Joel Swanson, PhD
Microbiology and Immunology
1550 West Medical Center Drive
Ann Arbor, MI 48019-5620
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Qualifications
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Post-doctoral FellowColumbia University College of Physicians and Surgeons, Physiology, New York, United States
1984 - 1986
Postdoctoral Fellowship
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Post-doctoral FellowRockefeller University, Cellular Physiology, New York, United States
1982 - 1984
Postdoctoral Fellowship
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PhDPrinceton University, Princeton, NJ, United States
1978 - 1982
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MSOhio State University, Columbus, OH, United States
1976 - 1978
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BARutgers University, New Brunswick, NJ, United States
1971 - 1975
Research Overview
Dr. Swanson has devoted much of his research career to understanding the mechanisms and regulation of macropinocytosis and phagocytosis in macrophages, processes which require the actin cytoskeleton and extensive membrane trafficking. His lab developed novel experimental methods for analyzing chemistry and molecular dynamics inside living cells and applied them to investigate a wide range of questions in cell biology and innate immunity. His research has concentrated recently on mechanisms of signal transduction underlying phagocytosis and macropinocytosis, as well as the dynamics of endocytic compartments. His lab developed novel microscopic methods to measure protein-protein interactions by FRET, the dynamics of cyclic AMP and the GTPases Rac, Cdc42, Arf1, Arf6 and Rab5 in living cells, the magnitude of signals in forming phagosomes and the timing of signal amplification relative to phagosome and macropinosome closure. Current projects address mechanisms of macropinosome formation and traffic within cells, and the role of nutrients in the regulation of micropinocytosis, and the role of micropinocytosis in cell growth.
Links
J. Swanson Lab
Recent Publications
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Neupane A, Wollman JW, Donahoe J, Pradhan B, Balster JJ, Poudel S, Waniarachchi K, Hoppe AD, Swanson JA, Scott BL, Thiex NW. 2026 Sep 9; bioRxiv,PreprintPI(3)P Signaling by VPS34 Complex II Orchestrates Macropinocytosis
DOI:10.64898/2026.09.03.749235 -
Neupane A, Balster J, Donahoe J, Dorn N, Hoppe A, Pradhan B, Scott B, Poudel SS, Swanson J, Thiex N, Wollman J, Yin P. The Journal of Immunology, 2026 Jul 29; 215 (Supplement_1): vkag141.715Journal ArticleUVRAG and the VPS34 complex II regulate macropinocytosis via the synthesis of PI(3)P on the plasma membrane 2259463
DOI:10.1093/jimmun/vkag141.715 -
Manivannan P, Santos da Costa C, Tang Y, Wang X, Swanson J, Murakami T, Ono A, King PD. 2026 Apr 28;PreprintThe gp120 Envelope Glycoprotein of HIV-1 Triggers Macropinocytosis in Primary CD4+ T Cells to Promote HIV-1 Infection.
DOI:10.64898/2026.04.27.721102 PMID: 42094527 -
Tebeje BM, Hoppe AD, Thiex NW, Swanson JA. Journal of Cell Science, 2026 Jan 1; 139 (2):Journal ArticleMacropinocytosis facilitates amino acid acquisition from extracellular fluid to support cell proliferation in macrophages
DOI:10.1242/jcs.264398 PMID: 41439336 -
Thiex NW, Neupane A, Wollman J, Pradhan B, Donahoe J, Balster J, Poudel S, Scott B, Swanson J. The Journal of Immunology, 2025 Nov 23; 214 (Supplement_1):Journal ArticleCRISPR/Cas9 whole genome screen identifies UVRAG and members of VPS34 complex II as regulators of macrophage macropinocytosis 4573
DOI:10.1093/jimmun/vkaf283.2241 -
Murakami T, de Souza Cardoso R, Manivannan P, Chang YT, Rentchler E, Chou KN, Tang Y, Swanson JA, King PD, Ono A. Proceedings of the National Academy of Sciences of the United States of America, 2025 Jun 10; 122 (23):Journal ArticleMacropinosomes are a site of HIV-1 entry into primary CD4+ T cells
DOI:10.1073/pnas.2417676122 PMID: 40465625 -
Murakami T, de Souza Cardoso R, Manivannan P, Chang Y-T, Rentchler E, Chou K-N, Tang Y, Swanson JA, King PD, Ono A. 2025 Mar 12; bioRxiv,PreprintMacropinosomes are a site of HIV-1 entry into primary CD4+ T cells
DOI:10.1101/2025.03.07.642068 -
Tebeje BM, Thiex NW, Swanson JA. 2024 Oct 22;PreprintGrowing Macrophages Regulate High Rates of Solute Flux by Pinocytosis.
DOI:10.1101/2024.10.22.619691 PMID: 39484410
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