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Localization of Ca++-containing antimonate precipitates during mitosis
The Journal of Cell Biology
|August 1, 1980
Summary
This study visualizes intracellular calcium (Ca++) during plant cell division in Marsilea vestita and Hordeum vulgare. Calcium is found in various organelles, particularly the endoplasmic reticulum (ER), suggesting its role in regulating cell division processes.
Area of Science:
- Plant cell biology
- Cellular and molecular biology
- Biochemistry
Background:
- Calcium ions (Ca++) play crucial roles in cellular processes, including cell division.
- Understanding the localization of intracellular calcium is vital for elucidating its regulatory functions.
- Previous studies have suggested calcium's involvement in mitosis and cytokinesis, but precise localization remains to be fully detailed.
Purpose of the Study:
- To localize intracellular bound calcium (Ca++) during mitosis and cytokinesis in plant cells.
- To investigate the association of calcium with specific organelles during cell division.
- To explore the potential role of calcium in regulating the mitotic apparatus.
Main Methods:
- In situ precipitation using potassium antimonate.
- Electron microscopy for visualization of antimonate deposits.
- Solubility tests (water, EDTA, EGTA) to identify the precipitated cation as Ca++.
Main Results:
- Antimonate deposits, indicating Ca++, were found in the endoplasmic reticulum (ER), vacuoles, euchromatin/nucleoplasm, and mitochondria in both Marsilea vestita and Hordeum vulgare.
- Mitochondria showed higher Ca++ density in Marsilea than in Hordeum.
- Smooth ER surrounding the mitotic spindle contained significant Ca++ deposits, suggesting a role in regulating the mitotic apparatus.
Conclusions:
- Intracellular calcium is localized in various organelles throughout mitosis and cytokinesis in the studied plant species.
- The endoplasmic reticulum (ER), especially the smooth ER associated with the mitotic spindle, is a significant site for calcium localization.
- The Ca++-binding capacity of the ER suggests its involvement in regulating free Ca++ levels critical for Ca++-sensitive processes during cell division.