James Martin, MD

Primary Axis: 
Respiratory Health
Research Focus: 

Airway inflammation in asthma is a T cell-driven process. The extent of inflammation is controlled by several T cell subsets. Using animal models, we have investigated the contributions of CD4+ T cells and various CD8+ T cell subsets, both αβ-TCR and γδ-TCR+ cells in asthma. Currently the role of the T cell in causing structural remodeling of the airways, and in particular airway smooth muscle growth, is being addressed. A combination of whole animal and cellular models is being used to address mechanisms of remodeling and the growth factors that may be implicated. The effects of airway inflammation on airway smooth muscle contractile properties are also being addressed. It is hoped that these studies will help to clarify the complex interactions between T cell-driven inflammation and abnormal proliferation of smooth muscle in asthmatic airways.Asthma, airway inflammation, Th2 cells, T cell cytokines, airway smooth muscle culture, calcium signaling, single cell imaging, lung morphometry, animal models

Keywords: 
Asthma, airway inflammation, Th2 cells, T cell cytokines, airway smooth muscle culture, calcium signaling, single cell imaging, lung morphometry, animal models
Location: 
Meakins-Christie Laboratories
Publications:
Moynihan B, Tolloczko B, Michoud MC, Tamaoka M, Ferraro P, Martin JG. MAP kinases mediate interleukin-13 effects on calcium signaling in human airway smooth muscle cells. Amer J Physiol (In press) 2008.
Ramos-Barbón D, Presley JF, Hamid QA, Fixman ED, Martin JG. Antigen-specific CD4+ T cells drive airway smooth muscle remodeling in experimental asthma. Journal of Clinical Investigation 115: 1580-1589; 2005.
Smith BA, Tolloczko B, Martin JG, Grutter P. Probing the viscoelastic structure of cultured airway smooth muscle cells with atomic force microscopy: MLCK-independent stiffening induced by contractile agonist. Biophysical Journal 88(4): 2994-3007; 2005.