4.6 Article

Anatomical Organization of the Rat Subfornical Organ

Journal

FRONTIERS IN CELLULAR NEUROSCIENCE
Volume 15, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fncel.2021.691711

Keywords

glia cells; tanycytes; osmoregulation; angiotensin II; fenestrated blood capillary; blood-brain barrier

Categories

Funding

  1. Canadian Institutes of Health Research Project Grant [PJT-153009, RGPIN/05184-2017]
  2. Council of Canada [RGPIN-201705184]
  3. Heart and Stroke Foundation of Canada National New Investigator Award
  4. Healthy Brains for Healthy Lives Ph.D. fellowship award

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The subfornical organ (SFO) is a sensory circumventricular organ located along the anterodorsal wall of the third ventricle. SFO lacks a complete blood-brain barrier (BBB), and thus peripherally-circulating factors can penetrate the SFO parenchyma. The anatomical organization of the rat SFO reveals unique populations of non-neuronal cells, different types of vasculature, and distinct neuronal responses to stimuli like angiotensin II or hypertonic NaCl.
The subfornical organ (SFO) is a sensory circumventricular organ located along the anterodorsal wall of the third ventricle. SFO lacks a complete blood-brain barrier (BBB), and thus peripherally-circulating factors can penetrate the SFO parenchyma. These signals are detected by local neurons providing the brain with information from the periphery to mediate central responses to humoral signals and physiological stressors. Circumventricular organs are characterized by the presence of unique populations of non-neuronal cells, such as tanycytes and fenestrated endothelium. However, how these populations are organized within the SFO is not well understood. In this study, we used histological techniques to analyze the anatomical organization of the rat SFO and examined the distribution of neurons, fenestrated and non-fenestrated vasculature, tanycytes, ependymocytes, glia cells, and pericytes within its confines. Our data show that the shell of SFO contains non-fenestrated vasculature, while fenestrated capillaries are restricted to the medial-posterior core region of the SFO and associated with a higher BBB permeability. In contrast to non-fenestrated vessels, fenestrated capillaries are encased in a scaffold created by pericytes and embedded in a network of tanycytic processes. Analysis of c-Fos expression following systemic injections of angiotensin II or hypertonic NaCl reveals distinct neuronal populations responding to these stimuli. Hypertonic NaCl activates similar to 13% of SFO neurons located in the shell. Angiotensin II-sensitive neurons represent similar to 35% of SFO neurons and their location varies between sexes. Our study provides a comprehensive description of the organization of diverse cellular elements within the SFO, facilitating future investigations in this important brain area.

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