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N-WASP Is Required for Structural Integrity of the Blood-Testis Barrier

During spermatogenesis, the blood-testis barrier (BTB) segregates the adluminal (apical) and basal compartments in the seminiferous epithelium, thereby creating a privileged adluminal environment that allows post-meiotic spermatid development to proceed without interference of the host immune system...

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Autores principales: Xiao, Xiang, Mruk, Dolores D., Tang, Elizabeth I., Massarwa, R'ada, Mok, Ka Wai, Li, Nan, Wong, Chris K. C., Lee, Will M., Snapper, Scott B., Shilo, Ben-Zion, Schejter, Eyal D., Cheng, C. Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072540/
https://www.ncbi.nlm.nih.gov/pubmed/24967734
http://dx.doi.org/10.1371/journal.pgen.1004447
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author Xiao, Xiang
Mruk, Dolores D.
Tang, Elizabeth I.
Massarwa, R'ada
Mok, Ka Wai
Li, Nan
Wong, Chris K. C.
Lee, Will M.
Snapper, Scott B.
Shilo, Ben-Zion
Schejter, Eyal D.
Cheng, C. Yan
author_facet Xiao, Xiang
Mruk, Dolores D.
Tang, Elizabeth I.
Massarwa, R'ada
Mok, Ka Wai
Li, Nan
Wong, Chris K. C.
Lee, Will M.
Snapper, Scott B.
Shilo, Ben-Zion
Schejter, Eyal D.
Cheng, C. Yan
author_sort Xiao, Xiang
collection PubMed
description During spermatogenesis, the blood-testis barrier (BTB) segregates the adluminal (apical) and basal compartments in the seminiferous epithelium, thereby creating a privileged adluminal environment that allows post-meiotic spermatid development to proceed without interference of the host immune system. A key feature of the BTB is its continuous remodeling within the Sertoli cells, the major somatic component of the seminiferous epithelium. This remodeling is necessary to allow the transport of germ cells towards the seminiferous tubule interior, while maintaining intact barrier properties. Here we demonstrate that the actin nucleation promoting factor Neuronal Wiskott-Aldrich Syndrome Protein (N-WASP) provides an essential function necessary for BTB restructuring, and for maintaining spermatogenesis. Our data suggests that the N-WASP-Arp2/3 actin polymerization machinery generates branched-actin arrays at an advanced stage of BTB remodeling. These arrays are proposed to mediate the restructuring process through endocytic recycling of BTB components. Disruption of N-WASP in Sertoli cells results in major structural abnormalities to the BTB, including mis-localization of critical junctional and cytoskeletal elements, and leads to disruption of barrier function. These impairments result in a complete arrest of spermatogenesis, underscoring the critical involvement of the somatic compartment of the seminiferous tubules in germ cell maturation.
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spelling pubmed-40725402014-07-02 N-WASP Is Required for Structural Integrity of the Blood-Testis Barrier Xiao, Xiang Mruk, Dolores D. Tang, Elizabeth I. Massarwa, R'ada Mok, Ka Wai Li, Nan Wong, Chris K. C. Lee, Will M. Snapper, Scott B. Shilo, Ben-Zion Schejter, Eyal D. Cheng, C. Yan PLoS Genet Research Article During spermatogenesis, the blood-testis barrier (BTB) segregates the adluminal (apical) and basal compartments in the seminiferous epithelium, thereby creating a privileged adluminal environment that allows post-meiotic spermatid development to proceed without interference of the host immune system. A key feature of the BTB is its continuous remodeling within the Sertoli cells, the major somatic component of the seminiferous epithelium. This remodeling is necessary to allow the transport of germ cells towards the seminiferous tubule interior, while maintaining intact barrier properties. Here we demonstrate that the actin nucleation promoting factor Neuronal Wiskott-Aldrich Syndrome Protein (N-WASP) provides an essential function necessary for BTB restructuring, and for maintaining spermatogenesis. Our data suggests that the N-WASP-Arp2/3 actin polymerization machinery generates branched-actin arrays at an advanced stage of BTB remodeling. These arrays are proposed to mediate the restructuring process through endocytic recycling of BTB components. Disruption of N-WASP in Sertoli cells results in major structural abnormalities to the BTB, including mis-localization of critical junctional and cytoskeletal elements, and leads to disruption of barrier function. These impairments result in a complete arrest of spermatogenesis, underscoring the critical involvement of the somatic compartment of the seminiferous tubules in germ cell maturation. Public Library of Science 2014-06-26 /pmc/articles/PMC4072540/ /pubmed/24967734 http://dx.doi.org/10.1371/journal.pgen.1004447 Text en © 2014 Xiao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Xiao, Xiang
Mruk, Dolores D.
Tang, Elizabeth I.
Massarwa, R'ada
Mok, Ka Wai
Li, Nan
Wong, Chris K. C.
Lee, Will M.
Snapper, Scott B.
Shilo, Ben-Zion
Schejter, Eyal D.
Cheng, C. Yan
N-WASP Is Required for Structural Integrity of the Blood-Testis Barrier
title N-WASP Is Required for Structural Integrity of the Blood-Testis Barrier
title_full N-WASP Is Required for Structural Integrity of the Blood-Testis Barrier
title_fullStr N-WASP Is Required for Structural Integrity of the Blood-Testis Barrier
title_full_unstemmed N-WASP Is Required for Structural Integrity of the Blood-Testis Barrier
title_short N-WASP Is Required for Structural Integrity of the Blood-Testis Barrier
title_sort n-wasp is required for structural integrity of the blood-testis barrier
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072540/
https://www.ncbi.nlm.nih.gov/pubmed/24967734
http://dx.doi.org/10.1371/journal.pgen.1004447
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