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Updated: Jul 17, 2026

Simultaneous Measurements of Intracellular Calcium and Membrane Potential in Freshly Isolated and Intact Mouse Cerebral Endothelium
Published on: January 20, 2019
Heterogeneous cytoplasmic calcium response in microvascular endothelial cells.
D Hong1, K A Barbee, D G Buerk
1School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, 19104, USA.
Calcium signaling in rat endothelial cells shows heterogeneity. ATP and shear stress trigger calcium waves, mediated by purinergic receptors and influenced by ATP concentration and receptor distribution.
Area of Science:
- Endothelial cell biology
- Calcium signaling
- Vascular physiology
Background:
- Endothelial cells play a crucial role in vascular function.
- Calcium (Ca2+) signaling is fundamental to cellular processes.
- Heterogeneity in cellular responses can impact tissue-level function.
Purpose of the Study:
- To investigate calcium concentration changes in response to ATP and shear stress in rat adrenomedullary endothelial cells (RAMECs).
- To elucidate the mechanisms underlying heterogeneous calcium responses and wave propagation.
Main Methods:
- Cultured rat adrenomedullary endothelial cells (RAMECs) were used.
- Changes in intracellular calcium concentration ([Ca2+]i) were monitored.
- Responses to exogenous ATP and induced shear stress were analyzed.
- The effect of suramin, a purinergic receptor blocker, was assessed.
Main Results:
- A significant heterogeneity in spatial and temporal calcium responses was observed.
- Shear stress and exogenous ATP induced calcium waves propagating between cells.
- Wave propagation was dependent on ATP concentration and suppressed by suramin.
- Heterogeneous purinergic receptor distribution was identified as a key factor in response variability.
Conclusions:
- ATP acts as an autocrine and paracrine mediator in RAMECs.
- Purinergic receptors mediate calcium wave propagation initiated by ATP or shear stress.
- Heterogeneous purinergic receptor distribution contributes to coordinated vascular function through integrated cellular responses.
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