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May 27, 2021
11 a.m. EDT
Epithelial cells line mucosal surfaces. In the intestine, the epithelium separates—and therefore regulates—interactions between the immune system and luminal materials, including dietary antigens and microbes. In the absence of specific transporters, epithelial cell membranes are nearly impermeant to hydrophilic materials. However, the ultimate success of the barrier depends on the ability of epithelial cells to prevent unrestricted paracellular flux across the shunt pathway. Intercellular tight junctions form selectively permeable seals that mediate paracellular flux.
The biophysical characteristics of these tight junction seals are modulated during development and by physiological stimuli, immune cell signaling and enteric pathogens. In turn, tight junction-selective permeability modifies nutrient transport, mucosal immune tone and pathogen clearance. Recent advances have shed new light on the mechanisms of tight junction regulation and the impact of barrier modulation on mucosal homeostasis and health, pathogenic progression and resolution of disease.
Learning objectives to be explored in this webinar include:
- Tissue barriers are dynamic and selectively permeable.
- Barrier function can be regulated by one tight junction-independent and two distinct tight junction-dependent mechanisms.
- The immune system selectively activates specific trans-tight junction flux pathways.
- Subtle changes in mucosal homeostasis induced by barrier modulation can markedly impact overall health.
Presenter
The research of Jerrold Turner, MD, PhD, of Brigham and Women’s Hospital in Boston, is focused on how epithelia establish, maintain and regulate barriers. This fundamental property is essential for survival of multicellular organisms and allows controlled interactions with the external environment and compartmentalization of distinct tissues. The structure that maintains these barriers and regulates flux between cells is the tight junction. Turner’s laboratory takes a multidisciplinary approach that integrates cell and developmental biology, transport physiology, electrophysiology, structural biology, molecular biology and mucosal immunology to define fundamentals of structure and function; to understand mechanisms of regulation in vitro and in vivo models; to determine the contributions of barrier dysfunction to gastrointestinal disease; to understand the role of the epithelial barrier in regulating other mucosal processes, (e.g., immune responses); and to develop novel means to correct barrier function and restore health.
