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Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane
The mechano-electrical transduction (MET) channel of the inner ear receptor cells, termed hair cells, is a protein complex that enables our senses of hearing and balance. Hair cell MET requires an elaborate interplay of multiple proteins that form the MET channel. One of the MET complex components i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9925724/ https://www.ncbi.nlm.nih.gov/pubmed/36781873 http://dx.doi.org/10.1038/s41598-023-28045-w |
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author | Soler, David C. Ballesteros, Angela Sloan, Andrew E. McCormick, Thomas S. Stepanyan, Ruben |
author_facet | Soler, David C. Ballesteros, Angela Sloan, Andrew E. McCormick, Thomas S. Stepanyan, Ruben |
author_sort | Soler, David C. |
collection | PubMed |
description | The mechano-electrical transduction (MET) channel of the inner ear receptor cells, termed hair cells, is a protein complex that enables our senses of hearing and balance. Hair cell MET requires an elaborate interplay of multiple proteins that form the MET channel. One of the MET complex components is the transmembrane protein LHFPL5, which is required for hair cell MET and hearing. LHFPL5 is thought to form a multi-protein complex with other MET channel proteins, such as PCDH15, TMIE, and TMC1. Despite localizing to the plasma membrane of stereocilia, the mechanosensing organelles of hair cells, LHFPL5 requires its binding partner within the MET complex, PCDH15, to localize to the stereocilia tips in hair cells and to the plasma membrane in heterologous cells. Using the Aquaporin 3-tGFP reporter (AGR) for plasma membrane localization, we found that a region within extracellular loop 1, which interacts with PCDH15, precludes the trafficking of AGR reporter to the plasma membrane in heterologous cell lines. Our results suggest that the presence of protein partners may mask endoplasmic reticulum retention regions or enable the proper folding and trafficking of the MET complex components, to facilitate expression of the MET complex at the stereocilia membrane. |
format | Online Article Text |
id | pubmed-9925724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99257242023-02-15 Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane Soler, David C. Ballesteros, Angela Sloan, Andrew E. McCormick, Thomas S. Stepanyan, Ruben Sci Rep Article The mechano-electrical transduction (MET) channel of the inner ear receptor cells, termed hair cells, is a protein complex that enables our senses of hearing and balance. Hair cell MET requires an elaborate interplay of multiple proteins that form the MET channel. One of the MET complex components is the transmembrane protein LHFPL5, which is required for hair cell MET and hearing. LHFPL5 is thought to form a multi-protein complex with other MET channel proteins, such as PCDH15, TMIE, and TMC1. Despite localizing to the plasma membrane of stereocilia, the mechanosensing organelles of hair cells, LHFPL5 requires its binding partner within the MET complex, PCDH15, to localize to the stereocilia tips in hair cells and to the plasma membrane in heterologous cells. Using the Aquaporin 3-tGFP reporter (AGR) for plasma membrane localization, we found that a region within extracellular loop 1, which interacts with PCDH15, precludes the trafficking of AGR reporter to the plasma membrane in heterologous cell lines. Our results suggest that the presence of protein partners may mask endoplasmic reticulum retention regions or enable the proper folding and trafficking of the MET complex components, to facilitate expression of the MET complex at the stereocilia membrane. Nature Publishing Group UK 2023-02-13 /pmc/articles/PMC9925724/ /pubmed/36781873 http://dx.doi.org/10.1038/s41598-023-28045-w 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 Soler, David C. Ballesteros, Angela Sloan, Andrew E. McCormick, Thomas S. Stepanyan, Ruben Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane |
title | Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane |
title_full | Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane |
title_fullStr | Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane |
title_full_unstemmed | Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane |
title_short | Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane |
title_sort | multiple plasma membrane reporters discern lhfpl5 region that blocks trafficking to the plasma membrane |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9925724/ https://www.ncbi.nlm.nih.gov/pubmed/36781873 http://dx.doi.org/10.1038/s41598-023-28045-w |
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