Literature DB >> 7992888

Sertoli cells in testes containing or lacking germ cells: a comparative study of paracrine effects using the W (c-kit) gene mutant mouse model.

L R De Franca1, A Bartke, K E Borg, M Cecim, C T Fadden, A Yagi, L D Russell.   

Abstract

BACKGROUND: Paracrine effects of germ cells on Sertoli cell structure were examined in a mouse model with the W locus (dominant white spotting) mutation in which animals with the W/Wv genotype (referred to as mutants) lack virtually all germ cells.
RESULTS: Morphometric determination of Sertoli cell parameters in mutant and control (+/+) animals showed that although the testes of mutant animals were about eight times smaller than controls, the numbers of Sertoli cells in the two groups did not differ. Sertoli cell volume, Sertoli cell cytoplasmic and nuclear volumes, and Sertoli cell surface area in mutant animals were significantly smaller than in control animals. Organelle volumes and surface areas, expressed per cell, did not differ significantly in the two groups with one exception: the volume and surface area of smooth endoplasmic reticulum was significantly reduced in mutant animals. Plasma testosterone levels and tissue testosterone levels/testis were normal, indicating that the effects observed in the mutant animal were not a consequence of androgen insufficiency. Plasma FSH was elevated, probably as a consequence of germ cell depletion, and was thought not to affect Sertoli cell parameters observed.
CONCLUSIONS: The data suggest that paracrine interactions with germ cells do affect Sertoli cells by modifying the amount of smooth endoplasmic reticulum. These data focus attention on the function of this abundant Sertoli cell organelle in promoting spermatogenesis.

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Year:  1994        PMID: 7992888     DOI: 10.1002/ar.1092400209

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


  10 in total

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Authors:  Jose R Rodriguez-Sosa; Guilherme M J Costa; Rahul Rathi; Luiz R França; Ina Dobrinski
Journal:  Reproduction       Date:  2012-05-01       Impact factor: 3.906

2.  ERM is required for transcriptional control of the spermatogonial stem cell niche.

Authors:  Chen Chen; Wenjun Ouyang; Vadim Grigura; Qing Zhou; Kay Carnes; Hyunjung Lim; Guang-Quan Zhao; Silvia Arber; Natasza Kurpios; Theresa L Murphy; Alec M Cheng; John A Hassell; Varadaraj Chandrashekar; Marie-Claude Hofmann; Rex A Hess; Kenneth M Murphy
Journal:  Nature       Date:  2005-08-18       Impact factor: 49.962

3.  Selective ablation of the androgen receptor in mouse sertoli cells affects sertoli cell maturation, barrier formation and cytoskeletal development.

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Journal:  PLoS One       Date:  2010-11-30       Impact factor: 3.240

Review 4.  Androgen receptor (AR) physiological roles in male and female reproductive systems: lessons learned from AR-knockout mice lacking AR in selective cells.

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5.  Androgen action via testicular peritubular myoid cells is essential for male fertility.

Authors:  Michelle Welsh; Philippa T K Saunders; Nina Atanassova; Richard M Sharpe; Lee B Smith
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6.  Effect of germ cell depletion on levels of specific mRNA transcripts in mouse Sertoli cells and Leydig cells.

Authors:  P J O'Shaughnessy; L Hu; P J Baker
Journal:  Reproduction       Date:  2008-04-04       Impact factor: 3.906

7.  Comparison of Neonatal and Adult Mice-derived Sertoli Cells in Support of Expansion of Mouse Spermatogonial Stem Cells In vitro.

Authors:  Faranak Tavakolifar; Abdolhossein Shahverdi; Mehdi Pirouz; Malak Shakeri; Morteza Koruji; Hossein Baharvand
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Review 8.  Cell-specific ablation in the testis: what have we learned?

Authors:  L B Smith; P J O'Shaughnessy; D Rebourcet
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9.  Disruption of c-Kit Signaling in Kit(W-sh/W-sh) Growing Mice Increases Bone Turnover.

Authors:  Sutada Lotinun; Nateetip Krishnamra
Journal:  Sci Rep       Date:  2016-08-16       Impact factor: 4.379

10.  Changes in Expression of Specific mRNA Transcripts after Single- or Re-Irradiation in Mouse Testes.

Authors:  Kenta Nagahori; Ning Qu; Miyuki Kuramasu; Yuki Ogawa; Daisuke Kiyoshima; Kaori Suyama; Shogo Hayashi; Kou Sakabe; Takayuki Yoshimoto; Masahiro Itoh
Journal:  Genes (Basel)       Date:  2022-01-15       Impact factor: 4.096

  10 in total

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