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Published on: May 20, 2012
Magnesium and microvascular endothelial cells: a role in inflammation and angiogenesis
Daniela Bernardini1, Anna Nasulewic, Andrzej Mazur
1University of Milan, Department of Preclinical Sciences-LITA Vialba, Milano, Italy.
Abstract:
Microvascular endothelial cells are protagonists in inflammation and angiogenesis. Since magnesium (Mg) deficiency promotes inflammation and impairs angiogenesis in vivo, we evaluated the effect of different concentrations of the cation on microvascular 1G11 cells. We found that low Mg inhibits endothelial growth and migration, while it increases some inflammatory markers. In particular we show that low Mg stimulates the synthesis of interleukin 1a and 6, of nitric oxide, a mediator of inflammatory responses, and of VCAM, which mediates monocyte/endothelial interactions. On the contrary, high Mg stimulates proliferation and migration and sensitizes microvascular cells to migratory signals, thus inducing crucial events in angiogenesis. Our results demonstrate a direct role of Mg in modulating microvascular functions and provide a molecular explanation to the link among Mg, angiogenesis and inflammation observed in in vivo models.
Insights
Magnesium (Mg) impacts microvascular endothelial cell function. Low Mg inhibits growth and increases inflammation, while high Mg promotes proliferation and migration, crucial for angiogenesis.
Area of Science:
- Cell Biology
- Physiology
- Biochemistry
Background:
- Microvascular endothelial cells are key players in inflammation and angiogenesis.
- Magnesium (Mg) deficiency is linked to increased inflammation and impaired angiogenesis in vivo.
- Understanding Mg's role at the cellular level is crucial.
Purpose of the Study:
- To investigate the effects of varying magnesium concentrations on microvascular endothelial cell function.
- To elucidate the molecular mechanisms underlying Mg's influence on inflammation and angiogenesis.
Main Methods:
- Cultured microvascular 1G11 cells were exposed to different Mg concentrations.
- Assays were performed to measure cell growth, migration, and inflammatory marker synthesis.
- Key inflammatory mediators like interleukin-1α, interleukin-6, nitric oxide, and VCAM were quantified.
Main Results:
- Low Mg concentrations inhibited endothelial cell growth and migration.
- Low Mg increased the synthesis of inflammatory markers: interleukin-1α, interleukin-6, nitric oxide, and VCAM.
- High Mg concentrations stimulated endothelial cell proliferation and migration.
- High Mg sensitized cells to migratory signals, promoting angiogenesis.
Conclusions:
- Magnesium plays a direct role in modulating microvascular endothelial cell functions.
- Mg concentration influences both inflammatory responses and angiogenic processes.
- These findings provide a molecular basis for the in vivo association between Mg, angiogenesis, and inflammation.
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