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Regulation of spermatogenesis by a local functional axis in the testis: role of the basement membrane-derived noncollagenous 1 domain peptide.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2017

Spermatogenesis takes place in the epithelium of the seminiferous tubules of the testes, producing millions of spermatozoa per day in an adult male in rodents and humans. Thus, multiple cellular events that are regulated by an array of signaling molecules and pathways are tightly coordinated to support spermatogenesis. Here, we report findings of a local regulatory axis between the basement membrane (BM), the blood-testis barrier (BTB), and the apical ectoplasmic specialization (apical ES; a testis-specific, actin-rich adherens junction at the Sertoli cell-spermatid interface) to coordinate cellular events across the seminiferous epithelium during the epithelial cycle. In short, a biologically active fragment, noncollagenous 1 (NC1) domain that is derived from collagen chains in the BM, was found to modulate cell junction dynamics at the BTB and apical ES. NC1 domain from the collagen α3(IV) chain was cloned into a mammalian expression vector, pCI-neo, with and without a collagen signal peptide. We also prepared a specific Ab against the purified recombinant NC1 domain peptide. These reagents were used to examine whether overexpression of NC1 domain with high transfection efficacy would perturb spermatogenesis, in particular, spermatid adhesion (i.e., inducing apical ES degeneration) and BTB function (i.e., basal ES and tight junction disruption, making the barrier leaky), in the testis in vivo We report our findings that NC1 domain derived from collagen α3(IV) chain-a major structural component of the BM-was capable of inducing BTB remodeling, making the BTB leaky in studies in vivo Furthermore, NC1 domain peptide was transported across the epithelium via a microtubule-dependent mechanism and is capable of inducing apical ES degeneration, which leads to germ cell exfoliation from the seminiferous epithelium. Of more importance, we show that NC1 domain peptide exerted its regulatory effect by disorganizing actin microfilaments and microtubules in Sertoli cells so that they failed to support cell adhesion and transport of germ cells and organelles (e.g., residual bodies, phagosomes) across the seminiferous epithelium. This local regulatory axis between the BM, BTB, and the apical ES thus coordinates cellular events that take place across the seminiferous epithelium during the epithelial cycle of spermatogenesis.-Chen, H., Mruk, D. D., Lee, W. M., Cheng, C. Y. Regulation of spermatogenesis by a local functional axis in the testis: role of the basement membrane-derived noncollagenous 1 domain peptide.

Pubmed ID: 28487282 RIS Download

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Associated grants

  • Agency: NICHD NIH HHS, United States
    Id: R01 HD056034
  • Agency: NICHD NIH HHS, United States
    Id: U54 HD029990

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

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alpha Tubulin antibody [DM1A] - Loading Control (antibody)

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Nectin 2 (C-15) (antibody)

RRID:AB_2174166

This polyclonal targets PVRL2

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N-cadherin Monoclonal Antibody (3B9) (antibody)

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Eps8 (antibody)

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COL4A3 (T-15) (antibody)

RRID:AB_2082655

This polyclonal targets COL4A3

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Claudin 11 Polyclonal Antibody (antibody)

RRID:AB_2533259

This unknown targets Claudin 11

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CAR (N-17) (antibody)

RRID:AB_2261263

This polyclonal targets CXADR

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CAR (H-300) (antibody)

RRID:AB_2087557

This polyclonal targets CXADR

View all literature mentions

Integrin beta1 (N-20) (antibody)

RRID:AB_2128200

This polyclonal targets ITGB1

View all literature mentions

alpha Tubulin antibody [DM1A] - Loading Control (antibody)

RRID:AB_2241126

This monoclonal targets alpha Tubulin antibody [DM1A] - Loading Control

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Goat Anti-Actin Polyclonal antibody, Unconjugated (antibody)

RRID:AB_630836

This polyclonal targets ACTG1, ACTC1, ACTA1, ACTA2, ACTG2, ACTB

View all literature mentions