Arginine Vasopressin-Containing Neurons of the Suprachiasmatic Nucleus Project to CSF

被引:15
作者
Taub, Alana [1 ]
Carbajal, Yvette [2 ]
Rimu, Kania [2 ]
Holt, Rebecca [2 ]
Yao, Yifan [1 ]
Hernandez, Amanda L. [1 ]
LeSauter, Joseph [2 ]
Silver, Rae [1 ,2 ,3 ]
机构
[1] Columbia Univ, Dept Psychol, New York, NY 10027 USA
[2] Barnard Coll, Dept Neurosci, New York, NY 10027 USA
[3] Columbia Univ, Grad Fac, Dept Pathol & Cell Biol, Med Sch, New York, NY 10032 USA
基金
美国国家科学基金会;
关键词
CSF; suprachiasmatic; vasopressin; EFFERENT PROJECTIONS; CEREBROSPINAL-FLUID; CIRCADIAN-RHYTHMS; GOLDEN-HAMSTER; RAT; BRAIN; CELL; MOUSE; OUTPUT; IDENTIFICATION;
D O I
10.1523/ENEURO.0363-20.2021
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Arginine vasopressin (AVP) expressing neurons form the major population in the brain's circadian clock located in the hypothalamic suprachiasmatic nucleus (SCN). They participate in inter-neuronal coupling and provide an output signal for synchronizing daily rhythms. AVP is present at high concentrations in the cerebrospinal fluid (CSF) and fluctuates on a circadian timescale. While it is assumed that rhythms in CSF AVP are of SCN origin, a route of communication between these compartments has not been delineated. Using immunochemistry (ICC) and cell filling techniques, we determine the morphology and location of AVP neurons in mouse and delineate their axonal and dendritic processes. Cholera toxin beta subunit (CT beta) tracer injected into the lateral ventricle tests whether AVP neurons communicate with CSF. Most importantly, the results indicate that AVP neurons lie in close proximity to the third ventricle, and their processes cross the ventricular wall into the CSF. We also report that contrary to widely held assumptions, AVP neurons do not fully delineate the SCN borders as PER2 expression extends beyond the AVP region. Also, AVP neurons form a rostral prong originating in the SCN medial-most and ventral-most aspect. AVP is lacking in the mid-dorsal shell but does occur at the base of the SCN just above the optic tract. Finally, neurons of the rostral SCN are smaller than those lying caudally. These findings extend our understanding of AVP signaling potential, demonstrate the heterogeneity of AVP neurons, and highlight limits in using this peptide to delineate the mouse SCN.
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页数:15
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