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Program Director/Principal Investigator (Last, First, Middle): BIOGRAPHICAL SKETCH Provide the following information for the Senior/key personnel and other significant contributors in the order listed on Form Page 2. Follow this format for each person. DO NOT EXCEED FOUR PAGES. NAME POSITION TITLE G. William Wong Associate Professor eRA COMMONS USER NAME (credential, e.g., agency login) gwong9 EDUCATION/TRAINING (Begin with baccalaureate or other initial professional education, such as nursing, include postdoctoral training and residency training if applicable.) DEGREE INSTITUTION AND LOCATION MM/YY FIELD OF STUDY (if applicable) BS Washington State University Summa Cum Laude 1990-94 Biology Harvard University PhD 1994-2000 Immunology Whitehead Institute, M.I.T. Postdoctoral fellow 2001-2007 Biochemistry, Cell Biology, and Physiology A. Personal Statement G. William Wong is currently an Associate Professor in the Department of Physiology and Center for Metabolism and Obesity Research at The Johns Hopkins University School of Medicine. Dr. Wong received his Ph.D. degree from Harvard University, working on innate immunity, followed by post-doctoral training at the Whitehead Institute at M.I.T. In 2008, he joined the faculty at Johns Hopkins University. Current efforts in the laboratory centered on elucidating the physiological functions and mechanisms of action of a novel family of adipose-derived hormones his lab has recently identified. A combination of molecular, cellular, and in vivo (transgenic and knockout) approaches are being used in the lab to address how these secreted hormones mediate inter-tissue crosstalk to control integrated physiology and energy homeostasis. B. Positions and Honors Professional Experience 1990-1994 Undergraduate Research Associate, Department of Genetics and Cell Biology, Washington State University 1994-2000 Ph.D. Student, Division of Medical Science (Program in Immunology), Harvard University 2001-2007 Postdoctoral Fellow, Whitehead Institute for Biomedical Research, MIT 2008-2013 Assistant Professor, Department of Physiology and Center for Metabolism and Obesity Research, Johns Hopkins University School of Medicine 2013Associate Professor, Department of Physiology and Center for Metabolism and Obesity Research, Johns Hopkins University School of Medicine Honors and Awards 2009-2013 American Heart Association Scientist Development Award Grant 2004-2007 NIH National Research Service Award (postdoctoral fellowship) 2000 Pharmacia Allergy Research Award 1992-1993 Howard Hughes Undergraduate Investigator Award C. Selected Peer-reviewed Publications (from a total of 66) PHS 398/2590 (Rev. 06/09) Page Biographical Sketch Format Page Program Director/Principal Investigator (Last, First, Middle): 1. Wong GW, Wang J, Hug C, Tsao T-S, Lodish HF. (2004) A family of Acrp30/adiponectin structural and functional paralogs. Proc Natl Acad Sci U S A. 101:10302-10307. 2. Wong GW, Krawczyk SA, Kitidis C, Gimeno R, Revett T, Lodish HF. (2008) Molecular, biochemical, and functional characterization of C1q/TNF family members: adipose tissue-selective expression patterns, regulation by PPAR-γ agonist, Cys-mediated oligomerizations, combinatorial associations, and metabolic function. Biochemical J. 416:161-77. Corresponding author 3. Wong GW, Krawczyk SA, Kitidis C, Ge G, Hug C, Spooner E, Gimeno R, Lodish HF. (2009) Identification and functional characterization of CTRP9, a novel secreted glycoprotein from adipose tissue, that reduces serum glucose in obese mice and forms heterotrimers with adiponectin. FASEB J. 23:241-58. Corresponding author 4. Peterson JM, Wei Z, Wong GW. (2010) C1q/TNF-related protein-3 (CTRP3), a novel adipokine that regulates hepatic glucose output. J Biol Chem. 285: 39691-39701. 