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From cyst to tubule: innovations in vertebrate spermatogenesis
Although vertebrates share many common traits, their germline development and function exhibit significant divergence. In particular, this article focuses on their spermatogenesis. The fundamental elements that constitute vertebrate spermatogenesis and the evolutionary changes that occurred upon tra...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley & Sons, Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049625/ https://www.ncbi.nlm.nih.gov/pubmed/26305780 http://dx.doi.org/10.1002/wdev.204 |
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author | Yoshida, Shosei |
author_facet | Yoshida, Shosei |
author_sort | Yoshida, Shosei |
collection | PubMed |
description | Although vertebrates share many common traits, their germline development and function exhibit significant divergence. In particular, this article focuses on their spermatogenesis. The fundamental elements that constitute vertebrate spermatogenesis and the evolutionary changes that occurred upon transition from water to land will be discussed. The life‐long continuity of spermatogenesis is supported by the function of stem cells. Series of mitotic and meiotic germ cell divisions are ‘incomplete’ due to incomplete cytokinesis, forming syncytia interconnected via intercellular bridges (ICBs). Throughout this process, germ cells are supported by appropriate microenvironments established primarily by somatic Sertoli cells. In anamniotes (fish and amphibians) spermatogenesis progresses in cysts, in which developing germ cell syncytia are individually encapsulated by Sertoli cells. Accordingly, Sertoli cells undergo turnover with germ cells that they nourish. This mode of cystic spermatogenesis is also observed in nonvertebrates as insects. In amniotes (reptiles, birds, and mammals), however, Sertoli cells do not turn over but comprise a persistent structure of seminiferous tubules. Sertoli cells nourish different stages of germ cells simultaneously in distinct regions of their surface. This function of Sertoli cells is spatiotemporally orchestrated, and the seminiferous epithelial cycle and spermatogenic wave make the seminiferous tubules a high‐throughput factory for sperm production. Furthermore, contrary to the organized differentiating cells, undifferentiated spermatogonia that comprise the stem cell compartment exhibit active motion over the basal layer of seminiferous tubules and the frequent breakdown of ICBs. Thus, amniote seminiferous tubules represent a typical facultative (or open) niche environment without a stem cell tethering anatomically defined niche. WIREs Dev Biol 2016, 5:119–131. doi: 10.1002/wdev.204 For further resources related to this article, please visit the WIREs website. |
format | Online Article Text |
id | pubmed-5049625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50496252016-10-06 From cyst to tubule: innovations in vertebrate spermatogenesis Yoshida, Shosei Wiley Interdiscip Rev Dev Biol Focus Article Although vertebrates share many common traits, their germline development and function exhibit significant divergence. In particular, this article focuses on their spermatogenesis. The fundamental elements that constitute vertebrate spermatogenesis and the evolutionary changes that occurred upon transition from water to land will be discussed. The life‐long continuity of spermatogenesis is supported by the function of stem cells. Series of mitotic and meiotic germ cell divisions are ‘incomplete’ due to incomplete cytokinesis, forming syncytia interconnected via intercellular bridges (ICBs). Throughout this process, germ cells are supported by appropriate microenvironments established primarily by somatic Sertoli cells. In anamniotes (fish and amphibians) spermatogenesis progresses in cysts, in which developing germ cell syncytia are individually encapsulated by Sertoli cells. Accordingly, Sertoli cells undergo turnover with germ cells that they nourish. This mode of cystic spermatogenesis is also observed in nonvertebrates as insects. In amniotes (reptiles, birds, and mammals), however, Sertoli cells do not turn over but comprise a persistent structure of seminiferous tubules. Sertoli cells nourish different stages of germ cells simultaneously in distinct regions of their surface. This function of Sertoli cells is spatiotemporally orchestrated, and the seminiferous epithelial cycle and spermatogenic wave make the seminiferous tubules a high‐throughput factory for sperm production. Furthermore, contrary to the organized differentiating cells, undifferentiated spermatogonia that comprise the stem cell compartment exhibit active motion over the basal layer of seminiferous tubules and the frequent breakdown of ICBs. Thus, amniote seminiferous tubules represent a typical facultative (or open) niche environment without a stem cell tethering anatomically defined niche. WIREs Dev Biol 2016, 5:119–131. doi: 10.1002/wdev.204 For further resources related to this article, please visit the WIREs website. John Wiley & Sons, Inc. 2016 2015-08-25 /pmc/articles/PMC5049625/ /pubmed/26305780 http://dx.doi.org/10.1002/wdev.204 Text en © 2015 The Authors. WIREs Developmental Biology published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Focus Article Yoshida, Shosei From cyst to tubule: innovations in vertebrate spermatogenesis |
title | From cyst to tubule: innovations in vertebrate spermatogenesis |
title_full | From cyst to tubule: innovations in vertebrate spermatogenesis |
title_fullStr | From cyst to tubule: innovations in vertebrate spermatogenesis |
title_full_unstemmed | From cyst to tubule: innovations in vertebrate spermatogenesis |
title_short | From cyst to tubule: innovations in vertebrate spermatogenesis |
title_sort | from cyst to tubule: innovations in vertebrate spermatogenesis |
topic | Focus Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049625/ https://www.ncbi.nlm.nih.gov/pubmed/26305780 http://dx.doi.org/10.1002/wdev.204 |
work_keys_str_mv | AT yoshidashosei fromcysttotubuleinnovationsinvertebratespermatogenesis |