Weiquan (Wendy) Zhu
Adjunct Associate Professor of Microbiology & Immunology and Associate Professor of Ophthalmology & Visual Sciences
Vascular Biology, Cell Biology, Neuroinflammatory Diseases, and Aging

Molecular Biology Program
Education
B.S. Yancheng Teachers University
M.S. Nanjing Normal University
Ph.D. Chinese Academy of Medical Sciences & Peking Union Medical College
Research
Our lab investigates the critical role of vascular dysfunction in the onset and progression of inflammatory diseases and aging, particularly within the central nervous system (CNS), including the retina. My research journey began during my postdoctoral training, where I focused on identifying pathways that compromise vascular stability—a key factor in both acute and chronic inflammatory conditions such as sepsis, influenza, and arthritis. As an independent investigator, I expanded my research to encompass neuroinflammatory diseases. The primary objective of my lab is to elucidate how vascular instability drives disease pathology and to uncover potential therapeutic targets for conditions like Age-related Macular Degeneration, Diabetic Retinopathy, Multiple Sclerosis, and Alzheimer's Disease.
Our lab made a significant breakthrough by identifying that inflammation-induced endothelial-to-mesenchymal transition (EndoMT) within the CNS disrupts the blood-CNS barrier (BCNSB), playing a crucial role in the pathogenesis and progression of neuroinflammatory diseases, particularly multiple sclerosis (MS). We found that inhibiting EndoMT not only prevents vascular damage but also promotes remyelination and functional recovery in MS animal models, all without compromising the immune system—a notable challenge in current MS therapies. These findings open promising new avenues for therapeutic interventions in MS and potentially other neuroinflammatory diseases.
References
- Sun Z, Zhao H, Fang D, Davis CT, Shi DS, Lei K, Rich BE, Winter JM, Guo L, Sorensen LK, Pryor RJ, Zhu N, Lu S, Dickey LL, Doty DJ, Tong Z, Thomas KR, Mueller AL, Grossmann AH, Zhang B, Lane TE, Fujinami RS, Odelberg SJ, Zhu W. Neuroinflammatory disease disrupts the blood-CNS barrier via crosstalk between proinflammatory and endothelial-to-mesenchymal-transition signaling. 2022 Oct 5;110(19):3106-3120.e7. doi: 10.1016/j.neuron.2022.07.015. Epub 2022 Aug 11. PubMed PMID: 35961320; PubMed Central PMCID: PMC9547934.
- Pei J, Cai L, Wang F, Xu C, Pei S, Guo H, Sun X, Chun J, Cong X, Zhu W, Zheng Z, Chen X. LPA(2) Contributes to Vascular Endothelium Homeostasis and Cardiac Remodeling After Myocardial Infarction. Circ Res. 2022 Aug 19;131(5):388-403. doi: 10.1161/CIRCRESAHA.122.321036. Epub 2022 Aug 3. PubMed PMID: 35920162.
- Zhu W, Shi DS, Winter JM, Rich BE, Tong Z, Sorensen LK, Zhao H, Huang Y, Tai Z, Mleynek TM, Yoo JH, Dunn C, Ling J, Bergquist JA, Richards JR, Jiang A, Lesniewski LA, Hartnett ME, Ward DM, Mueller AL, Ostanin K, Thomas KR, Odelberg SJ, Li DY. Small GTPase ARF6 controls VEGFR2 trafficking and signaling in diabetic retinopathy. J Clin Invest. 2017 Dec 1;127(12):4569-4582. doi: 10.1172/JCI91770. Epub 2017 Oct 23. PubMed PMID: 29058688; PubMed Central PMCID: PMC5707163.
- Zhu W, London NR, Gibson CC, Davis CT, Tong Z, Sorensen LK, Shi DS, Guo J, Smith MC, Grossmann AH, Thomas KR, Li DY. Interleukin receptor activates a MYD88-ARNO-ARF6 cascade to disrupt vascular stability. 2012 Dec 13;492(7428):252-5. doi: 10.1038/nature11603. Epub 2012 Nov 11. PubMed PMID: 23143332; PubMed Central PMCID: PMC3521847.
- London NR, Zhu W, Bozza FA, Smith MC, Greif DM, Sorensen LK, Chen L, Kaminoh Y, Chan AC, Passi SF, Day CW, Barnard DL, Zimmerman GA, Krasnow MA, Li DY. Targeting Robo4-dependent Slit signaling to survive the cytokine storm in sepsis and influenza. Sci Transl Med. 2010 Mar 17;2(23):23ra19. doi: 10.1126/scitranslmed.3000678. PubMed PMID: 20375003; PubMed Central PMCID: PMC2875996.