5. Wei Z, Peterson JM, Wong GW. (2011) Metabolic regulation by C1q/TNF-related protein-13 (CTRP13): Activation of AMP-activated protein kinase and suppression of lipid-induced JNK signaling pathway. J Biol Chem. 286: 15652-15665. 6. Gao X, Lowry P, Zhou X, Depry C, Wei Z, Wong GW, Zhang J. (2011) PI3K/Akt signaling requires spatial compartmentalization in plasma membrane microdomains. Proc Natl Acad Sci U S A. 108:14509-14 7. Peterson JM, Aja S, Wei Z, Wong GW. (2012) CTRP1 protein enhances fatty acid oxidation via AMPactivated protein kinase (AMPK) activation and acetyl-CoA carboxylase (ACC) inhibition. J Biol Chem. 287:1576-1587. 8. Wei Z, Peterson JM, Lei X, Cebotaru L, Wolfgang MJ, Baldeviano GC, Wong GW. (2012) C1q/TNF-related protein-12 (CTRP12), a novel adipokine that improves insulin sensitivity and glycemic control in mouse models of obesity and diabetes. J Biol Chem. 287:10301-10315. 9. Seldin MM, Peterson JM, Byerly MS, Wei Z, Wong GW. (2012) Myonectin (CTRP15), a novel myokine that links skeletal muscle to systemic lipid homeostasis. J Biol Chem. 287:11968-11980. 10. Wei Z, Lei X, Seldin MM, Wong GW. (2012) Endopeptidase cleavage generates a functionally distinct isoform of C1q/TNF-related protein-12 (CTRP12) with an altered oligomeric state and signaling specificity. J Biol Chem. 287:35804-35814. 11. Byerly MS, Salayta MA, Kwon K, Swanson R, Peterson JM, Wei Z, Moran TH, Aja S, Blackshaw S, Wong GW. (2013) Estrogen-related Receptor β regulates whole body energy balance and attenuates neuropeptide Y gene expression. Eur. J. Neurosci. 37:1033-1047. 12. Wei Z, Seldin MM, Natarajan N, DjemalDC, Peterson JM, Wong GW. (2013) C1q/TNF-related protein11 (CTRP11), a novel adipose stromal-derived regulator of adipogenesis. J Biol Chem. 288:1021410229. 13. Ellis JM, Wong GW, Wolfgang MJ. (2013) Acyl-CoA Thioesterase 7 regulates neuronal fatty acid metabolism to prevent neurotoxicity. Mol. Cell Biol. 33:1869-1882 14. Byerly MS, Swanson R, Wei Z, Seldin MM, McCulloh PS, Wong GW. (2013) A central role for C1q/TNFrelated protein-13 (CTRP13) in modulating food intake and body weight. PLoS One 8(4): e62862 PHS 398/2590 (Rev. 06/09) Page 2 Continuation Format Page Program Director/Principal Investigator (Last, First, Middle): 15. Byerly MS, Swanson R, Kwon K, Aja S, Moran TH, Wong GW, Blackshaw S. (2013) Identification of hypothalamic neuron-derived neurotrophic factor as a novel factor modulating appetite. Am J Physiol Regul Integr Comp Physiol. 304:R1085-R1095 16. Peterson JM, Seldin MM, Wei Z, Aja S, Wong GW. (2013) CTRP3 attenuates diet-induced hepatic steatosis by regulating triglyceride metabolism. Am J Physiol Gastrointest Liver Physiol. 305:G214224. 17. Peterson JM, Wei Z, Seldin MM, Byerly MS, Aja S, Wong GW. (2013) CTRP9 transgenic mice are protected from diet-induced obesity and metabolic dysfunctions. Am J Physiol Regul Integr Comp Physiol. 305:R522-533. 