Abstract

Corticotropin-releasing hormone (CRH)-containing neurons in the paraventricular nucleus of the hypothalamus (PVN) initiate and control neuroendocrine responses to psychogenic and physical stress. Investigations into the physiology of CRH neurons, however, have been hampered by the lack of tools for adequately targeting or visualizing this cell population. Here we characterize CRH neurons in the PVN of mice that express tdTomato fluorophore, generated by crosses of recently developed Crh-IRES-Cre driver and Ai14 Cre-reporter mouse strains. tdTomato containing PVN neurons in Crh-IRES-Cre;Ai14 mice are readily visualized without secondary-detection methods. These neurons are predominantly neuroendocrine and abundantly express CRH protein, but not other PVN phenotypic neuropeptides. After an acute stress, a large majority of tdTomato cells express neuronal activation marker c-Fos. Finally, tdTomato PVN neurons exhibit homogenous intrinsic biophysical and synaptic properties, and can be optogenetically manipulated by viral Cre-driven expression of channelrhodopsin. These observations highlight basic cell-type characteristics of CRH neurons in a mutant mouse, providing validation for its future use in probing neurophysiology of endocrine stress responses.

Highlights

  • Real and perceived threats to survival engage an evolutionarily conserved endocrine stress response

  • At the head of the hypothalamic-pituitary-adrenal axis (HPA) axis is a cluster of parvocellular neuroendocrine cells (PNCs) in the paraventricular nucleus of the hypothalamus (PVN) [2]

  • We found that simple crosses of these founders with Ai14 Cre-reporter mice [14] generated Crh-IRES-Cre;Ai14 progeny with robust PVN expression of red tdTomato fluorescence. tdTomato expressing PVN neurons were and directly visible in live and fixed tissue

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Summary

Introduction

Real and perceived threats to survival engage an evolutionarily conserved endocrine stress response Part of this response, mediated by a hypothalamic-pituitary-adrenal axis (HPA), culminates in the release of glucocorticoid hormones in to the blood, promoting critical body-wide adaptive changes [1]. The most widely studied of these is corticotropin releasing hormone (CRH) or factor (CRF), a 41 amino-acid peptide [3,4]. Despite their critical roles in HPA axis function, adequate and robust tools for visualizing and targeting the neurons that manufacture and release CRH have lagged behind those for other cell types. The paucity of accumulated CRH peptide in cell bodies has necessitated the use of additional tools such as colchicine [5] for identifying cells, but this approach makes physiological experiments unreliable; in addition, experience dependent shifts in the expression of hypothalamic peptides [6,7]

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