Literature DB >> 28840477

A Working Module for the Neurovascular Unit in the Sexually Dimorphic Nucleus of the Preoptic Area.

Zhen He1, Li Cui2, Sherry A Ferguson3, Merle G Paule3.   

Abstract

The neurovascular unit (NVU) can be conceptualized as a functional entity consisting of neurons, astrocytes, pericytes, and endothelial and smooth muscle cells that operate in concert to affect blood flow to a very circumscribed area. Although we are currently in a "golden era" of bioengineering, there are, as yet, no living NVUs-on-a-chip modules available and the development of a neural chip that would mimic NVUs is a seemingly lofty goal. The sexually dimorphic nucleus of the preoptic area (SDN-POA) is a tiny brain structure (between 0.001~0.007 mm3 in rats) with an assessable biological function (i.e., male sexual behavior). The present effort was undertaken to determine whether there are identifiable NVUs in the SDN-POA by assessing its vasculature relative to its known neural components. First, a thorough and systematic review of thousands of histologic and immunofluorescent images from 201 weanling and adult rats was undertaken to define the characteristics of the vessels supplying the SDN-POA: its primary supply artery/arteriole and capillaries are physically inseparable from their neural elements. A subsequent immunofluorescent study targeting α-smooth muscle actin confirmed the identity of an artery/arteriole supplying the SDN-POA. In reality, the predominant components of the SDN-POA are calbindin D28k-positive neurons that are comingled with tyrosine hydroxylase-positive projections. Finally, a schematic of an SDN-POA NVU is proposed as a working model of the basic building block of the CNS. Such modules could serve the study of neurovascular mechanisms and potentially inform the development of next generation bioengineered neural transplants, i.e., the construct of an NVU neural chip.

Entities:  

Keywords:  Bioengineered neural chip; Capillaries; Neurovascular unit; Primary supply artery; Sexually dimorphic nucleus; α-Smooth muscle actin

Mesh:

Year:  2018        PMID: 28840477     DOI: 10.1007/s12035-017-0729-6

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN: 0893-7648            Impact factor:   5.590


  30 in total

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4.  Perinatal exposures to rotating magnetic fields 'demasculinize' neuronal density in the medial preoptic nucleus of male rats.

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Authors:  Z He; T Yamawaki; S Yang; A L Day; J W Simpkins; H Naritomi
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6.  Pre- and postnatal bisphenol A treatment does not alter the number of tyrosine hydroxylase-positive cells in the anteroventral periventricular nucleus (AVPV) of weanling male and female rats.

Authors:  Sherry A Ferguson; Merle G Paule; Zhen He
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Authors:  Alicia Garcia-Falgueras; Dick F Swaab
Journal:  Brain       Date:  2008-11-02       Impact factor: 13.501

8.  A difference in hypothalamic structure between heterosexual and homosexual men.

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10.  Administration of S-nitrosoglutathione after traumatic brain injury protects the neurovascular unit and reduces secondary injury in a rat model of controlled cortical impact.

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