Endoplasmic Reticulum and Mitochondrial Calcium Handling Dynamically Shape Slow Afterhyperpolarizations in Vasopressin Magnocellular Neurons.
Matthew K KirchnerFerdinand AlthammerElba Campos-LiraJuliana MontanezJavier E SternPublished in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2024)
Many neurons including vasopressin (VP) magnocellular neurosecretory cells (MNCs) of the hypothalamic supraoptic nucleus (SON) generate afterhyperpolarizations (AHPs) during spiking to slow firing, a phenomenon known as spike frequency adaptation. The AHP is underlain by Ca 2+ -activated K + currents, and while slow component (sAHP) features are well described, its mechanism remains poorly understood. Previous work demonstrated that Ca 2+ influx through N-type Ca 2+ channels is a primary source of sAHP activation in SON oxytocin neurons, but no obvious channel coupling was described for VP neurons. Given this, we tested the possibility of an intracellular source of sAHP activation, namely, the Ca 2+ -handling organelles endoplasmic reticulum (ER) and mitochondria in male and female Wistar rats. We demonstrate that ER Ca 2+ depletion greatly inhibits sAHPs without a corresponding decrease in Ca 2+ signal. Caffeine sensitized AHP activation by Ca 2+ In contrast to ER, disabling mitochondria with CCCP or blocking mitochondria Ca 2+ uniporters (MCUs) enhanced sAHP amplitude and duration, implicating mitochondria as a vital buffer for sAHP-activating Ca 2+ Block of mitochondria Na + -dependent Ca 2+ release via triphenylphosphonium (TPP + ) failed to affect sAHPs, indicating that mitochondria Ca 2+ does not contribute to sAHP activation. Together, our results suggests that ER Ca 2+ -induced Ca 2+ release activates sAHPs and mitochondria shape the spatiotemporal trajectory of the sAHP via Ca 2+ buffering in VP neurons. Overall, this implicates organelle Ca 2+ , and specifically ER-mitochondria-associated membrane contacts, as an important site of Ca 2+ microdomain activity that regulates sAHP signaling pathways. Thus, this site plays a major role in influencing VP firing activity and systemic hormonal release.