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LCRMP-1 is required for spermatogenesis and stabilises spermatid F-actin organization via the PI3K-Akt pathway
Long-form collapsin response mediator protein-1 (LCRMP-1) belongs to the CRMP family which comprises brain-enriched proteins responsible for axon guidance. However, its role in spermatogenesis remains unclear. Here we find that LCRMP-1 is abundantly expressed in the testis. To characterize its physi...
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/PMC10086033/ https://www.ncbi.nlm.nih.gov/pubmed/37037996 http://dx.doi.org/10.1038/s42003-023-04778-2 |
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author | Chang, Jung-Hsuan Chou, Chia-Hua Wu, Jui-Ching Liao, Keng-Mao Luo, Wei-Jia Hsu, Wei-Lun Chen, Xuan-Ren Yu, Sung-Liang Pan, Szu-Hua Yang, Pan-Chyr Su, Kang-Yi |
author_facet | Chang, Jung-Hsuan Chou, Chia-Hua Wu, Jui-Ching Liao, Keng-Mao Luo, Wei-Jia Hsu, Wei-Lun Chen, Xuan-Ren Yu, Sung-Liang Pan, Szu-Hua Yang, Pan-Chyr Su, Kang-Yi |
author_sort | Chang, Jung-Hsuan |
collection | PubMed |
description | Long-form collapsin response mediator protein-1 (LCRMP-1) belongs to the CRMP family which comprises brain-enriched proteins responsible for axon guidance. However, its role in spermatogenesis remains unclear. Here we find that LCRMP-1 is abundantly expressed in the testis. To characterize its physiological function, we generate LCRMP-1-deficient mice (Lcrmp-1(−/−)). These mice exhibit aberrant spermiation with apoptotic spermatids, oligospermia, and accumulation of immature testicular cells, contributing to reduced fertility. In the seminiferous epithelial cycle, LCRMP-1 expression pattern varies in a stage-dependent manner. LCRMP-1 is highly expressed in spermatids during spermatogenesis and especially localized to the spermiation machinery during spermiation. Mechanistically, LCRMP-1 deficiency causes disorganized F-actin due to unbalanced signaling of F-actin dynamics through upregulated PI3K-Akt-mTOR signaling. In conclusion, LCRMP-1 maintains spermatogenesis homeostasis by modulating cytoskeleton remodeling for spermatozoa release. |
format | Online Article Text |
id | pubmed-10086033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100860332023-04-12 LCRMP-1 is required for spermatogenesis and stabilises spermatid F-actin organization via the PI3K-Akt pathway Chang, Jung-Hsuan Chou, Chia-Hua Wu, Jui-Ching Liao, Keng-Mao Luo, Wei-Jia Hsu, Wei-Lun Chen, Xuan-Ren Yu, Sung-Liang Pan, Szu-Hua Yang, Pan-Chyr Su, Kang-Yi Commun Biol Article Long-form collapsin response mediator protein-1 (LCRMP-1) belongs to the CRMP family which comprises brain-enriched proteins responsible for axon guidance. However, its role in spermatogenesis remains unclear. Here we find that LCRMP-1 is abundantly expressed in the testis. To characterize its physiological function, we generate LCRMP-1-deficient mice (Lcrmp-1(−/−)). These mice exhibit aberrant spermiation with apoptotic spermatids, oligospermia, and accumulation of immature testicular cells, contributing to reduced fertility. In the seminiferous epithelial cycle, LCRMP-1 expression pattern varies in a stage-dependent manner. LCRMP-1 is highly expressed in spermatids during spermatogenesis and especially localized to the spermiation machinery during spermiation. Mechanistically, LCRMP-1 deficiency causes disorganized F-actin due to unbalanced signaling of F-actin dynamics through upregulated PI3K-Akt-mTOR signaling. In conclusion, LCRMP-1 maintains spermatogenesis homeostasis by modulating cytoskeleton remodeling for spermatozoa release. Nature Publishing Group UK 2023-04-10 /pmc/articles/PMC10086033/ /pubmed/37037996 http://dx.doi.org/10.1038/s42003-023-04778-2 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chang, Jung-Hsuan Chou, Chia-Hua Wu, Jui-Ching Liao, Keng-Mao Luo, Wei-Jia Hsu, Wei-Lun Chen, Xuan-Ren Yu, Sung-Liang Pan, Szu-Hua Yang, Pan-Chyr Su, Kang-Yi LCRMP-1 is required for spermatogenesis and stabilises spermatid F-actin organization via the PI3K-Akt pathway |
title | LCRMP-1 is required for spermatogenesis and stabilises spermatid F-actin organization via the PI3K-Akt pathway |
title_full | LCRMP-1 is required for spermatogenesis and stabilises spermatid F-actin organization via the PI3K-Akt pathway |
title_fullStr | LCRMP-1 is required for spermatogenesis and stabilises spermatid F-actin organization via the PI3K-Akt pathway |
title_full_unstemmed | LCRMP-1 is required for spermatogenesis and stabilises spermatid F-actin organization via the PI3K-Akt pathway |
title_short | LCRMP-1 is required for spermatogenesis and stabilises spermatid F-actin organization via the PI3K-Akt pathway |
title_sort | lcrmp-1 is required for spermatogenesis and stabilises spermatid f-actin organization via the pi3k-akt pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086033/ https://www.ncbi.nlm.nih.gov/pubmed/37037996 http://dx.doi.org/10.1038/s42003-023-04778-2 |
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