Literature DB >> 10486516

Three-dimensional structure of the Golgi apparatus in mouse spermatids: a scanning electron microscopic study.

H C Ho1, C Y Tang, S S Suarez.   

Abstract

In this study, the three-dimensional organization of the Golgi apparatus in mouse spermatids was elucidated by preparing testicular tissue with the osmium-DMSO-osmium method and examining it by stereo-scanning electron microscopy. The cis-most saccule was found to be a regular network of anastomotic membranous tubules covered by a single cisterna of ER. The trans-Golgi network was seen to be composed of irregular saccules perforated by pores at the edge. It appears that the anastomosing trans-Golgi network breaks down into strings of connected vesicles which arise from the edge of the saccules during the cap phase of spermiogenesis. Many apparently individual vesicles seen in thin sections through the trans-Golgi network are actually joined in continuous strings. This was the first time that these structures could be visualized directly without three-dimensional image reconstruction. By correlating the morphology of the Golgi apparatus with the stage of acrosome formation, the Golgi cisternae were found to change dynamically in a cis-trans direction from fenestrated saccules to continuous strings of vesicles, which finally dissipated as transport vesicles at the trans aspect. This suggests that the hypothetical model of cisternal maturation, which dictates that cargo moves through the Golgi apparatus without leaving the cisternal lumen and the secretion occurs by progressive maturation of the Golgi cisternae as they move in the cis-trans direction, may be applicable to acrosome formation. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10486516     DOI: 10.1002/(SICI)1097-0185(19991001)256:2<189::AID-AR9>3.0.CO;2-I

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  5 in total

1.  Bicarbonate induces membrane reorganization and CBR1 and TRPV1 endocannabinoid receptor migration in lipid microdomains in capacitating boar spermatozoa.

Authors:  Laura Botto; Nicola Bernabò; Paola Palestini; Barbara Barboni
Journal:  J Membr Biol       Date:  2010-11-23       Impact factor: 1.843

2.  Biochemical characterization of membrane fractions in murine sperm: identification of three distinct sub-types of membrane rafts.

Authors:  Atsushi Asano; Vimal Selvaraj; Danielle E Buttke; Jacquelyn L Nelson; Karin M Green; James E Evans; Alexander J Travis
Journal:  J Cell Physiol       Date:  2009-03       Impact factor: 6.384

3.  Cellular and subcellular localization of endogenous phospholipase D6 in seminiferous tubules of mouse testes.

Authors:  Mun-Yong Lee; Do Sik Min; Tae-Ryong Riew; Soojin Kim; Xuyan Jin; Hong Lim Kim; Won Chan Hwang; Minju Kang; Eun Sun Yang
Journal:  Cell Tissue Res       Date:  2021-03-30       Impact factor: 5.249

4.  Analysis of Ser/Thr Kinase HASPIN-Interacting Proteins in the Spermatids.

Authors:  Naoko Maeda; Junji Tsuchida; Yoshitake Nishimune; Hiromitsu Tanaka
Journal:  Int J Mol Sci       Date:  2022-08-13       Impact factor: 6.208

5.  FAM209 associates with DPY19L2, and is required for sperm acrosome biogenesis and fertility in mice.

Authors:  Julio M Castaneda; Keisuke Shimada; Yuhkoh Satouh; Zhifeng Yu; Darius J Devlin; Masahito Ikawa; Martin M Matzuk
Journal:  J Cell Sci       Date:  2021-11-01       Impact factor: 5.285

  5 in total

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