4.5 Article

Basement Membrane Laminin α2 Regulation of BTB Dynamics via Its Effects on F-Actin and Microtubule Cytoskeletons Is Mediated Through mTORC1 Signaling

Journal

ENDOCRINOLOGY
Volume 158, Issue 4, Pages 963-978

Publisher

ENDOCRINE SOC
DOI: 10.1210/en.2016-1630

Keywords

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Funding

  1. National Institutes of Health, NICHD [R01 HD056034, U54 HD029990]
  2. Hong Kong Research Grants Council (RGC) [GRF774213, GRF17100816]
  3. RGC/National Natural Science Foundation of China Joint Research Scheme [N_HKU 717/12]
  4. Hong Kong University

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A local axis connects the apical ectoplasmic specialization (ES) at the Sertoli-spermatid interface, the basal ES at the blood-testis barrier (BTB), and the basement membrane across the seminiferous epithelium functionally in rat testes. As such, cellular events that take place simultaneously across the epithelium such as spermiation and BTB remodeling that occur at the apical ES and the basal ES, respectively, at stage VIII of the cycle are coordinated. Herein, laminin alpha 2, a structural component of the basement membrane, was found to regulate BTB dynamics. Sertoli cells were cultured in vitro to allow the establishment of a tight junction (TJ) barrier that mimicked the BTB in vivo. Knockdown of laminin alpha 2 by transfecting Sertoli cells with laminin alpha 2-specific short hairpin RNA vs the nontargeting negative control was shown to perturb the Sertoli cell TJ barrier, illustrating laminin alpha 2 was involved in regulating BTB dynamics. This regulatory effect wasmediated through mammalian target of rapamycin complex 1 (mTORC1) signaling because the two mTORC1 downstream signaling molecules ribosomal protein S6 and Akt1/2 were activated and inactivated, respectively, consistent with earlier findings that mTORC1 is involved in promoting BTB remodeling. Also, laminin alpha 2 knockdown induced F-actin and microtubule (MT) disorganization through changes in the spatial expression of F-actin regulators actin-related protein 3 and epidermal growth factor receptor pathway substrate 8 vs end-binding protein 1 (a MT plus-end tracking protein, +TIP). These laminin alpha 2 knockdown-mediated effects on F-actin and MT organization was blocked by exposing Sertoli cells to rapamycin, an inhibitor of mTORC1 signaling, and also SC79, an activator of Akt. In summary, laminin alpha 2-mediated regulation on Sertoli cell BTB dynamics is through mTORC1 signaling.

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