Dynamic Changes in Spontaneous Intracellular Free Calcium Oscillations and Their Relationship to Prolactin Gene Expression in Single, Primary Mammotropes
Cytosolic calcium plays a critical role in the control of a number of genes, including that of the pituitary hormone PRL. Cells that secrete this hormone, termed mammotropes, display spontaneous oscillations of intracellular free calcium ([Ca2+]i) that are positively correlated to PRL release. Howev...
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Veröffentlicht in: | Molecular endocrinology (Baltimore, Md.) Md.), 1998-01, Vol.12 (1), p.87-95 |
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Zusammenfassung: | Cytosolic calcium plays a critical role in the
control of a number of genes, including that of the pituitary hormone
PRL. Cells that secrete this hormone, termed mammotropes, display
spontaneous oscillations of intracellular free calcium
([Ca2+]i) that are
positively correlated to PRL release. However, the precise contribution
of calcium signaling to the expression of any gene including PRL has
remained obscure owing to the requirement for and lack of a strategy
for monitoring both of these dynamic variables (gene expression and[
Ca2+]i oscillations)
in the same living cell. In the present study, we overcame this
technical limitation by making real-time measurements of PRL gene
expression in transfected, primary rat mammotropes previously subjected
to [Ca2+]i
determinations by digital imaging fluorescence microscopy of fura-2.
Our results showed that the majority of mammotropes (75%) exhibited
distinct oscillatory behaviors that could be subgrouped on the basis of
frequency/amplitude of[
Ca2+]i changes,
whereas the remainder (25%) were quiescent (nonoscillatory).
Interestingly, most mammotropes displayed spontaneous transitions
between oscillatory and quiescent states over the course of several
hours. As a consequence of this oscillatory plasticity, there was not a
positive correlation between[
Ca2+]i dynamics and
gene expression at any point in time, as would be predicted by studies
with entire populations of cells. Instead, the relationship was
distinctly inverse, suggesting that dynamic changes in PRL gene
expression may be regulated by temporally dissociated transitions
between quiescent and oscillatory states. |
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ISSN: | 0888-8809 1944-9917 |
DOI: | 10.1210/mend.12.1.0055 |