This research is aimed at elucidating the collective molecular events of cellular signaling that are initiated by plasma membrane immunoreceptors and are highly orchestrated in space and time. Focus is primarily on the high affinity receptor for IgE, Fc5RI, on mast cells, which plays a central role in the allergic immune response and serves as a valuable model system for these studies. The goal of these studies is to understand structural interactions of proteins and lipids occurring within the plasma membrane environment that are altered by antigen crosslinking of IgE-Fc5RI and result in transmembrane triggering of the intracellular signaling cascade. The central hypothesis is that interactions between crosslinked IgE-Fc5RI, Lyn kinase, and other early signaling components are coordinated within the heterogeneous structure of the membrane including its interactions with the cytoskeleton. Proposed studies will investigate the roles of dynamic membrane structure and interactions in Fc5RI signaling, and, in particular, the participation of ordered membrane domains (commonly called """"""""rafts"""""""").
Specific Aim 1 will continue to develop chemically modified substrates for patterning antigen on micro- and nanometer lengths scales, including use of thermosensitive polymers for rapidly triggered exposure of antigen. Spatially controlled, micron scale assemblies of co- clustered IgE-Fc5RI and cytoskeleton will be investigated as structures involved in initiation of internalization and phagocytosis.
Specific Aim 2 will examine spatial regulation and dynamics of IgE-Fc5RI-mediated signaling assemblies on the nanoscale with scanning electron microscopy and super high-resolution fluorescence microscopy, and apertures for near-field optical microscopy will be nanofabricated as a novel approach for measuring motional and interactional dynamics of individual membrane components. Together with data analysis, a theoretical framework will be developed to describe how clustered receptors synchronize their activation state via the membrane.
Specific Aim 3 will focus on participation of lipids in the membrane structural assemblies that spatially regulate IgE-Fc5RI mediated signaling using high resolution microscopies and electron spin resonance measurements of phase-like properties. Changes in proximity between Fc5RI and order- vs disorder- preferring lipids will be measured with fluorescence resonance energy transfer. Cholesterol distribution across the outer and inner leaflets of the plasma membrane will be assessed, and how perturbations of this distribution affect cell signaling events will be evaluated. These investigations integrate diverse physical, chemical and cell biological approaches to provide new insights into plasma membrane structure and dynamics and their roles in immunoreceptor signaling.
The heterogeneous plasma membrane millieu of eukaryotic cells maintains a steady state of protein and lipid interactions that support basal cell function and, while serving as a selective barrier, is poised to respond to environmental stimuli. Hijacking or disrupting these highly orchestrated membrane interactions is involved in numerous disease states, including pathogenic infection, neurodegeneration, and some cancers. In recent years the intricate participation of the plasma membrane in spatially regulating receptor-mediated signaling events has become increasingly appreciated. A prominent example is the receptor for IgE, Fc5RI, on mast cells, which plays a central role in the allergic immune response. The immediate goal of our studies is molecular level elucidation of the structural interactions occurring within dynamic plasma membrane domains that are altered by antigen crosslinking of IgE-Fc5RI and result in transmembrane triggering of the intracellular signaling cascade and immune cell responses. More generally, a detailed characterization of plasma membrane participation in cellular responses will provide new opportunities for intervention in therapeutic applications and a clearer understanding of the cell biology of health and disease.
|Holowka, David; Wilkes, Marcus; Stefan, Christopher et al. (2016) Roles for Ca2+ mobilization and its regulation in mast cell functions: recent progress. Biochem Soc Trans 44:505-9|
|Holowka, David; Baird, Barbara (2016) Roles for lipid heterogeneity in immunoreceptor signaling. Biochim Biophys Acta 1861:830-6|
|Sun, Chao; Wakefield, Devin L; Han, Yimo et al. (2016) Graphene Oxide Nanosheets Stimulate Ruffling and Shedding of Mammalian Cell Plasma Membranes. Chem 1:273-286|
|Holowka, David; Baird, Barbara (2015) Nanodomains in early and later phases of FcÉ›RI signalling. Essays Biochem 57:147-63|
|Jayant, Krishna; Singhai, Amit; Cao, Yingqiu et al. (2015) Non-Faradaic Electrochemical Detection of Exocytosis from Mast and Chromaffin Cells Using Floating-Gate MOS Transistors. Sci Rep 5:18477|
|Kelly, Christopher V; Wakefield, Devin L; Holowka, David A et al. (2014) Near-field fluorescence cross-correlation spectroscopy on planar membranes. ACS Nano 8:7392-404|
|Singhai, Amit; Wakefield, Devin L; Bryant, Kirsten L et al. (2014) Spatially defined EGF receptor activation reveals an F-actin-dependent phospho-Erk signaling complex. Biophys J 107:2639-51|
|Welch, M Elizabeth; Ritzert, Nicole L; Chen, Hongjun et al. (2014) Generalized platform for antibody detection using the antibody catalyzed water oxidation pathway. J Am Chem Soc 136:1879-83|
|Shelby, Sarah A; Holowka, David; Baird, Barbara et al. (2013) Distinct stages of stimulated FcÎµRI receptor clustering and immobilization are identified through superresolution imaging. Biophys J 105:2343-54|
|Welch, M Elizabeth; Xu, Youyong; Chen, Hongjun et al. (2013) Polymer Brushes as Functional, Patterned Surfaces for Nanobiotechnology. J Photopolym Sci Technol 25:53-56|
Showing the most recent 10 out of 81 publications