRMT4”
FASEB J., 27: 3763-3774 (2013)
• K. Iwasaki, P.D. Ray, B.W Huang, K. Sakamoto, T. Kobayashi, Y Tsuji,
“Role of AMP-activated Protein Kinase in Ferritin H Gene Expression by Resveratrol in Human T Cells”.
Biochemistry 52: 5075-5083 (2013)
• P.D Ray, B.W Huang, and Y. Tsuji.
“Reactive Oxygen Species (ROS) Homeostasis and Redox Regulation in Cellular Signaling”
Cell. Signal., 24: 981-990 (2012)
• K. Hailemariam, K. Iwasaki, B-W. Huang, K. Sakamoto, and Y. Tsuji
“Transcriptional regulation of ferritin and antioxidant genes by HIPK2 in genotoxic stress”
J. Cell Sci., 123: 3863-3871 (2010)
• K. Sakamoto, B-W. Huang, K. Iwasaki, K. Hailemariam, J. Ninomiya-Tsuji and Y. Tsuji
“Regulation of Genotoxic Stress Response by Homeodomain-interacting Protein Kinase 2 through Phosphorylation of Cyclic AMP Response Element-binding Protein at Serine 271”
Mol. Biol. Cell 21: 2966-2974 (2010)
Postdoctoral Fellows
Kenta Iwasaki, PhD (11. 2003 – 3. 2008)
• K. Iwasaki, P.D. Ray, B.W Huang. K. Sakamoto, T. Kobayashi, Y Tsuji,
“Role of AMP-activated Protein Kinase in Ferritin H Gene Expression by Resveratrol in Human T Cells”.
Biochemistry 52: 5075-5083 (2013)
• B.W Huang, P.D. Ray, K. Iwasaki, and Y. Tsuji
“Transcriptional Regulation of the Human Ferritin Gene by Coordinated Regulation of Nrf2 and Protein Arginine Methyltransferases PRMT1 and PRMT4”
FASEB J., 27: 3763-3774 (2013)
• K. Hailemariam, K. Iwasaki, B-W. Huang, K. Sakamoto, and Y. Tsuji
“Transcriptional regulation of ferritin and antioxidant genes by HIPK2 in genotoxic stress”
J. Cell Sci., 123: 3863-3871 (2010)
• K. Sakamoto, B-W. Huang, K. Iwasaki, K. Hailemariam, J. Ninomiya-Tsuji and Y. Tsuji
“Regulation of Genotoxic Stress Response by Homeodomain-interacting Protein Kinase 2 through Phosphorylation of Cyclic AMP Response Element-binding Protein at Serine 271”
Mol. Biol. Cell 21: 2966-2974 (2010)
• E.L. MacKenzie, K. Iwasaki and Y. Tsuji
“Intracellular Iron Transport and Storage: From Molecular Mechanisms to Health Implications”
Antioxid. Redox Signaling, 10: 997-1030 (2008)
• K. Iwasaki, K. Hailemariam and Y. Tsuji.
“Protein Inhibitor of Activated STAT3 (PIAS3) Interacts with Activating Transcription Factor 1 (ATF1) and Regulates an Antioxidant Responsive Element of the Human Ferritin H Gene”
J. Biol. Chem., 282: 22335-22343 (2007)
• K. Iwasaki, E. L. MacKenzie, K. Hailemariam, K. Sakamoto and Y. Tsuji.
“Hemin-mediated Regulation of an Antioxidant Responsive Element of the Human Ferritin H Gene and Role of Ref-1 during Erythroid Differentiation of K562 Cells”
Mol. Cell. Biol., 26: 2845-2856 (2006).