Research Bio
In exocrine acinar cells regulation of intracellular calcium plays a pivotal role in controlling fluid and protein secretion. Exposure of cells to neurotransmitters and hormones results in a rapid elevation of intracellular calcium. This increase in [Ca2+]i carries complex spatial and temporal information important to the physiology of the acinar cell. Research in this laboratory focuses on gaining a better understanding of the mechanisms which underlie these signaling patterns with a primary goal of relating this knowledge to the physiology and pathophysiology of exocrine cells.
Although all Ca2+ mobilizing agonists in pancreatic acinar cells utilize the phosphoinositide-signaling (PI) pathway, stimulation by individual agents results in markedly different temporal and spatial patterns of Ca2+ signaling. One project is designed to understand at the molecular level how the cell effectively "knows"
which PI-coupled agonist it is currently exposed to. Given that tremendous molecular diversity is expressed at all levels of this signaling pathway, our working hypothesis is that individual agonists do not couple to the signaling machinery in an identical fashion. This study involves precisely defining by molecular techniques the individual signaling proteins expressed in the acinar cell and then subsequently assessing if individual agonists utilize discrete and different elements of the PI-signaling pathway. We are utilizing fluorescence imaging techniques including high-speed confocal microscopy to monitor [Ca2+]i while manipulating the signaling pathway with neutralizing antibodies and antisense technology.
A further project relates to the organization and regulation of calcium release sites in exocrine cells. These organelles are defined by the expression of receptors for the second messenger Inositol 1,4,5-trisphosphate. In acinar cells the distribution of these receptors is tightly localized to an area associated with the actin cytoskeleton in the apical secretory pole of the cell. This distribution of receptors is the major factor in defining the spatial characteristics of the Ca2+ signal. The nature of the association with the cytoskeleton is being investigated. In addition the regulation of these receptors by phosphorylation and the consequences this may have for Ca2+ signaling are also being studied.
2012 Apr 30
Wagner LE, Yule DI. "Differential regulation of the InsP3 receptor type-1 and -2 single channel properties by InsP3, Ca2+ and ATP." The Journal of physiology. 2012 Apr 30; Epub 2012 Apr 30. |
2012 Apr 14
Palk L, Sneyd J, Patterson K, Shuttleworth TJ, Yule DI, Maclaren O, Crampin EJ. "Modelling the effects of calcium waves and oscillations on saliva secretion." Journal of theoretical biology. 2012 Apr 14; 305CEpub 2012 Apr 14. |
2012 Apr 10
Bhattacharya S, Verrill DS, Carbone KM, Brown S, Yule DI, Giovannucci DR. "Distinct Contributions By Ionotropic Purinoceptor Subtypes To ATP-Evoked Calcium Signals In Mouse Parotid Acinar Cells." The Journal of physiology. 2012 Apr 10; Epub 2012 Apr 10. |
2012 Feb
Almassy J, Won JH, Begenisich TB, Yule DI. "Apical Ca2+-activated potassium channels in mouse parotid acinar cells." The Journal of general physiology. 2012 Feb 0; 139(2):121-33. |
2012 Jan
Park HS, Betzenhauser MJ, Zhang Y, Yule DI. "Regulation of Ca²? release through inositol 1,4,5-trisphosphate receptors by adenine nucleotides in parotid acinar cells." American journal of physiology. Gastrointestinal and liver
physiology. 2012 Jan 0; 302(1):G97-G104. Epub 2011 Sep 29. |
