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Adenosine triphosphate--dependent calcium uptake by rat submaxillary gland microsomes
The Journal of General Physiology
|September 1, 1971
Summary
Rat submaxillary gland microsomes utilize adenosine triphosphate (ATP) for calcium uptake, essential for cellular function. This ATP-dependent calcium transport is crucial for regulating intracellular calcium levels after secretion.
Area of Science:
- Biochemistry
- Cell Biology
- Physiology
Background:
- Microsomes are membrane-bound vesicles derived from cellular endomembranes.
- Calcium ions play critical roles in various cellular processes, including muscle contraction and signal transduction.
- Submaxillary glands are exocrine glands involved in saliva production.
Purpose of the Study:
- To investigate the mechanism of calcium uptake by rat submaxillary gland microsomes.
- To determine the role of adenosine triphosphate (ATP) in this calcium transport process.
- To compare calcium uptake in salivary gland microsomes with that in muscle tissues.
Main Methods:
- Isolation of microsomes from rat submaxillary glands.
- Measurement of calcium uptake in vitro under various conditions.
- Assay of ATP-dependent calcium transport in the presence of cofactors like magnesium and oxalate.
Main Results:
- Rat submaxillary gland microsomes exhibit calcium uptake from the surrounding media.
- Adenosine triphosphate (ATP) significantly enhances calcium uptake, an effect dependent on temperature (not observed at 0°C) and magnesium ions.
- Oxalate and inorganic phosphate further potentiate ATP-dependent calcium uptake, with oxalate showing a greater effect.
- The total calcium content in microsomes is comparable to that reported for skeletal and cardiac muscles, although the uptake rate is slower in salivary gland microsomes.
Conclusions:
- The study demonstrates an ATP-dependent calcium uptake mechanism in rat submaxillary gland microsomes.
- This process is likely mediated by a calcium pump requiring ATP, magnesium, and potentially influenced by oxalate and phosphate.
- The findings suggest that ATP-dependent calcium sequestration may contribute to the regulation of intracellular free calcium levels, facilitating the return of secretory cells to a resting state.