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Published on: February 20, 2019
Interleukin-1 suppresses mesangial cell growth via inhibition of Ca2+ entry
Insights
Interleukin-1 (IL-1) inhibits rat mesangial cell growth by blocking calcium (Ca2+) entry. This suggests IL-1 impacts cell proliferation through calcium signaling pathways.
Area of Science:
- Cell Biology
- Renal Physiology
- Immunology
Background:
- Interleukin-1 (IL-1) is a key cytokine involved in inflammation and cellular processes.
- Calcium (Ca2+) homeostasis is crucial for regulating cell growth and function.
- Rat mesangial cells are important components of the renal glomerulus, influencing kidney function.
Purpose of the Study:
- To investigate the effects of IL-1 on the proliferation and calcium handling of cultured rat mesangial cells.
- To determine the role of calcium influx in IL-1-mediated effects on mesangial cells.
Main Methods:
- Cell culture of rat mesangial cells.
- Measurement of DNA synthesis using [3H]thymidine uptake.
- Assessment of calcium (45Ca2+) uptake.
- Treatment with IL-1 and nicardipine (a calcium channel antagonist).
Main Results:
- IL-1 significantly inhibited DNA synthesis in mesangial cells.
- Nicardipine also significantly inhibited DNA synthesis.
- Both IL-1 and nicardipine significantly reduced 45Ca2+ uptake by mesangial cells.
- IL-1's inhibitory effect on cell growth correlated with reduced calcium influx.
Conclusions:
- IL-1 suppresses the growth of rat mesangial cells.
- This suppression appears to be mediated by the inhibition of extracellular calcium entry into the cytosol.
- Calcium signaling plays a critical role in mediating the effects of IL-1 on mesangial cell proliferation.
Abstract:
We have investigated the effect of interleukin-1 (IL-1) on the cell growth and Ca2+ homeostasis of rat mesangial cells in culture. DNA synthesis measured by [3H]thymidine uptake by mesangial cells was significantly inhibited by IL-1 (10 U/ml) and the calcium channel antagonist nicardipine (5 x 10(-6) M). 45Ca2+ uptake by mesangial cells was also significantly inhibited by IL-1 and nicardipine. The above observations support the premise that IL-1 suppresses the growth of mesangial cells via inhibition of extracellular Ca2+ entry to the cytosol.
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