Literature DB >> 18544902

Continual maintenance of the blood-testis barrier during spermatogenesis: the intermediate compartment theory revisited.

Futoshi Yazama1.   

Abstract

Tight junctions occur between the lateral processes of neighboring Sertoli cells that divide the seminiferous epithelium into two compartments: basal and adluminal compartments. These tight junctions constitute the blood-testis barrier (BTB). The established theory that the BTB must open when spermatocytes translocate from the basal compartment to the adluminal compartment is marked by one contradiction, that is, normal spermatogenesis occurs in the testis because the BTB is expected to constantly seclude the adluminal compartment from the basal compartment in order to protect haploid germ cells from the autoimmune system. Subsequently, another concept was proposed in which two BTBs divide the seminiferous epithelium into three compartments: basal, intermediate and adluminal compartments. It has been suggested that the transition from the basal region to the adluminal region without the BTB open occurs through the agency of a short-lived intermediate compartment embodying some primary spermatocytes. In contrast, the results of recent findings in the molecular architecture of the BTB suggest that the BTB in the seminiferous epithelium must "open". In this paper, I re-examine the BTBs of boar and experimental cryptorchid mouse testes by transmission electron microscope (TEM). TEM analysis showed that an atypical basal compartment existed in the thin seminiferous epithelium of 14-day post-cryptorchid mice testes. In developmental boar testes, ectoplasmic specialization (ES) of the seminiferous epithelium showed dynamic behavior. The intermediate compartment was clearly observed between the basal and adluminal compartments of the mature boar seminiferous epithelium. ESs were observed between Sertoli cells and spermatids at all developmental stages, including early, late and mature. Furthermore, ESs were situated on the apical surface of the seminiferous epithelium. From these results, I propose that the BTB is continually maintained during spermatogenesis and suggest a model of ES circulation in the seminiferous epithelium.

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Year:  2008        PMID: 18544902     DOI: 10.1262/jrd.19169

Source DB:  PubMed          Journal:  J Reprod Dev        ISSN: 0916-8818            Impact factor:   2.214


  7 in total

Review 1.  Intercellular adhesion molecules (ICAMs) and spermatogenesis.

Authors:  Xiang Xiao; Dolores D Mruk; C Yan Cheng
Journal:  Hum Reprod Update       Date:  2013-01-03       Impact factor: 15.610

2.  Characterization and functionality of proliferative human Sertoli cells.

Authors:  Kitty Chui; Alpa Trivedi; C Yan Cheng; Diana B Cherbavaz; Paul F Dazin; Ai Lam Thu Huynh; James B Mitchell; Gabriel A Rabinovich; Linda J Noble-Haeusslein; Constance M John
Journal:  Cell Transplant       Date:  2010-11-05       Impact factor: 4.064

Review 3.  The Mammalian Blood-Testis Barrier: Its Biology and Regulation.

Authors:  Dolores D Mruk; C Yan Cheng
Journal:  Endocr Rev       Date:  2015-09-10       Impact factor: 19.871

4.  Crosstalk between desmoglein-2/desmocollin-2/Src kinase and coxsackie and adenovirus receptor/ZO-1 protein complexes, regulates blood-testis barrier dynamics.

Authors:  Pearl P Y Lie; C Yan Cheng; Dolores D Mruk
Journal:  Int J Biochem Cell Biol       Date:  2010-02-25       Impact factor: 5.085

Review 5.  The role of actin and myosin during spermatogenesis.

Authors:  Xiao Sun; Tamas Kovacs; Yan-Jun Hu; Wan-Xi Yang
Journal:  Mol Biol Rep       Date:  2010-11-24       Impact factor: 2.316

6.  Unexpected role of α-fetoprotein in spermatogenesis.

Authors:  Futoshi Yazama; Akihiro Tai
Journal:  PLoS One       Date:  2011-05-04       Impact factor: 3.240

7.  Malfunction of spermatogenesis in experimental ischemic mice.

Authors:  Futoshi Yazama; Haruki Sato; Tomoko Sonoda
Journal:  J Reprod Dev       Date:  2015-06-09       Impact factor: 2.214

  7 in total

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