Guangwei Du, PhD

  • Professor
 
Contact
Guangwei Du, PhD
713-500-7055
713-500-0689 fax

Education

Postdoctoral Fellow
Stony Brook University, 2002
Ph.D.
Peking Union Medical College & Chinese Academy of Medical Sciences, China, 1998
M.S.
Wuhan University, 1995
B.S.
Wuhan University, 1992

Areas of Interest

Research Interests

The Du laboratory seeks to understand the fundamental principles that govern the organization and function of living cells. We investigate how intracellular organelles communicate, how membrane systems coordinate signaling and metabolism, and how these processes allow cells to maintain homeostasis and adapt to changing physiological conditions. A major focus of our research is understanding how lipid signaling and lipid metabolism regulate cellular behavior, organelle function, and tissue physiology. By addressing these fundamental questions, we aim to gain new insights into the mechanisms that underlie human health and disease.

Using a multidisciplinary approach that combines cell biology, biochemistry, molecular genetics, advanced imaging, and analysis of human patient datasets, we study how organelles such as lysosomes, mitochondria, the endoplasmic reticulum, and the Golgi apparatus function as an integrated network within cells. We are particularly interested in how lipids act not only as structural components of membranes but also as signaling molecules that coordinate intracellular communication, metabolic adaptation, membrane trafficking, and stress responses. We are also committed to developing innovative tools that enable researchers to study organelle biology, lipid metabolism, and intracellular signaling with greater precision and resolution.

A defining feature of our research program is the integration of mechanistic studies in cultured cells, physiologically relevant mouse models, and human data analysis. This approach allows us to uncover molecular mechanisms, determine their physiological significance in vivo, and evaluate their relevance to human disease. By bridging these complementary systems, we seek to understand how disruptions in organelle function, lipid metabolism, and cellular signaling contribute to cancer, aging, metabolic disorders, neurodegeneration, and other diseases.

Our long-term goal is to translate fundamental discoveries in cell biology into new therapeutic opportunities. We believe that a deeper understanding of how cells organize their internal architecture, coordinate metabolic activities, and respond to physiological stress will reveal novel strategies for preventing and treating disease. By identifying the cellular pathways that become dysregulated in human disorders, we hope to uncover new therapeutic targets and contribute to the development of more effective treatments that improve human health.

Publications

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  1. Luu TTT, Zhang D, Bheemanapally K, Zaman M, Wu Z, Liu Y, Wu X, Kim HE, Zheng L, Ogretmen B, Peng J, Du G. (2026). Proteome Responses to Acute Inhibition of De Novo Sphingolipid Synthesis Suggest Cancer Combination Therapies. Cancers (Basel). 18(11). PMID: 42279409; PMCID: PMC13256006.
  2. Zheng L, Niu W, Xie X, Vu T, Du G. (2026). A redox-sensitive phosphatase regulates glycolysis as a metabolic switch in the bacterial inner membrane. Sci Adv. 12(19):eaea8724. PMID: 42090508; PMCID: PMC13148334.
  3. Adachi Y, Torres M, Hunter AH, Cho WJ, Pan M, Han X, Du G, Qi L, Iijima M, Sesaki H. (2025). AGPAT2 acts at the crossroads of lipid biosynthesis and DRP1-mediated ER morphogenesis. Nat Commun. 16(1):11473. PMID: 41387688; PMCID: PMC12749901.
  4. Cai M, Wang Z, Luu TTT, Zhang D, Finke B, He J, Tay LWR, Di Paolo G, Du G*. (2022). PLD1 promotes reactive oxygen species production in vascular smooth muscle cells and injury-induced neointima formation. Biochim Biophys Acta Mol Cell Biol Lipids. 1867(1):159062. PMID: 34610470.
  5. Xiong J, He J, Xie WP, Hinojosa E, Ambati CSR, Putluri N, Kim HE, Zhu MX, Du G. (2019). Rapid affinity purification of intracellular organelles using twin strep tag. J Cell Sci. 132(24). pii: jcs235390. PMCID: PMC6955222.
  6. Wang Z, Cai M, Tay LWR, Zhang F, Wu P, Huynh A, Cao X, Di Paolo G, Peng J, Milewicz DM, Du G. (2019). Phosphatidic acid generated by PLD2 promotes the plasma membrane recruitment of IQGAP1 and neointima formation. FASEB J. 33(6):6713-6725. PMCID: PMC6529346.
  7. He J, Zhang F, Tay LW, Boroda S, Nian W, Levental KR, Levental I, Harris TE, Chang JT, Du G. (2017). Lipin-1 regulation of phospholipid synthesis maintains endoplasmic reticulum homeostasis and is critical for triple-negative breast cancer cell survival. FASEB J. 130(12):2007-2017. PMID: 28347999.
  8. Han B, Sivaramakrishnan P, Lin CJ, Neve IAA, He J, Tay LWR, Sowa JN, Sizovs A, Du G, Wang J, Herman C, Wang MC. (2017). Microbial Genetic Composition Tunes Host Longevity. Cell. 169(7):1249-1262. PMCID: PMC5635830.
  9. Wang Z, Zhang F, He J, Wu P, Tay LWR, Cai M, Nian W, Weng Y, Qin L, Chang JT, McIntire LB, Di Paolo G, Xu J, Peng J, Du G. (2017). Binding of PLD2-generated phosphatidic acid to KIF5B promotes MT1-MMP surface trafficking and lung metastasis of mouse breast cancer cells. Developmental Cell. 43(2):186-197. PMCID: PMC5663201.
  10. Cai M, He J, Xiong J, Tay LWR, Wang Z, Rog C, Wang, J, Xie Y, Wang G, Banno Y, Li F, Zhu M, Du G. (2016). Phospholipase D1-regulated autophagy supplies free fatty acids to counter nutrient stress in cancer cells. Cell Death & Disease. 7(11):e2448. PMCID: PMC5260880
  11. Zhang F, Wang Z, Lu M, Yonekubo Y, Liang X, Zhang Y, Wu P, Zhou Y, Grinstein S, Hancock JF, Du G. (2014). Temporal production of the signaling lipid phosphatidic acid by phospholipase D2 determines the output of ERK signaling in cancer cells. Mol Cell Biol. 34(1):84-95. PMCID: PMC3911278.