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Reproduction (2008) 135 867-877
DOI: 10.1530/REP-07-0572
Copyright © 2008 Society for Reproduction and Fertility
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RESEARCH

Regulation of testicular tight junctions by gonadotrophins in the adult Djungarian hamster in vivo

Gerard A Tarulli1,2, Sarah J Meachem1,2, Stefan Schlatt3 and Peter G Stanton1

1 Prince Henry's Institute of Medical Research, PO Box 5152, Clayton, Victoria 3168, Australia2 Department of Anatomy and Developmental Biology, Monash University, Clayton, Victoria 3168, Australia and3 Department of Cell Biology and Physiology, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA

Correspondence should be addressed to P G Stanton; Email: peter.stanton{at}princehenrys.org

This study aimed to assess the effect of gonadotrophin suppression and FSH replacement on testicular tight junction dynamics and blood–testis barrier (BTB) organisation in vivo, utilising the seasonal breeding Djungarian hamster. Confocal immunohistology was used to assess the cellular organisation of tight junction proteins and real-time PCR to quantify tight junction mRNA. The effect of tight junction protein organisation on the BTB permeability was also investigated using a biotin-linked tracer. Tight junction protein (claudin-3, junctional adhesion molecule (JAM)-A and occludin) localisation was present but disorganised after gonadotrophin suppression, while mRNA levels (claudin-11, claudin-3 and occludin) were significantly (two- to threefold) increased. By contrast, both protein localisation and mRNA levels for the adaptor protein zona occludens-1 decreased after gonadotrophin suppression. FSH replacement induced a rapid reorganisation of tight junction protein localisation. The functionality of the BTB (as inferred by biotin tracer permeation) was found to be strongly associated with the organisation and localisation of claudin-11. Surprisingly, JAM-A was also recognised on spermatogonia, suggesting an additional novel role for this protein in trans-epithelial migration of germ cells across the BTB. It is concluded that gonadotrophin regulation of tight junction proteins forming the BTB occurs primarily at the level of protein organisation and not gene transcription in this species, and that immunolocalisation of the organised tight junction protein claudin-11 correlates with BTB functionality.







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