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The TRPV3 channel of the bovine rumen: localization and functional characterization of a protein relevant for ruminal ammonia transport

Large quantities of ammonia (NH(3) or NH(4)(+)) are absorbed from the gut, associated with encephalitis in hepatic disease, poor protein efficiency in livestock, and emissions of nitrogenous climate gasses. Identifying the transport mechanisms appears urgent. Recent functional and mRNA data suggest...

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Autores principales: Liebe, Franziska, Liebe, Hendrik, Kaessmeyer, Sabine, Sponder, Gerhard, Stumpff, Friederike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293678/
https://www.ncbi.nlm.nih.gov/pubmed/32458085
http://dx.doi.org/10.1007/s00424-020-02393-2
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author Liebe, Franziska
Liebe, Hendrik
Kaessmeyer, Sabine
Sponder, Gerhard
Stumpff, Friederike
author_facet Liebe, Franziska
Liebe, Hendrik
Kaessmeyer, Sabine
Sponder, Gerhard
Stumpff, Friederike
author_sort Liebe, Franziska
collection PubMed
description Large quantities of ammonia (NH(3) or NH(4)(+)) are absorbed from the gut, associated with encephalitis in hepatic disease, poor protein efficiency in livestock, and emissions of nitrogenous climate gasses. Identifying the transport mechanisms appears urgent. Recent functional and mRNA data suggest that absorption of ammonia from the forestomach of cattle may involve TRPV3 channels. The purpose of the present study was to sequence the bovine homologue of TRPV3 (bTRPV3), localize the protein in ruminal tissue, and confirm transport of NH(4)(+). After sequencing, bTRPV3 was overexpressed in HEK-293 cells and Xenopus oocytes. An antibody was selected via epitope screening and used to detect the protein in immunoblots of overexpressing cells and bovine rumen, revealing a signal of the predicted ~ 90 kDa. In rumen only, an additional ~ 60 kDa band appeared, which may represent a previously described bTRPV3 splice variant of equal length. Immunohistochemistry revealed staining from the ruminal stratum basale to stratum granulosum. Measurements with pH-sensitive microelectrodes showed that NH(4)(+) acidifies Xenopus oocytes, with overexpression of bTRPV3 enhancing permeability to NH(4)(+). Single-channel measurements revealed that Xenopus oocytes endogenously expressed small cation channels in addition to fourfold-larger channels only observed after expression of bTRPV3. Both endogenous and bTRPV3 channels conducted NH(4)(+), Na(+), and K(+). We conclude that bTRPV3 is expressed by the ruminal epithelium on the protein level. In conjunction with data from previous studies, a role in the transport of Na(+), Ca(2+), and NH(4)(+) emerges. Consequences for calcium homeostasis, ruminal pH, and nitrogen efficiency in cattle are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00424-020-02393-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-72936782020-06-16 The TRPV3 channel of the bovine rumen: localization and functional characterization of a protein relevant for ruminal ammonia transport Liebe, Franziska Liebe, Hendrik Kaessmeyer, Sabine Sponder, Gerhard Stumpff, Friederike Pflugers Arch Ion Channels, Receptors and Transporters Large quantities of ammonia (NH(3) or NH(4)(+)) are absorbed from the gut, associated with encephalitis in hepatic disease, poor protein efficiency in livestock, and emissions of nitrogenous climate gasses. Identifying the transport mechanisms appears urgent. Recent functional and mRNA data suggest that absorption of ammonia from the forestomach of cattle may involve TRPV3 channels. The purpose of the present study was to sequence the bovine homologue of TRPV3 (bTRPV3), localize the protein in ruminal tissue, and confirm transport of NH(4)(+). After sequencing, bTRPV3 was overexpressed in HEK-293 cells and Xenopus oocytes. An antibody was selected via epitope screening and used to detect the protein in immunoblots of overexpressing cells and bovine rumen, revealing a signal of the predicted ~ 90 kDa. In rumen only, an additional ~ 60 kDa band appeared, which may represent a previously described bTRPV3 splice variant of equal length. Immunohistochemistry revealed staining from the ruminal stratum basale to stratum granulosum. Measurements with pH-sensitive microelectrodes showed that NH(4)(+) acidifies Xenopus oocytes, with overexpression of bTRPV3 enhancing permeability to NH(4)(+). Single-channel measurements revealed that Xenopus oocytes endogenously expressed small cation channels in addition to fourfold-larger channels only observed after expression of bTRPV3. Both endogenous and bTRPV3 channels conducted NH(4)(+), Na(+), and K(+). We conclude that bTRPV3 is expressed by the ruminal epithelium on the protein level. In conjunction with data from previous studies, a role in the transport of Na(+), Ca(2+), and NH(4)(+) emerges. Consequences for calcium homeostasis, ruminal pH, and nitrogen efficiency in cattle are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00424-020-02393-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-05-26 2020 /pmc/articles/PMC7293678/ /pubmed/32458085 http://dx.doi.org/10.1007/s00424-020-02393-2 Text en © The Author(s) 2020 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/.
spellingShingle Ion Channels, Receptors and Transporters
Liebe, Franziska
Liebe, Hendrik
Kaessmeyer, Sabine
Sponder, Gerhard
Stumpff, Friederike
The TRPV3 channel of the bovine rumen: localization and functional characterization of a protein relevant for ruminal ammonia transport
title The TRPV3 channel of the bovine rumen: localization and functional characterization of a protein relevant for ruminal ammonia transport
title_full The TRPV3 channel of the bovine rumen: localization and functional characterization of a protein relevant for ruminal ammonia transport
title_fullStr The TRPV3 channel of the bovine rumen: localization and functional characterization of a protein relevant for ruminal ammonia transport
title_full_unstemmed The TRPV3 channel of the bovine rumen: localization and functional characterization of a protein relevant for ruminal ammonia transport
title_short The TRPV3 channel of the bovine rumen: localization and functional characterization of a protein relevant for ruminal ammonia transport
title_sort trpv3 channel of the bovine rumen: localization and functional characterization of a protein relevant for ruminal ammonia transport
topic Ion Channels, Receptors and Transporters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293678/
https://www.ncbi.nlm.nih.gov/pubmed/32458085
http://dx.doi.org/10.1007/s00424-020-02393-2
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