Personal History:University of Virginia, Department of Biology: BA with Highest Distinction
I worked with MS Grace studying infrared reception in Boid snakes. Our work focused on the behavioral contribution of infrared sensory systems on prey targeting.
University of Washington, Department of Biology: PhD
I worked with AOD Willows, a pioneer in describing the neural networks that underlie behavior, and the former Director of the Friday Harbor Laboratories. Using the model T. diomedea, we described how a CNS controls and coordinates the beating of epithelial cilia to produce the animals normal crawling behavior. We found that neurotransmitters and peptides were being secreted by neurites in the foot inhibiting Ca2+ activated Cl- currents. These currents are key in regulating cilia beating frequency. Our work demonstrated how a nervous system can finely control non-excitable cells and coordinate cilia beating across an entire epithelium, a function critical in the human lung and brain.
The Johns Hopkins University School of Medicine, Department of Physiology: Post Doctoral Research Fellow
I worked with the Director of Physiology, WB Guggino, studying epithelial transporters and ion channels. Dr. Guggino has made many of the seminal discoveries that shape our understanding of anion conductances and transport in epithelial cells, and our work focused on understanding transporters and ion channels in human disease: CFTR and cystic fibrosis; Polycytsin 1 and 2 in polycystic kidney disease, and ABCG2 in gout and hyperuricemia.
Research Interests:My work has come to focus on the complicated workings of the human kidney and understanding how genetic mutations lead to disease, describing the physiological mechanism, and finding possible therapies.
ABCG2, Hyperuricemia, and gout
Urate (uric acid) handling and secretion in humans and the great apes is unique among mammals; we have lost the function of the urate oxidase (uricase) enzyme, the enzyme responsible for metabolizing urate into allantoin. The loss of uricase appears to be adaptive in humans, however it puts humans at risk for retaining too much urate (hyperuricemia), which can lead to gout, kidney disease, hypertension, metabolic disorders and cardiovascular disease. Yet, until recently the transporters responsible for urate secretion and absorption remained mostly unknown.
Recently, we discovered that ABCG2 is a novel urate transporter, perhaps the most important secretion mechanism for uric acid in humans, and identified a loss of function mutation that causes hyperuricemia and gout. Importantly the mutation is common, carried by almost a billion people, putting them at increased risk for hyperuricemia, gout, and possibly hypertension and other metabolic diseases. Most recently, we have gained an understanding of how this mutation causes dysfunction in ABCG2 and have used this new understanding to find small molecules that can correct the defect, a proof of principal that new small molecule therapy may be possible for hyperuricemia and gout.
ROMK and hypertension
I am working with PA Welling to better our understanding of how the function of the important renal K+ channel, ROMK, is regulated in the renal tubule. ROMK is known to be regulated by the WNK kinases, kinases that can carry mutations that cause familial hyperkalemic hypertension. What is not known is the mechanistic connection between the WNK kinases and the surface expression of ROMK, but recent work by Dr. Welling has shown that the WNKs may specifically regulate ROMK endocytosis and therefore its degradation. All of the relevant players are not yet known and our work hopes to indentify the remaining parts of the regulatory pathway, an effort bent at finding new and better ways to treat hypertension
Lab Techniques and Equipment:Our work uses many different tools, all focused on understanding the physiology of the human kidney. We use genetic studies to find disease causing mutations and test the mutant protein’s function with radioactive transport assays, patch clamp studies, two electrode voltage clamp, live cell imaging, and FRET. And finally we use mouse models to gain a better understanding of how mutant proteins fit into the whole animal physiology.
1. Woodward, O.M.†, Tukaye, D.N., Cui, J., Greenwell P., Constantoulakis, L.M., Parker B.S., Rao, A., Kottgen, M., Maloney P.C., and Guggino, W.B. (2013) Gout causing Q141K mutation in ABCG2 leads to instability of the nucleotide binding domain and can be corrected with small molecules. Proc Natl Acad Sci USA. 110(13):5223-5228 (†Corresponding Author)
2. Anna Köttgen, Eva Albrecht, Alexander Teumer, Veronique Vitart, Jan Krumsiek, Claudia Hundertmark, Giorgio Pistis, Daniela Ruggiero, Conall M O’Seaghdha, Toomas Haller, Qiong Yang, Toshiko Tanaka, Andrew D Johnson, Zoltán Kutalik, Albert V Smith, Julia Shi, Maksim Struchalin, Rita PS Middelberg, Morris J Brown, Angelo L Gaffo, Nicola Pirastu, Guo Li, Caroline Hayward, Tatijana Zemunik, Jennifer Huffman, Loic Yengo, Jing Hua Zhao, Ayse Demirkan, Mary F Feitosa, Xuan Liu, Giovanni Malerba, Lorna M Lopez, Pim van der Harst, Xinzhong Li, Marcus E Kleber, Andrew A Hicks, Ilja M Nolte, Asa Johansson, Federico Murgia, Sarah H Wild, Stephan JL Bakker, John F Peden, Abbas Dehghan, Maristella Steri, Albert Tenesa, Vasiliki Lagou, Perttu Salo, Massimo Mangino, Lynda M Rose, Terho Lehtimäki, Owen M. Woodward, Yukinori Okada, et al. (2013) Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics. 45(2): 145-54.
