Cargando…

In vivo autophagy and biogenesis of autophagosomes within male haploid cells during spermiogenesis

Autophagy is a unique catabolic pathway that is linked to several physiological processes. However, its role in the process of spermiogenesis is largely unknown. The aim of the current study was to determine the in vivo role of autophagy and the origin of autophagosome membrane biogenesis within mal...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Ping, Ahmed, Nisar, Wang, Lingling, Chen, Hong, Waqas, Yasir, Liu, Tengfei, Haseeb, Abdul, Bangulzai, Nasrullah, Huang, Yufei, Chen, Qiusheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593602/
https://www.ncbi.nlm.nih.gov/pubmed/28915631
http://dx.doi.org/10.18632/oncotarget.18221
_version_ 1783263070984863744
author Yang, Ping
Ahmed, Nisar
Wang, Lingling
Chen, Hong
Waqas, Yasir
Liu, Tengfei
Haseeb, Abdul
Bangulzai, Nasrullah
Huang, Yufei
Chen, Qiusheng
author_facet Yang, Ping
Ahmed, Nisar
Wang, Lingling
Chen, Hong
Waqas, Yasir
Liu, Tengfei
Haseeb, Abdul
Bangulzai, Nasrullah
Huang, Yufei
Chen, Qiusheng
author_sort Yang, Ping
collection PubMed
description Autophagy is a unique catabolic pathway that is linked to several physiological processes. However, its role in the process of spermiogenesis is largely unknown. The aim of the current study was to determine the in vivo role of autophagy and the origin of autophagosome membrane biogenesis within male haploid cells. Our immunohistochemistry results demonstrated that LC3 and ATG7 localization were increased dramatically in round to elongated spermatids (haploid cells) towards the lumen of seminiferous tubules, however, poorly expressed in the early stages of germ cells near the basal membrane. Moreover, transmission electron microscopy revealed that the numbers of lysosomes and autophagosomes increased in the elongated spermatids as spermiogenesis progressed. However, no evidence was found for the presence of autophagosomes in the Sertoli cells, spermatogonia or early primary spermatocytes (diploid cells). Furthermore, TEM showed that many endoplasmic reticula were transformed into a “chrysanthemum flower center,” from which a double-layered isolation membrane appeared to develop into an autophagosome. This study provides novel evidence about the formation of autophagosomes through the chrysanthemum flower center from the endoplasmic reticulum, and suggests that autophagy may have an important role in the removal of extra cytoplasm within male haploid cells during spermiogenesis.
format Online
Article
Text
id pubmed-5593602
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-55936022017-09-14 In vivo autophagy and biogenesis of autophagosomes within male haploid cells during spermiogenesis Yang, Ping Ahmed, Nisar Wang, Lingling Chen, Hong Waqas, Yasir Liu, Tengfei Haseeb, Abdul Bangulzai, Nasrullah Huang, Yufei Chen, Qiusheng Oncotarget Research Paper Autophagy is a unique catabolic pathway that is linked to several physiological processes. However, its role in the process of spermiogenesis is largely unknown. The aim of the current study was to determine the in vivo role of autophagy and the origin of autophagosome membrane biogenesis within male haploid cells. Our immunohistochemistry results demonstrated that LC3 and ATG7 localization were increased dramatically in round to elongated spermatids (haploid cells) towards the lumen of seminiferous tubules, however, poorly expressed in the early stages of germ cells near the basal membrane. Moreover, transmission electron microscopy revealed that the numbers of lysosomes and autophagosomes increased in the elongated spermatids as spermiogenesis progressed. However, no evidence was found for the presence of autophagosomes in the Sertoli cells, spermatogonia or early primary spermatocytes (diploid cells). Furthermore, TEM showed that many endoplasmic reticula were transformed into a “chrysanthemum flower center,” from which a double-layered isolation membrane appeared to develop into an autophagosome. This study provides novel evidence about the formation of autophagosomes through the chrysanthemum flower center from the endoplasmic reticulum, and suggests that autophagy may have an important role in the removal of extra cytoplasm within male haploid cells during spermiogenesis. Impact Journals LLC 2017-05-26 /pmc/articles/PMC5593602/ /pubmed/28915631 http://dx.doi.org/10.18632/oncotarget.18221 Text en Copyright: © 2017 Yang et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Yang, Ping
Ahmed, Nisar
Wang, Lingling
Chen, Hong
Waqas, Yasir
Liu, Tengfei
Haseeb, Abdul
Bangulzai, Nasrullah
Huang, Yufei
Chen, Qiusheng
In vivo autophagy and biogenesis of autophagosomes within male haploid cells during spermiogenesis
title In vivo autophagy and biogenesis of autophagosomes within male haploid cells during spermiogenesis
title_full In vivo autophagy and biogenesis of autophagosomes within male haploid cells during spermiogenesis
title_fullStr In vivo autophagy and biogenesis of autophagosomes within male haploid cells during spermiogenesis
title_full_unstemmed In vivo autophagy and biogenesis of autophagosomes within male haploid cells during spermiogenesis
title_short In vivo autophagy and biogenesis of autophagosomes within male haploid cells during spermiogenesis
title_sort in vivo autophagy and biogenesis of autophagosomes within male haploid cells during spermiogenesis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593602/
https://www.ncbi.nlm.nih.gov/pubmed/28915631
http://dx.doi.org/10.18632/oncotarget.18221
work_keys_str_mv AT yangping invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis
AT ahmednisar invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis
AT wanglingling invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis
AT chenhong invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis
AT waqasyasir invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis
AT liutengfei invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis
AT haseebabdul invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis
AT bangulzainasrullah invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis
AT huangyufei invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis
AT chenqiusheng invivoautophagyandbiogenesisofautophagosomeswithinmalehaploidcellsduringspermiogenesis