Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVN
Hypothalamic oxytocinergic magnocellular neurons have a fascinating ability to release peptide from both their axon terminals and from their dendrites. Existing data indicates that the relationship between somatic activity and dendritic release is not constant, but the mechanisms through which this...
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doaj-19dfdf9a26634505adf3a81dff24a0a32021-09-22T17:02:37ZengeLife Sciences Publications LtdeLife2050-084X2021-07-011010.7554/eLife.63486Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVNWanhui Sheng0https://orcid.org/0000-0001-9357-0771Scott W Harden1https://orcid.org/0000-0002-0757-1979Yalun Tan2Eric G Krause3https://orcid.org/0000-0002-2718-3113Charles J Frazier4https://orcid.org/0000-0003-3550-4789Department of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, United StatesDepartment of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, United StatesDepartment of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, United States; Department of Anesthesiology, School of Medicine, Stanford University, Stanford, United StatesDepartment of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, United States; Center for Integrative Cardiovascular and Metabolic Diseases, University of Florida, Gainesville, United States; Evelyn F. and William L. McKnight Brain Institute, University of Florida, Gainesville, United StatesDepartment of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, United States; Center for Integrative Cardiovascular and Metabolic Diseases, University of Florida, Gainesville, United StatesHypothalamic oxytocinergic magnocellular neurons have a fascinating ability to release peptide from both their axon terminals and from their dendrites. Existing data indicates that the relationship between somatic activity and dendritic release is not constant, but the mechanisms through which this relationship can be modulated are not completely understood. Here, we use a combination of electrical and optical recording techniques to quantify activity-induced calcium influx in proximal vs. distal dendrites of oxytocinergic magnocellular neurons located in the paraventricular nucleus of the hypothalamus (OT-MCNs). Results reveal that the dendrites of OT-MCNs are weak conductors of somatic voltage changes; however, activity-induced dendritic calcium influx can be robustly regulated by both osmosensitive and non-osmosensitive ion channels located along the dendritic membrane. Overall, this study reveals that dendritic conductivity is a dynamic and endogenously regulated feature of OT-MCNs that is likely to have substantial functional impact on central oxytocin release.https://elifesciences.org/articles/63486oxytocinhypothalamusmagnocellular neuronPVNdendriteelectrophysiology |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wanhui Sheng Scott W Harden Yalun Tan Eric G Krause Charles J Frazier |
spellingShingle |
Wanhui Sheng Scott W Harden Yalun Tan Eric G Krause Charles J Frazier Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVN eLife oxytocin hypothalamus magnocellular neuron PVN dendrite electrophysiology |
author_facet |
Wanhui Sheng Scott W Harden Yalun Tan Eric G Krause Charles J Frazier |
author_sort |
Wanhui Sheng |
title |
Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVN |
title_short |
Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVN |
title_full |
Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVN |
title_fullStr |
Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVN |
title_full_unstemmed |
Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVN |
title_sort |
dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse pvn |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2021-07-01 |
description |
Hypothalamic oxytocinergic magnocellular neurons have a fascinating ability to release peptide from both their axon terminals and from their dendrites. Existing data indicates that the relationship between somatic activity and dendritic release is not constant, but the mechanisms through which this relationship can be modulated are not completely understood. Here, we use a combination of electrical and optical recording techniques to quantify activity-induced calcium influx in proximal vs. distal dendrites of oxytocinergic magnocellular neurons located in the paraventricular nucleus of the hypothalamus (OT-MCNs). Results reveal that the dendrites of OT-MCNs are weak conductors of somatic voltage changes; however, activity-induced dendritic calcium influx can be robustly regulated by both osmosensitive and non-osmosensitive ion channels located along the dendritic membrane. Overall, this study reveals that dendritic conductivity is a dynamic and endogenously regulated feature of OT-MCNs that is likely to have substantial functional impact on central oxytocin release. |
topic |
oxytocin hypothalamus magnocellular neuron PVN dendrite electrophysiology |
url |
https://elifesciences.org/articles/63486 |
work_keys_str_mv |
AT wanhuisheng dendriticosmosensorsmodulateactivityinducedcalciuminfluxinoxytocinergicmagnocellularneuronsofthemousepvn AT scottwharden dendriticosmosensorsmodulateactivityinducedcalciuminfluxinoxytocinergicmagnocellularneuronsofthemousepvn AT yaluntan dendriticosmosensorsmodulateactivityinducedcalciuminfluxinoxytocinergicmagnocellularneuronsofthemousepvn AT ericgkrause dendriticosmosensorsmodulateactivityinducedcalciuminfluxinoxytocinergicmagnocellularneuronsofthemousepvn AT charlesjfrazier dendriticosmosensorsmodulateactivityinducedcalciuminfluxinoxytocinergicmagnocellularneuronsofthemousepvn |
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1717371289592659968 |