18. Byerly MS, Swanson R, Wong GW, Blackshaw S. (2013) Stage-specific inhibition of TrkB leads to longlasting and sexually dimorphic effects on body weight and hypothalamic gene expression. PLoS One 8(11):e80781 19. Seldin MM, Lei X, Tan S, Stanson KP, Wei Z, Wong GW. (2013) Skeletal muscle-derived myonectin activates the mTOR pathway to suppress autophagy in liver. J Biol Chem. 288:36073-82 20. Byerly MS, Petersen PS, Ramamurthy S, Seldin MM, Lei X, Provost E, Wei Z, Ronnett GV, Wong GW. (2014) C1q/TNF-related protein-4 (CTRP4) is a unique secreted protein with two tandem C1q domain that functions in the hypothalamus to modulate food intake and body weight. J Biol Chem. 289:40554069 21. Peterson JM, Seldin M,Tan SY, Wong GW. (2014) CTRP2 overexpression improves insulin and lipid tolerance in diet-induced obese mice. PLoS One 9(2):e88535 22. Wei Z, Lei X, Pedersen PS, Aja S, Wong GW. (2014) Targeted deletion of C1q/TNF-related protein 9 (CTRP9) increases food intake, decreases insulin sensitivity, and promotes hepatic steatosis in mice. Am J Physiol Endocrinol Metab. 306:E779-E790 23. Bedont JL, LeGates TA, Slat EA, Byerly MS, Wang H, Hu J, Qian J, Wong GW, , Herzog ED, Hattar S, and Blackshaw S. (2014) Lhx1 controls terminal differentiation and circadian function of the suprachiasmatic nucleus. Cell Rep. 7:1-14 24. Petersen PS, Lei X, Seldin MM, Rodriguez S, Byerly MS, Wolfe A, Whitlock S, Wong GW. (2014) Dynamic and extensive metabolic state-dependent regulation of cytokine expression and circulating levels. Am J Physiol Regul Integr Comp Physiol. 307:R1458-1470 25. Multhaup ML, Seldin MM, Jaffe AE, Lei X, Kirchner H, Mondal P, Li Y, Rodriguez V, Drong A, Hussain M, Lindgren C, McCarthy M, Naslund E, Zierath J, Wong GW, Feinberg AP. (2015) Mouse-human experimental epigenetic analysis unmasks dietary targets and genetic liability for diabetic phenotypes. Cell Metab. 21:138-149 26. Zhou X, Clister TL, Lowry PR, Seldin MM, Wong GW, Zhang J (2015) Dynamic visualization of the mechanistic target of rapamycin complex 1 (mTORC1) activity in living cells. Cell Rep. 10:1-11 27. Lei X, Li Q, Rodriguez S, Tan SY, Seldin MM, McLenithan JC, Jia W, Wong GW. (2015) Thromboxane synthase deficiency improves insulin action and attenuates adipose tissue fibrosis. Am J Physiol Endocrinol Metab. 308: E792-804 28. Wolf RM, Yang ZC, Lei X, Nyandjo M, Tan SY, Wong GW (2016). CTRP3 deficiency reduces liver size and alters IL-6 and TGF-β levels in obese mice. Am J Physiol Endocrinol Metab. 310:E332-E345 PHS 398/2590 (Rev. 06/09) Page 3 Continuation Format Page Program Director/Principal Investigator (Last, First, Middle): 29. Lei X, Rodriguez S, Petersen PS, Seldin MM, Bowman CE, Wolfgang MJ, Wong GW. (2016) Loss of CTRP5 improves insulin sensitivity and hepatic steatosis. Am J Physiol Endocrinol Metab. 310: E1036-E1052 Complete List of Published Work in MyBibliography: http://www.ncbi.nlm.nih.gov/sites/myncbi/guang.wong.1/bibliograpahy/44112468/public/?sort=date&directio n=descending D. Research Support Active 1) Novo Nordisk Diabetes and Obesity Biologics Science Forum Award Title: Functional characterization of the anti-diabetic adipokine, CTRP12 Role on Project: Principal Investigator Goal: This project aims to elucidate the anti-diabetic actions of CTRP12 09/31/14 -09/30/16 2) Human Frontier Science Program 08/01/16 -07/31/19 Title: Optimization of Metabolic Flux in the Hummingbird: From Enzymes to Ecology Role on Project: Co-Investigator Goal: This project aims to use hummingbird as a model system to understand extreme metabolic adaptations PHS 398/2590 (Rev. 06/09) Page 4 Continuation Format Page