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Published on: October 15, 2014
A functional ryanodine-sensitive intracellular Ca2+ store is present in vascular endothelial cells
R C Ziegelstein1, H A Spurgeon, R Pili
1Laboratory of Cardiovascular Science, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224.
Functional ryanodine-sensitive calcium (Ca2+) stores exist in vascular endothelial cells. These stores regulate intracellular Ca2+ storage and release, impacting cellular responses.
Area of Science:
- Cardiovascular Biology
- Cell Physiology
- Endothelial Cell Function
Background:
- The ryanodine receptor (RyR) presence in vascular endothelium is known, but its functional role remains unclear.
- Intracellular calcium (Ca2+) signaling is critical for endothelial cell function.
- Understanding Ca2+ regulation in endothelial cells is vital for cardiovascular health.
Purpose of the Study:
- To determine the presence of functional ryanodine-sensitive Ca2+ stores in various cultured vascular endothelial cells.
- To investigate the role of these stores in intracellular Ca2+ regulation and endothelial cell responses.
Main Methods:
- Primary cultured endothelial cells from rat aorta (RAECs), human aorta (HAECs), human umbilical vein (HUVECs), and bovine pulmonary artery (BPAECs) were used.
- Indo 1 fluorescence was employed to measure intracellular Ca2+ changes.
- Cells were exposed to ryanodine and various agonists (bradykinin, histamine) under different extracellular Ca2+ concentrations.
Main Results:
- HAECs, BPAECs, and HUVECs showed a slow intracellular Ca2+ increase with ryanodine at rest; RAECs did not.
- Ryanodine blunted the Ca2+ response to a second bradykinin exposure in RAECs.
- Higher extracellular Ca2+ concentrations enhanced ryanodine's effect on agonist-induced Ca2+ release in HUVECs.
Conclusions:
- Functional ryanodine-sensitive Ca2+ stores are present in vascular endothelial cells.
- These stores are involved in regulating Ca2+ storage and release from agonist-sensitive intracellular compartments.
- Ryanodine receptor activity in endothelial cells influences intracellular Ca2+ dynamics.
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