Robert Saxton

Contact

University of California, Berkeley 175 Li Ka Shing Center #3370 Berkeley, CA 94720-3370
Title: 
Assistant Professor of Chemistry and of Immunology and Molecular Medicine
Department: 
Chemistry
Molecular and Cell Biology (MCB)
Research: 

Mechanisms of cell signaling controlling tissue inflammation, repair, and homeostasis.

Research

Inflammatory immune responses are essential for protecting organisms against infection and disease. However, excessive inflammation can damage bystander tissues and compromise biological function. To prevent this, mammals have evolved a complex array of signaling molecules and receptors that ensure the protection and repair of host tissues. Failure of these homeostatic systems can result in chronic inflammation, autoimmunity, and cancer — diseases with rapidly increasing prevalence in modern society.

The Saxton lab studies the molecular mechanisms of cell communication underlying tissue inflammation, repair, and homeostasis, with the goal of developing novel therapeutics to modulate these pathways in disease. To do this, the Saxton lab uses a range of biochemical and structural biology techniques, together with cutting edge approaches in protein engineering, receptor pharmacology, and mouse models of inflammation, in order to understand and control inflammatory signaling at the atomic, cellular, and organismal levels.

Robert Saxton research graphic

Project Areas

  1. Resolution of inflammation
    The resolution of inflammation is essential for returning to homeostasis following tissue damage, and persistent, unresolved inflammation is a central feature of nearly all human diseases. We seek to understand the signaling mechanisms that enable the efficient resolution of inflammation in order exploit these processes therapeutically. Our previous work has focused on the key anti-inflammatory cytokine interleukin-10 (IL-10), where we have used the cryo-EM structure of the IL-10 receptor complex to rationally design cell type selective IL-10 variants with enhanced therapeutic properties. These molecules are currently being developed for clinical use in autoimmune and chronic inflammatory disease.
  2. Mechanisms of immune-mediated tissue repair
    In addition to eliminating infectious agents, cells of the immune system also play key roles in repairing tissues following damage caused by either pathogens or the immune system itself. This role is particularly critical at epithelial barriers of the GI tract, skin, and lungs, which are constantly exposed to microbes and environmental damage. By understanding the mechanisms of immune-epithelial crosstalk that promote tissue repair, we hope to develop novel protein therapeutics that drive repair and promote mucosal healing in the context of diseases including IBD, psoriasis, and GvHD.
  3. Metabolic signals that modulate immune function
    Metabolic dysfunction such as in obesity or type 2 diabetes strongly predisposes for chronic inflammatory disorders and several types of cancer. Although it is clear that many aspects of immune function are regulated by metabolic signals (e.g. hormones, metabolites), the molecular mechanisms through which these signals modulate inflammation remain poorly understood. By studying the ligand-receptor systems that mediate metabolic-immune crosstalk we hope to identify new routes of controlling and preventing diseases associated with metabolic dysfunction.