Ningning Zhao, PhD
Associate Professor, School of Nutritional Sciences and Wellness
EDUCATION & PROFESSIONAL TRAINING:
- 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
RESEARCH & INTERESTS:
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 firstname.lastname@example.org 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)
- Wu Y, Wei G, Zhao N*, Restriction of manganese intake prevents the onset of brain manganese overload in Zip14–/– mice, International Journal of Molecular Sciences, 2021; 22(13): 6773. PMID: 34202493. PMCID: PMC8268934.
- McCabe SM, Zhao N*, The potential roles of blood-brain barrier and blood-cerebrospinal fluid barrier in maintaining brain manganese homeostasis, Nutrients, 2021; 13(6). PMID: 34072120. PMCID: PMC8227615.
- Wei G, Wu Y, Zhao N*, Generation of a polyclonal antibody against the mouse metal transporter ZIP8, Antibodies, 2021; 10(2):16. PMID: 33919173. PMCID: PMC8167614.
- Morgan SE, Schroten H, Ishikawa H, Zhao N*, Localization of ZIP14 and ZIP8 in HIBCPP cells. Brain Sciences, 2020; 10(8): 534. PMID: 32784388. PMCID: PMC7464652.
- Winslow JWW, Limesand KH, Zhao N*, The functions of ZIP8, ZIP14, and ZnT10 in the regulation of systemic manganese homeostasis. International Journal of Molecular Sciences, 2020; 21(9): 3304. PMID: 32392784. PMCID: PMC7246657.
- Felber DF, Wu Y, Zhao N*, Regulation of metal transporter, ZIP14 and ZnT10, by manganese intake in mice. Nutrients, 2019, 11(9): 2099. PMID: 31487869. PMCID: PMC6770778.
- Scheiber IF, Alarcon NO°, Zhao N*, Manganese uptake by A549 cells is mediated by both ZIP8 and ZIP14. Nutrients, 2019; 11(7): 1473. PMID: 31261654. PMCID: PMC6682971.
- Scheiber IF, Wu Y, Morgan SE, Zhao N*, The intestinal metal transporter ZIP14 maintains systemic manganese homeostasis. The Journal of Biological Chemistry, 2019; 294(23): 9147-9160. PMID: 31028174. PMCID: PMC6556583.
- Zhao N*, Zhang AS, Wortham AM, Jue S, Knutson MD, and Enns CA, The Tumor Suppressor, P53, Decreases the Metal Transporter, ZIP14. Nutrients, 2017; 9 (12): 1335. PMID: 29292794. PMCID: PMC5748785.
- Wahedi M, Wortham AM, Kleven MD, Zhao N, Jue S, Enns CA, Zhang AS. 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. PMCID: PMC5672056.
- Zhao N, Maxson JE, Zhang RH, Wahedi M, Enns CA, and Zhang AS. Neogenin Facilitates the Induction of Hepcidin Expression by Hemojuvelin in the Liver. The Journal of Biological Chemistry, 2016; 291(23): 12322-12335. PMID: 27072365. PMCID: PMC4933279.
- Tuschl K, Meyer E, Valdivia LE, Zhao N, Dadswell C, Abdul-Sada A, Hung CY, Simpson MA, Chong WK, Jacques TS, et al. Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia. Nature Communications, 2016; 7:11601. PMID: 27231142. PMCID: PMC4894980.
- Zhao N, Nizzi CP, Anderson SA, Wang J, Ueno A, Tsukamoto H, Eisenstein RS, Enns CA and Zhang AS. Low intracellular iron increases the stability of matriptase-2. The Journal of Biological Chemistry, 2015; 290(7): 4432-4446. PMID: 25550162. PMCID: PMC4326848.
- Zhao N, Zhang AS, Worthen C, Knutson MD, and Enns CA. 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 America, 2014; 11(25): 9175-9180. PMID: 24927598. PMCID: PMC4078863.
- Zhao N, Zhang AS and Enns CA. Iron regulation by hepcidin. Journal of Clinical Investigation, 2013; 123 (6): 2337-2343. PMID: 23722909. PMCID: PMC3668831.
- Zhao N and Enns CA. N-linked glycosylation is required for transferrin-induced stabilization of transferrin receptor 2, but not for transferrin binding or trafficking to the cell surface. Biochemistry, 2013; 52: 3310-3319. PMID: 23556518. PMCID: PMC3656769.
- Zhao N and Enns CA. Iron transport machinery of human cells: players and their interactions. Current Topics in Membranes, 2012; 69: 67-93. PMID: 23046647. PMCID: PMC3934873.
- Pinilla-Tenas JJ, Sparkman BK, Shawki A, Illing AC, Mitchell CJ, Zhao N, Liuzzi JP, Cousins RJ, Knutson MD, 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 Physiology, 2011; 301(4): C862-71. PMID: 21653899. PMCID: PMC3191563.
- Zhao N, Gao J, Enns CA, Knutson MD. ZRT/IRT-like protein 14 (ZIP14) promotes the cellular assimilation of iron from transferrin. The Journal of Biological Chemistry, 2010; 285(42): 32141-32150. PMID: 20682781. PMCID: PMC2952215.
- Gao J, Zhao N, Knutson MD, Enns CA. The hereditary hemochromatosis protein, HFE, inhibits iron uptake via down-regulation of ZIP14 in HepG2 cells. The Journal of Biological Chemistry, 2008; 283(31): 21462- 21468. PMID: 18524764. PMCID: PMC2490774.