Ningning Zhao, PhD

Assistant Professor, Department of Nutritional Sciences


  • Postdoctoral Researcher, Cell Biology, Oregon Health & Science University
  • Ph.D., Nutritional Sciences (Molecular Nutrition), University of Florida
  • M.Ed., Sports Science (Sports Nutrition and Exercise Biochemistry), Beijing Sport University
  • B.S., Sports Science (Exercise Biochemistry), Beijing Sport University


Summary of Current Research

The work in our Lab is focused on advancing molecular mechanisms for the function and regulation of plasma membrane metal transporters. These transporters play fundamental roles in regulating cellular metabolism and cellular function. Mutations and malfunctioning of these transporters are directly pertinent to the initiation and the progression of an increasing number of human diseases, including iron deficiency, hemochromatosis, cancer, and childhood on-set neurodegeneration. We identify and characterize the genes and factors that are involved in determining the structure and function of these metal transporters. We also examine the intracellular trafficking and degradation of these proteins.

In our research, we combine cell-line and mouse models, and employ a variety of biochemical and molecular biology techniques. We also utilize the cutting-edge genome engineering technologies, including Adeno-Associated Virus-mediated genomic modification and CRISPR/Cas9-mediated genome editing. We hope that our research will advance the understanding of disease mechanisms, identify therapeutic target genes, and improve the life quality of patients.

Join Our Lab

Welcome! We are seeking energetic and highly motivated researchers, including graduate students and postdoctoral researchers. If interested, please send an inquiry about openings to and attach your CV and personal statement (please highlight your academic background and research experience in the statement).

Students should apply to a graduate program at the UA. Graduate students already enrolled at the UA and are interested in rotating in the lab can contact Ningning directly. A list of three references is required for postdoctoral applicants.

Selected Publications (*corresponding author)

  • Felber D.M., Wu Y., Zhao N.*, Regulation of metal transporter, ZIP14 and ZnT10, by manganese intake in mice. Nutrients, 2019; 11(9): 2099. PMID: 31487869.
  • Scheiber I.F., Alarcon N.O., Zhao N.*, Manganese uptake by A549 cells is mediated by both ZIP8 and ZIP14. Nutrients, 2019; 11(7): 1473. PMID: 31261654.
  • Scheiber I.F., Wu Y., Morgan S.E., Zhao N.*, The intestinal metal transporter ZIP14 maintains systemic manganese homeostasis. The Journal of Biological Chemistry, 2019; 294(23): 9147-9160. PMID: 31028174.
  • Zhao N.*, Zhang A.S., Wortham A.M., Jue S., Knutson M.D., and Enns C.A., The Tumor Suppressor, P53, Decreases the Metal Transporter, ZIP14. Nutrients, 2017; 9 (12): 1335. PMID: 29292794.
  • Wahedi M., Wortham A.M., Kleven M.D., Zhao N., Jue S., Enns C.A., Zhang A.S., Matriptase-2 Suppresses Hepcidin Expression by Cleaving Multiple Components of the Hepcidin Induction Pathway. The Journal of Biological Chemistry, 2017; 292(44):18354-18371. PMID: 28924039.
  • Zhao N., Maxson J. E., Zhang R. H., Wahedi M., Enns C. A., and Zhang A. S., Neogenin Facilitates the Induction of Hepcidin Expression by Hemojuvelin in the Liver. The Journal of Biological Chemistry2016; 291(23): 12322-12335. PMID: 27072365.
  • Tuschl K., Meyer E., Valdivia L.E., Zhao N., Dadswell, C., Abdul-Sada, A., Hung, C. Y., Simpson, M. A., Chong, W. K., Jacques, T. S., Woltjer, R. L., Eaton, S., Gregory, A., Sanford, L., Kara, E., Houlden, H., Cuno, S. M., Prokisch, H., Valletta, L., Tiranti, V., Younis, R., Maher, E. R., Spencer, J., Straatman-Iwanowska, A., Gissen, P., Selim, L. A., Pintos-Morell, G., Coroleu-Lletget, W., Mohammad, S. S., Yoganathan, S., Dale, R. C., Thomas, M., Rihel, J., Bodamer, O. A., Enns, C. A., Hayflick, S. J., Clayton, P. T., Mills, P. B., Kurian, M. A., Wilson, S. W., Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia. Nature Communications2016; 7:11601. PMID: 27231142.
  • Zhao N., Nizzi C.P., Anderson S.A., Wang J., Ueno A., Tsukamoto H., Eisenstein R.S., Enns C.A. and Zhang A.S., Low intracellular iron increases the stability of matriptase-2. The Journal of Biological Chemistry2015; 290(7): 4432-4446. PMID: 25550162.
  • Zhao N., Zhang A.S., Worthen C., Knutson M.D., and Enns C.A., An iron-regulated and glycosylation-dependent proteasomal degradation pathway for the plasma membrane metal transporter ZIP14. Proceedings of the National Academy of Sciences of the United States of America2014; 11(25): 9175-9180. PMID: 24927598.
  • Zhao N., Zhang A.S. and Enns C.A., Iron regulation by hepcidin. Journal of Clinical Investigation2013; 123 (6): 2337-2343. PMID: 23722909.
  • Zhao N. and Enns C.A., N-linked glycosylation is required for transferrin-induced stabilization of transferrin receptor 2, but not for transferrin binding or trafficking to the cell surface. Biochemistry2013; 52: 3310-3319. PMID: 23556518.
  • Zhao N. and Enns C.A., Iron transport machinery of human cells: players and their interactions. Current Topics in Membranes2012; 69: 67-93. PMID: 23046647.
  • Pinilla-Tenas J.J., Sparkman B.K., Shawki A., Illing A.C., Mitchell C.J., Zhao N., Liuzzi J.P., Cousins R.J., Knutson M.D., Mackenzie B., Zip14 is a complex broad-scope metal-ion transporter whose functional properties support roles in the cellular uptake of zinc and nontransferrin-bound iron. American Journal of Physiology-Cell Physiology2011; 301(4): C862-71. PMID: 21653899.
  • Zhao N., Gao J., Enns C.A., Knutson M.D., ZRT/IRT-like protein 14 (ZIP14) promotes the cellular assimilation of iron from transferrin. The Journal of Biological Chemistry2010; 285(42): 32141-32150. PMID: 20682781.
  • Gao J., Zhao N., Knutson M.D., Enns C.A., The hereditary hemochromatosis protein, HFE, inhibits iron uptake via down-regulation of Zip14 in HepG2 cells. The Journal of Biological Chemistry2008; 283(31): 21462-21468. PMID: 18524764.