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Hiat1 as a new transporter involved in ammonia regulation
The orphan transporter hippocampus-abundant transcript 1 (Hiat1) was first identified in the mammalian brain. Its specific substrate specificity, however, has not been investigated to date. Here, we identified and analyzed Hiat1 in a crustacean, the green crab Carcinus maenas. Our phylogenetic analy...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023664/ https://www.ncbi.nlm.nih.gov/pubmed/36932112 http://dx.doi.org/10.1038/s41598-023-31503-0 |
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author | Fehsenfeld, Sandra Quijada-Rodriguez, Alex R. Zhouyao, Haonan Durant, Andrea C. Donini, Andrew Sachs, Maria Eck, Peter Weihrauch, Dirk |
author_facet | Fehsenfeld, Sandra Quijada-Rodriguez, Alex R. Zhouyao, Haonan Durant, Andrea C. Donini, Andrew Sachs, Maria Eck, Peter Weihrauch, Dirk |
author_sort | Fehsenfeld, Sandra |
collection | PubMed |
description | The orphan transporter hippocampus-abundant transcript 1 (Hiat1) was first identified in the mammalian brain. Its specific substrate specificity, however, has not been investigated to date. Here, we identified and analyzed Hiat1 in a crustacean, the green crab Carcinus maenas. Our phylogenetic analysis showed that Hiat1 protein is conserved at a considerable level between mammals and this invertebrate (ca. 78% identical and conserved amino acids). Functional expression of Carcinus maenas Hiat1 in Xenopus laevis oocytes demonstrated the capability to transport ammonia (likely NH(4)(+)) in a sodium-dependent manner. Furthermore, applying quantitative polymerase chain reaction, our results indicated a physiological role for Carcinus maenas Hiat1 in ammonia homeostasis, as mRNA abundance increased in posterior gills in response to elevated circulating hemolymph ammonia upon exposure to high environmental ammonia. Its ubiquitous mRNA expression pattern also suggests an essential role in general cellular detoxification of ammonia. Overall, our results introduce a new ubiquitously expressed ammonia transporter, consequently demanding revision of our understanding of ammonia handling in key model systems from mammalian kidneys to crustacean and fish gills. |
format | Online Article Text |
id | pubmed-10023664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100236642023-03-19 Hiat1 as a new transporter involved in ammonia regulation Fehsenfeld, Sandra Quijada-Rodriguez, Alex R. Zhouyao, Haonan Durant, Andrea C. Donini, Andrew Sachs, Maria Eck, Peter Weihrauch, Dirk Sci Rep Article The orphan transporter hippocampus-abundant transcript 1 (Hiat1) was first identified in the mammalian brain. Its specific substrate specificity, however, has not been investigated to date. Here, we identified and analyzed Hiat1 in a crustacean, the green crab Carcinus maenas. Our phylogenetic analysis showed that Hiat1 protein is conserved at a considerable level between mammals and this invertebrate (ca. 78% identical and conserved amino acids). Functional expression of Carcinus maenas Hiat1 in Xenopus laevis oocytes demonstrated the capability to transport ammonia (likely NH(4)(+)) in a sodium-dependent manner. Furthermore, applying quantitative polymerase chain reaction, our results indicated a physiological role for Carcinus maenas Hiat1 in ammonia homeostasis, as mRNA abundance increased in posterior gills in response to elevated circulating hemolymph ammonia upon exposure to high environmental ammonia. Its ubiquitous mRNA expression pattern also suggests an essential role in general cellular detoxification of ammonia. Overall, our results introduce a new ubiquitously expressed ammonia transporter, consequently demanding revision of our understanding of ammonia handling in key model systems from mammalian kidneys to crustacean and fish gills. Nature Publishing Group UK 2023-03-17 /pmc/articles/PMC10023664/ /pubmed/36932112 http://dx.doi.org/10.1038/s41598-023-31503-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fehsenfeld, Sandra Quijada-Rodriguez, Alex R. Zhouyao, Haonan Durant, Andrea C. Donini, Andrew Sachs, Maria Eck, Peter Weihrauch, Dirk Hiat1 as a new transporter involved in ammonia regulation |
title | Hiat1 as a new transporter involved in ammonia regulation |
title_full | Hiat1 as a new transporter involved in ammonia regulation |
title_fullStr | Hiat1 as a new transporter involved in ammonia regulation |
title_full_unstemmed | Hiat1 as a new transporter involved in ammonia regulation |
title_short | Hiat1 as a new transporter involved in ammonia regulation |
title_sort | hiat1 as a new transporter involved in ammonia regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023664/ https://www.ncbi.nlm.nih.gov/pubmed/36932112 http://dx.doi.org/10.1038/s41598-023-31503-0 |
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