Literature DB >> 8225836

The Sertoli-germ cell communication network in mammals.

B Jégou1.   

Abstract

As soon as scientists began to study testicular structure and function, the concept emerged that SCs and GCs communicate. We now know that the seminiferous epithelium is certainly one of the most complex tissues and that the structural and functional supports of SC-GC communication are extremely elaborate. At all stages of sexual maturation, somatic cells and GCs have developed a formidable set of communication devices that are involved in attachment, displacement, cell shaping, and cell-cell transfer of molecules and cellular materials. Some of the best morphologists since the nineteenth century have studied the anatomical basis of the SC-GC dialogue and have laid the foundations to the understanding of the spermatogenic process. Further experimental efforts are still being made. In particular, new data are emerging that have enabled scientists to go beyond the descriptional or deductive aspects and to tackle the mechanical aspects. From the functional point of view, significant progress has been made in deciphering SC-GC cell language. The unique strategic position of the SC allows this cell type to receive, integrate, and emit all the signals required for the spermatogenic process to or from the extratubular compartment (e.g., FSH, testosterone), the peritubular cells (e.g., P-Mod-S), and GCs themselves. Its location also allows it to coordinate GC activity in both the transversal and the longitudinal axes of the seminiferous tubule. The SC barrier and SC products create the physical and chemical microenvironments required for the completion of each of the different steps of spermatogenesis. In addition to the tubule fluid, the SC products directly or indirectly implicated in GC control are proteins, peptides, and steroid(s) involved in germ cell proliferation, differentiation, and metabolism; transport/binding proteins; proteases; extracellular matrix components; energy metabolites; antiproteases; and various membrane components. Sertoli cell polarization results from the existence of SC-SC occluding junctions. The products required for the mitotic phase of spermatogenesis may principally be secreted basally, whereas those required for meiotic division, spermiogenesis, and sperm cells may preferentially be secreted apically. The interaction between SC factors and GCs is mediated by GC membrane receptors and different endocytic processes. The GC secondary pathway(s) involved in SC action remains a mystery. Germ cell markers that would enable a precise assessment of SC influence are lacking. Changes in the composition of the GC complement and in GC size and shape, as well as GC divisions and migration, profoundly affect SC morphology and function.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8225836

Source DB:  PubMed          Journal:  Int Rev Cytol        ISSN: 0074-7696


  58 in total

1.  Excess type I interferon signaling in the mouse seminiferous tubules leads to germ cell loss and sterility.

Authors:  Anne-Pascale Satie; Severine Mazaud-Guittot; Isabelle Seif; Dominique Mahé; Zhiguo He; Guilhem Jouve; Bernard Jégou; Nathalie Dejucq-Rainsford
Journal:  J Biol Chem       Date:  2011-04-22       Impact factor: 5.157

Review 2.  Tubular fluid secretion in the seminiferous epithelium: ion transporters and aquaporins in Sertoli cells.

Authors:  Luís Rato; Sílvia Socorro; José E B Cavaco; Pedro F Oliveira
Journal:  J Membr Biol       Date:  2010-08-10       Impact factor: 1.843

3.  Loss of Dicer in Sertoli cells has a major impact on the testicular proteome of mice.

Authors:  Marilena D Papaioannou; Mélanie Lagarrigue; Charles E Vejnar; Antoine D Rolland; Françoise Kühne; Florence Aubry; Olivier Schaad; Alexandre Fort; Patrick Descombes; Marguerite Neerman-Arbez; Florian Guillou; Evgeny M Zdobnov; Charles Pineau; Serge Nef
Journal:  Mol Cell Proteomics       Date:  2010-05-13       Impact factor: 5.911

4.  Revisiting rat spermatogenesis with MALDI imaging at 20-microm resolution.

Authors:  Mélanie Lagarrigue; Michael Becker; Régis Lavigne; Sören-Oliver Deininger; Axel Walch; Florence Aubry; Detlev Suckau; Charles Pineau
Journal:  Mol Cell Proteomics       Date:  2010-12-12       Impact factor: 5.911

Review 5.  The Sertoli cell: one hundred fifty years of beauty and plasticity.

Authors:  L R França; R A Hess; J M Dufour; M C Hofmann; M D Griswold
Journal:  Andrology       Date:  2016-02-04       Impact factor: 3.842

Review 6.  Biology and regulation of ectoplasmic specialization, an atypical adherens junction type, in the testis.

Authors:  Elissa W P Wong; Dolores D Mruk; C Yan Cheng
Journal:  Biochim Biophys Acta       Date:  2007-11-19

Review 7.  Delivering non-hormonal contraceptives to men: advances and obstacles.

Authors:  Dolores D Mruk; C Yan Cheng
Journal:  Trends Biotechnol       Date:  2008-01-11       Impact factor: 19.536

8.  Sertoli cell Dicer is essential for spermatogenesis in mice.

Authors:  Marilena D Papaioannou; Jean-Luc Pitetti; Seungil Ro; Chanjae Park; Florence Aubry; Olivier Schaad; Charles E Vejnar; Francoise Kühne; Patrick Descombes; Evgeny M Zdobnov; Michael T McManus; Florian Guillou; Brian D Harfe; Wei Yan; Bernard Jégou; Serge Nef
Journal:  Dev Biol       Date:  2008-11-28       Impact factor: 3.582

Review 9.  Sterols in spermatogenesis and sperm maturation.

Authors:  Rok Keber; Damjana Rozman; Simon Horvat
Journal:  J Lipid Res       Date:  2012-10-23       Impact factor: 5.922

Review 10.  Properties, metabolism and roles of sulfogalactosylglycerolipid in male reproduction.

Authors:  Nongnuj Tanphaichitr; Kessiri Kongmanas; Kym F Faull; Julian Whitelegge; Federica Compostella; Naoko Goto-Inoue; James-Jules Linton; Brendon Doyle; Richard Oko; Hongbin Xu; Luigi Panza; Arpornrad Saewu
Journal:  Prog Lipid Res       Date:  2018-08-25       Impact factor: 16.195

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