Key result
17beta-estradiol (E2) had no gross effect on the ependymal pattern of Angpt1 immunoreactivity or cerebral Angpt1 protein content in vivo in rat brains.
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The study maps the localization of Angpt1 and Tie2 in the rat brain, suggesting a functional ligand-receptor interaction between cerebrospinal fluid and vascular compartments that is not modulated by estradiol.
Angiopoietin-1 (Angpt1; previously Ang-1) participates in vascular maintenance and remodeling. In the current study, we investigated the distribution of Angpt1 protein in rat brain. We detected Angpt1 immunoreactivity (IR) in cerebral blood vessels, cuboidal ependyma, and tanycytes, which are specialized hypothalamic bipolar ependymal cells. We also evaluated patterns of IR of endothelium-specific receptor tyrosine kinase 2 (Tie2, the receptor for Angpt1). Tie2 IR was present in Angpt1-immunoreactive cuboidal ependyma in a membranous pattern, suggesting an autocrine or paracrine role for Angpt1-Tie2. Tie2 IR was also associated with peri-ependymal blood vessels, some of which were contacted by tips of Angpt1-immunoreactive tanycyte processes, implying a potential functional ligand-receptor interaction mediating communication between the cerebrospinal fluid and vascular compartments. Because we previously found that cerebral Angpt1 expression was modulated by 17beta-estradiol (E2), and because some tanycyte functions are modulated by E2, we tested the hypothesis that E2 affects ependymal and tanycyte Angpt1 expression in vivo. No gross E2 effect on the ependymal pattern of Angpt1 IR or cerebral Angpt1 protein content was observed.
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Horton et al. (2009) studied this question. 17beta-estradiol (E2) was evaluated on Ependymal pattern of Angpt1 immunoreactivity or cerebral Angpt1 protein content. 17beta-estradiol (E2) had no gross effect on the ependymal pattern of Angpt1 immunoreactivity or cerebral Angpt1 protein content in vivo in rat brains.
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