Literature DB >> 3526980

Distribution of actin in Sertoli cell ectoplasmic specializations and associated spermatids in the ground squirrel testis.

A W Vogl, B D Grove, G J Lew.   

Abstract

We have investigated the possibility that the complex patterns of fluorescence associated with spermatids of the ground squirrel labeled with 7-nitrobenz-2-oxa-1,3-diazole-phallacidin (NBD-phallacidin) are due to the presence of filamentous actin within the spermatids themselves rather than to actin in attached Sertoli cell ectoplasmic specializations, as previously reported (J. Cell Biol., 100:814-825). Enzymatic treatments (trypsin, DNAase 1) freed Sertoli cell ectoplasmic specializations from spermatids and resulted in a loss, from the spermatids, of the complex fluorescence patterns, suggesting that the latter were generated by labeled actin in ectoplasmic specializations. Moreover, ectoplasmic specializations that were detached enzymatically from spermatids demonstrated the same fluorescence patterns as those emitted from spermatids in the intact or mechanically fragmented seminiferous epithelium. Most spermatids, however, do display a weak and diffuse pattern of fluorescence that changes during spermatogenesis and that is localized between the acrosomal cap and nucleus. S-1 decoration confirmed this subacrosomal localization and further demonstrated that the actin in adjacent Sertoli cell ectoplasmic specializations is arranged in a unipolar fashion. We conclude that the complex patterns of actin fluorescence associated with mechanically isolated spermatids are a superimposition of both Sertoli cell and germ cell actin; however, the latter is either poorly detected or not detected at all when Sertoli cell ectoplasmic specializations overlie the germ cells.

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Year:  1986        PMID: 3526980     DOI: 10.1002/ar.1092150402

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


  6 in total

1.  A missense mutation in the Capza3 gene and disruption of F-actin organization in spermatids of repro32 infertile male mice.

Authors:  Christopher B Geyer; Amy L Inselman; Jeffrey A Sunman; Sheila Bornstein; Mary Ann Handel; Edward M Eddy
Journal:  Dev Biol       Date:  2009-03-31       Impact factor: 3.582

2.  Comparison of LR white resin, Lowicryl K4M and Epon postembedding procedures for immunogold staining of actin in the testis.

Authors:  M L Kann; J P Fouquet
Journal:  Histochemistry       Date:  1989

3.  Autophagy is required for ectoplasmic specialization assembly in sertoli cells.

Authors:  Chao Liu; Hongna Wang; Yongliang Shang; Weixiao Liu; Zhenhua Song; Haichao Zhao; Lina Wang; Pengfei Jia; Fengyi Gao; Zhiliang Xu; Lin Yang; Fei Gao; Wei Li
Journal:  Autophagy       Date:  2016-03-17       Impact factor: 16.016

4.  Stage-specific localization of cytoskeletal actin mRNA in murine seminiferous tubules and intestinal epithelia as demonstrated by in-situ hybridization.

Authors:  S Sakiyama; Y Nakamura; K Tokunaga; H Takazawa; Y Ohwaki; T Nagano
Journal:  Cell Tissue Res       Date:  1989-11       Impact factor: 5.249

5.  Distribution of actin-filament bundles in myoid cells, Sertoli cells, and tunica albuginea of rat and mouse testes.

Authors:  M Maekawa; T Nagano; K Kamimura; T Murakami; H Ishikawa; M Dezawa
Journal:  Cell Tissue Res       Date:  1991-11       Impact factor: 5.249

6.  Claudin 11 deficiency in mice results in loss of the Sertoli cell epithelial phenotype in the testis.

Authors:  S Mazaud-Guittot; E Meugnier; S Pesenti; X Wu; H Vidal; A Gow; B Le Magueresse-Battistoni
Journal:  Biol Reprod       Date:  2009-09-09       Impact factor: 4.285

  6 in total

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