3. Cebotaru L, Woodward O.M., Cebotaru V, Guggino WB. (2013) Transcomplementation by a truncation mutant of CFTR enhances Delta F508 processing through a biomolecular interaction. J Biol Chem. Mar 5. [Epub ahead of print]
4. Okada Y, Sim X, Go MJ, Wu JY, Gu D, Takeuchi F, Takahashi A, Maeda S, Tsunoda T, Chen P, Lim SC, Wong TY, Liu J, Young TL, Aung T, Seielstad M, Teo YY, Kim YJ, Lee JY, Han BG, Kang D, Chen CH, Tsai FJ, Chang LC, Fann SJ, Mei H, Rao DC, Hixson JE, Chen S, Katsuya T, Isono M, Ogihara T, Chambers JC, Zhang W, Kooner JS; KidneyGen Consortium; CKDGen Consortium, Albrecht E; GUGC consortium, Yamamoto K, Kubo M, Nakamura Y, Kamatani N, Kato N, He J, Chen YT, Cho YS, Tai ES, Tanaka T. (2012) Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Nature Genetics. 44(8): 904-9 (Member of the GUGC consortium).
5. Hoque, K.M., Chakrabarti, S., Ali, S.I., and Woodward, O.M. (2012) New advances in the pathophysiology of intestinal ion transport and barrier function in diarrhea and the impact of therapy. Expert Rev Anti Infect Ther. Jun; 10(6):687-99.
6. Woodward, O.M. and Guggino, W.B. (2012) Anion channels of the human kidney, in Seldin and Geibesh’s The Kidney: Physiology and Pathophysiology. Fifth edition. Academic Press, New York.
7. Woodward, O.M., Kottgen, A., and Kottgen, M. (2011) ABCG transporters and disease. FEBS J. Sep; 278(18): 3215-25.
8. Tin A*, Woodward OM*, Kao WH, Liu CT, Lu X, Nalls AM, Shriner D, Semmo M, Akylbekova EL, Wyatt SB, Hwang SJ, Yang Q, Zonderman AB, Adeyemo A, Palmer C, Meng Y, Reilly MP, Shlipak MG, Siscovick DS, Evans MK, Rotimi CN, Flessner MF, Köttgen M, Cupples LA, Fox CS, and Köttgen A (2011) Genome-wide Association Study for Serum Urate Concentrations and Gout among African Americans Identifies Genomic Risk Loci and a Novel URAT1 Loss-of-Function Allele. Hum Mol Genet. Oct 15;20(20): 4056-68 (*equal contribution) PMCID: PMC3177647
9. Liang, L., Woodward, O.M., Chen, Z., Cotter, R., and Guggino, W.B. (2011) A novel role in protein tyrosine kinase 2 in mediating chloride secretion in human airway epithelial cells. PLoS ONE. 6(7): e21991. PMCID: PMC3135607
10. Woodward, O.M., Li, Y.,Yu, S., Greenwell, P., Wodarczyk, C., Boletta, A., Guggino, W.B., and Qian, F. (2010) Identification of a Polycystin-1 cleavage product, P100, that regulates store operated Ca2+ entry through interactions with STIM1. PLoS ONE. 5(8): e12305. PMCID: PMC2925899
11. Kwon, Y., Kim, S.H., Ronderos, D.S., Lee, Y., Akitake, B., Woodward, O.M., Guggino, W.B., Smith, D.P., and Montell, C. (2010) Drosophila TRPA1 channel is required to avoid the naturally occurring insect repellent citronellal. Current Biology. Volume 20 issue 18, 1672-1678, 25 August 2010. PMCID: PMC2946437
12. Kim, S.H., Lee, Y., Akitake, B., Woodward, O.M., Guggino, W.B., and Montell, C. (2010) Drosophila TRPA1 channel mediates chemical avoidance in gustatory receptor neurons. Proc Natl Acad Sci USA. 107(18):8440-5. PMCID: PMC2889570
13. Woodward, O.M., Kottgen, A., Coresh, J., Boerwinkle, E., Guggino, W.B., and Kottgen, M. (2009) Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout. Proc Natl Acad Sci USA. 106(25):10338-42. PMCID: PMC2700910
14. Hoque KM, Woodward OM, van Rossum DB, Zachos NC, Chen L, Leung GP, Guggino WB, Guggino SE, and Tse, CM. (2010). Epac1 mediates protein kinase A-independent mechanism of forskolin-activated intestinal chloride secretion. J Gen Physiol. 135(1):43-58. PMCID: PMC2806414
15. Li, Y., Santoso, N.G., Yu, S., Woodward, O.M., Qian, F., Guggino, W.B. (2009) Polycystin-1 interacts with IP3R to modulate intracellular Ca2+ signaling, with implications for polycystic kidney disease. J Biol Chem. 284(52):36431-41. PMCID: PMC2794759
16. Woodward, O.M.† and Willows, A.O. (2006). Dopamine modulation of Ca2+ dependent Cl- current regulates ciliary beat frequency controlling locomotion in Tritonia diomedea. J Exp Biol. 209, 2749-2764. (†Corresponding Author)
17. Woodward, O.M.† and Willows, A.O. (2006). Nervous control of ciliary beating by Cl-, Ca2+ and calmodulin in Tritonia diomedea. J Exp Biol. 209, 2765-2773. (†Corresponding Author)
18. Wyeth, R.C., Woodward, O.M., and Willows, A. O. (2006). Orientation and navigation relative to water flow, prey, conspecifics, and predators by the nudibranch mollusc Tritonia diomedea. Biol Bull. 210, 97-108.
19. Grace, M.S., Woodward, O.M., Church, D.R., and Calisch, G. (2001). Prey targeting by the infrared-imaging snake Python molurus: effects of experimental and congenital visual deprivation. Behav Brain Res. 119, 23-31.
20. Grace, M.S. and Woodward, O.M. (2001). Altered visual experience and acute visual deprivation affect predatory targeting by infrared-imaging Boid snakes. Brain Res. 919, 250-258.
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