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The nuclear receptor Hr46/Hr3 is required in the blood brain barrier of mature males for courtship

The blood brain barrier (BBB) forms a stringent barrier that protects the brain from components in the circulation that could interfere with neuronal function. At the same time, the BBB enables selective transport of critical nutrients and other chemicals to the brain. Beyond these functions, anothe...

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Autores principales: Lama, Chamala, Love, Cameron R., Le, Hoa Nhu, Waqar, Marium, Reeve, Joseph L., Lama, Jyoti, Dauwalder, Brigitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8815886/
https://www.ncbi.nlm.nih.gov/pubmed/35077443
http://dx.doi.org/10.1371/journal.pgen.1009519
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author Lama, Chamala
Love, Cameron R.
Le, Hoa Nhu
Waqar, Marium
Reeve, Joseph L.
Lama, Jyoti
Dauwalder, Brigitte
author_facet Lama, Chamala
Love, Cameron R.
Le, Hoa Nhu
Waqar, Marium
Reeve, Joseph L.
Lama, Jyoti
Dauwalder, Brigitte
author_sort Lama, Chamala
collection PubMed
description The blood brain barrier (BBB) forms a stringent barrier that protects the brain from components in the circulation that could interfere with neuronal function. At the same time, the BBB enables selective transport of critical nutrients and other chemicals to the brain. Beyond these functions, another recently recognized function is even less characterized, specifically the role of the BBB in modulating behavior by affecting neuronal function in a sex-dependent manner. Notably, signaling in the adult Drosophila BBB is required for normal male courtship behavior. Courtship regulation also relies on male-specific molecules in the BBB. Our previous studies have demonstrated that adult feminization of these cells in males significantly lowered courtship. Here, we conducted microarray analysis of BBB cells isolated from males and females. Findings revealed that these cells contain male- and female-enriched transcripts, respectively. Among these transcripts, nuclear receptor Hr46/Hr3 was identified as a male-enriched BBB transcript. Hr46/Hr3 is best known for its essential roles in the ecdysone response during development and metamorphosis. In this study, we demonstrate that Hr46/Hr3 is specifically required in the BBB cells for courtship behavior in mature males. The protein is localized in the nuclei of sub-perineurial glial cells (SPG), indicating that it might act as a transcriptional regulator. These data provide a catalogue of sexually dimorphic BBB transcripts and demonstrate a physiological adult role for the nuclear receptor Hr46/Hr3 in the regulation of male courtship, a novel function that is independent of its developmental role.
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spelling pubmed-88158862022-02-05 The nuclear receptor Hr46/Hr3 is required in the blood brain barrier of mature males for courtship Lama, Chamala Love, Cameron R. Le, Hoa Nhu Waqar, Marium Reeve, Joseph L. Lama, Jyoti Dauwalder, Brigitte PLoS Genet Research Article The blood brain barrier (BBB) forms a stringent barrier that protects the brain from components in the circulation that could interfere with neuronal function. At the same time, the BBB enables selective transport of critical nutrients and other chemicals to the brain. Beyond these functions, another recently recognized function is even less characterized, specifically the role of the BBB in modulating behavior by affecting neuronal function in a sex-dependent manner. Notably, signaling in the adult Drosophila BBB is required for normal male courtship behavior. Courtship regulation also relies on male-specific molecules in the BBB. Our previous studies have demonstrated that adult feminization of these cells in males significantly lowered courtship. Here, we conducted microarray analysis of BBB cells isolated from males and females. Findings revealed that these cells contain male- and female-enriched transcripts, respectively. Among these transcripts, nuclear receptor Hr46/Hr3 was identified as a male-enriched BBB transcript. Hr46/Hr3 is best known for its essential roles in the ecdysone response during development and metamorphosis. In this study, we demonstrate that Hr46/Hr3 is specifically required in the BBB cells for courtship behavior in mature males. The protein is localized in the nuclei of sub-perineurial glial cells (SPG), indicating that it might act as a transcriptional regulator. These data provide a catalogue of sexually dimorphic BBB transcripts and demonstrate a physiological adult role for the nuclear receptor Hr46/Hr3 in the regulation of male courtship, a novel function that is independent of its developmental role. Public Library of Science 2022-01-25 /pmc/articles/PMC8815886/ /pubmed/35077443 http://dx.doi.org/10.1371/journal.pgen.1009519 Text en © 2022 Lama et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lama, Chamala
Love, Cameron R.
Le, Hoa Nhu
Waqar, Marium
Reeve, Joseph L.
Lama, Jyoti
Dauwalder, Brigitte
The nuclear receptor Hr46/Hr3 is required in the blood brain barrier of mature males for courtship
title The nuclear receptor Hr46/Hr3 is required in the blood brain barrier of mature males for courtship
title_full The nuclear receptor Hr46/Hr3 is required in the blood brain barrier of mature males for courtship
title_fullStr The nuclear receptor Hr46/Hr3 is required in the blood brain barrier of mature males for courtship
title_full_unstemmed The nuclear receptor Hr46/Hr3 is required in the blood brain barrier of mature males for courtship
title_short The nuclear receptor Hr46/Hr3 is required in the blood brain barrier of mature males for courtship
title_sort nuclear receptor hr46/hr3 is required in the blood brain barrier of mature males for courtship
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8815886/
https://www.ncbi.nlm.nih.gov/pubmed/35077443
http://dx.doi.org/10.1371/journal.pgen.1009519
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