Key result
Endothelial Ca2+ signaling is a continuum in which specific store-release components and cellular targets allow for differential modes of signal expansion and distinctive effector recruitment profiles.
This review highlights the complex, dynamic nature of endothelial calcium signaling and its role in regulating arterial tone and vascular function.
Supports detailed endothelial Ca2+ models in vascular research; extends mechanistic knowledge while leaving clinical translation open.
The endothelium is vital to normal vasoregulation. Although acute vasodilation associated with broad endothelial Ca(2+) elevation is well known, the control and targeting of Ca(2+) -dependent signals in the endothelium are poorly understood. Recent studies have revealed localized IP(3) -motivated Ca(2+) events occurring basally along the intima that may provide the fundamental basis for various endothelial influences. Here, we provide an overview of dynamic endothelial Ca(2+) signals and discuss the potential role of these signals in constant endothelial control of arterial tone and the titration of functional responses in vivo. In particular, we focus on the functional architecture contributing to the properties and ultimate impact of these signals, and explore new avenues in evaluating their prevalence and specific modalities in intact tissue. Finally, we discuss spatial and temporal effector recruitment through modification of these inherent signals. It is suggested that endothelial Ca(2+) signaling is a continuum in which the specific framework of store-release components and cellular targets along the endothelium allows for differential modes of Ca(2+) signal expansion and distinctive profiles of effector recruitment. The precise composition and distribution of these inherent components may underlie dynamic endothelial control and specialized functions of different vascular beds.
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Taylor et al. (2012) conducted a review in Vascular endothelial function. Endothelial Ca2+ signaling is a continuum in which specific store-release components and cellular targets allow for differential modes of signal expansion and distinctive effector recruitment profiles.
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