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Stereotaxic Surgical Approach to Microinject the Caudal Brainstem and Upper Cervical Spinal Cord via the Cisterna Magna in Mice
Published on: January 21, 2022
The arcuate nucleus as a circumventricular organ in the mouse
1Institut National de la Santé et de la Recherche Médicale, Institut François Magendie, Bordeaux, France. philippe.ciofi@inserm.fr
Abstract:
The present study searched for morphological correlates of the permeability of the ventromedial arcuate nucleus of the mouse to blood-borne proteins. First, we determined that highly permeable microvessels are detected in the ventromedial arcuate nucleus using a rat monoclonal antibody to a mouse-specific endothelial phenotype (clone MECA32) recently recognized as a marker of endothelial fenestral diaphragms and previously shown to label circumventricular organs. Second, in the mild conditions of tissue fixation mandatory for use of MECA32, we observed that after a rapid vascular flush with saline, endogenous immunoglobulins are especially retained in circumventricular organs and ventromedial arcuate nucleus. The ventromedial arcuate nucleus thus shares features in common with classical circumventricular organs.
Insights
The ventromedial arcuate nucleus in mice has highly permeable microvessels, similar to circumventricular organs. This suggests it allows greater passage of blood-borne proteins and molecules.
Area of Science:
- Neuroscience
- Vascular Biology
- Cell Biology
Background:
- The ventromedial arcuate nucleus (VMH) plays a crucial role in regulating physiological functions.
- Understanding the blood-brain barrier (BBB) permeability in specific brain regions is vital for drug delivery and understanding neurological disorders.
- Circumventricular organs (CVOs) are known for their unique vascular permeability.
Purpose of the Study:
- To investigate the morphological basis for the permeability of the mouse ventromedial arcuate nucleus to blood-borne proteins.
- To determine if the ventromedial arcuate nucleus shares vascular characteristics with known circumventricular organs.
Main Methods:
- Utilized a rat monoclonal antibody (clone MECA32), a marker for endothelial fenestral diaphragms, to identify permeable microvessels.
- Employed mild tissue fixation techniques compatible with MECA32 antibody.
- Performed rapid vascular flushing with saline followed by immunodetection of endogenous immunoglobulins.
Main Results:
- Highly permeable microvessels, identified by MECA32, were detected in the ventromedial arcuate nucleus.
- Endogenous immunoglobulins were retained in the ventromedial arcuate nucleus and CVOs under mild fixation conditions.
- These findings indicate shared vascular permeability features between the ventromedial arcuate nucleus and CVOs.
Conclusions:
- The ventromedial arcuate nucleus exhibits high microvessel permeability, comparable to circumventricular organs.
- Morphological evidence supports the notion that the ventromedial arcuate nucleus allows significant passage of blood-borne substances.
- This increased permeability may influence the nucleus's function in integrating systemic signals.
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