Lee Ligon

Associate Dean of Science for Academic Affairs, Biological Sciences

In the Ligon lab, we are interested in how cells function in the three-dimensional world. We study the internal structure of the cell, the cytoskeleton, and how it is organized to generate and maintain the complex 3D shape of differentiated cells. We also study how cells interact with their environment, in particular how cancer cells interact with the tissue surrounding the tumor, also known as the tumor microenvironment. We use a combination of live-cell imaging and other cell biological, biochemical and molecular techniques to examine cell structure, dynamics and function in the context of the living cell. Some cells, such as those of the nervous system, have elaborate three-dimensional shapes that are essential to their specialized activities. We study the microtubule cytoskeleton, a complex network of protein polymers that are essential to establish and maintain cell structure. Microtubules have several functions in the cell: they are mechanical and structural elements; they serve as tracks for long-distance movements of organelles and other cargoes; and they can play a direct role in biochemical signaling cascades. We are investigating how certain sub-populations of microtubules are biochemically specialized for specific cellular functions by a combination of sub-cellular location, post-translational modifications, and interactions with other proteins. We are also investigating the role of the tumor microenvironment in the metastatic progression of cancer cells. Both the cells and the non-cellular elements of the tissue surrounding a tumor can play a significant role in whether or not a tumor cell will become invasive. We are using the tools of cell biology and biochemistry, as well as novel biomimetic materials, to explore the role of abnormal cell-cell interactions and cell-matrix interactions in a breast cancer model system.

Outside of the lab, I am very involved in efforts to advance diversity, equity and inclusion in science. I serve as the co-chair of the RPI LGBTQ+ Task Force, as well as the co-chair of the LGBTQ+ Task Force for the American Society for Cell Biology. I am also involved in efforts to promote effective scientific outreach, communication, and evidence-based policy, and serve as the co-chair of the Public Information Committee for the American Society for Cell Biology.


Ph.D. University of Virginia Neuroscience Postdoctoral training, University of Pennsylvania Cell Biology, Biochemistry

Research Focus
  • Cell Biology
  • Neurosocience
Select Works
  • Bogorodskaya D, McLane JS, Ligon LA. Dual-matrix 3D culture system as a biomimetic model of epithelial tissues. [preprint]. 2019 March; Available from: https://www.biorxiv.org/content/10.1101/594549v1. doi: 10.1101/594549
  • Bogorodskaya D, Ligon LA. Septins Coordinate with Microtubules and Actin to Initiate Cell Morphogenesis. [preprint]. 2019 March; Available from: https://www.biorxiv.org/content/10.1101/594515v1. doi: 10.1101/594515
  • McLane JS, Ligon LA. Stiffened Extracellular Matrix and Signaling from Stromal Fibroblasts via Osteoprotegerin Regulate Tumor Cell Invasion in a 3-D Tumor in Situ Model. Cancer Microenviron. 2016 Dec;9(2-3):127-139. doi: 10.1007/s12307-016-0188-z. Epub 2016 Sep 21.
  • DiLorenzo T, Ligon L, Drew D. Determination of Statistical Properties of Microtubule Populations. Appl Math (Irvine). 2016 Aug;7(13):1456-1475. doi: 10.4236/am.2016.713125. Epub 2016 Aug 15.
  • McLane JS, Ligon LA. Palladin Mediates Stiffness-Induced Fibroblast Activation in the Tumor Microenvironment. Biophys J. 2015 Jul 21;109(2):249-64. doi: 10.1016/j.bpj.2015.06.033. PMID: 26200861
  • McLane JS, Rivet CJ, Gilbert RJ, Ligon LA. A biomaterial model of tumor stromal microenvironment promotes mesenchymal morphology but not epithelial to mesenchymal transition in epithelial cells. Acta Biomater. 2014 Jul 22. pii: S1742-7061(14)00310-9. doi: 10.1016/j.actbio.2014.07.016.
  • McLane JS, Schaub NJ, Gilbert RJ, Ligon LA. Electrospun nanofiber scaffolds for investigating cell-matrix adhesion. Methods Mol Biol. 2013;1046:371-88. doi: 10.1007/978-1-62703-538-5_23. 10.1007/978-1-62703-538-5_23. PubMed PMID: 23868601.
  • Apostolopoulou M, Ligon L. Cadherin-23 mediates heterotypic cell-cell adhesion between breast cancer epithelial cells and fibroblasts. PLoS One. 2012;7(3):e33289. doi: 10.1371/journal.pone.0033289. Epub 2012 Mar 7.