4.5 Article

KIF15 supports spermatogenesis via its effects on Sertoli cell microtubule, actin, vimentin, and septin cytoskeletons

Journal

ENDOCRINOLOGY
Volume 162, Issue 4, Pages -

Publisher

ENDOCRINE SOC
DOI: 10.1210/endocr/bqab010

Keywords

testis; spermatogenesis; microtubule; cytoskeleton; microtubule-dependent motor protein; KIF15; Sertoli cells; blood-testis barrier; cargo transport; spermatid transport

Funding

  1. Eunice Shriver National Institute of Child Health and Human Development [R01 HD056034]
  2. National Key Research and Development Program of China [2018YFC1003500]
  3. National Natural Science Foundation of China (NSFC) [81971367, 81730042]
  4. China Shenzhen Science Technology and Innovative Commission (SZSTI) [SZSTI-JCYJ20180508152336419]
  5. Second Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University

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This study investigated the role of MT-dependent and microtubule plus end-directed motor protein kinesin 15 (KIF15) in the testis. KIF15 showed stage-specific expression and association with MTs in the seminiferous epithelium, playing a crucial role in supporting spermatid transport. Knockdown of KIF15 in Sertoli cells disrupted the barrier function and cytoskeletal organization, indicating that KIF15 regulates cellular functions beyond microtubules.
Throughout spermatogenesis, cellular cargoes including haploid spermatids are required to be transported across the seminiferous epithelium, either toward the microtubule (MT) plus (+) end near the basement membrane at stage V, or to the MT minus (-) end near the tubule lumen at stages VI to VIII of the epithelial cycle. Furthermore, preleptotene spermatocytes, differentiated from type B spermatogonia, are transported across the Sertoli cell blood-testis barrier (BTB) to enter the adluminal compartment. Few studies, however, have been conducted to explore the function of MT-dependent motor proteins to support spermatid transport during spermiogenesis. Herein, we examined the role of MT-dependent and microtubule plus (+) end-directed motor protein kinesin 15 (KIF15) in the testis. KIF15 displayed a stage-specific expression across the seminiferous epithelium, associated with MTs, and appeared as aggregates on the MT tracks that aligned perpendicular to the basement membrane and laid across the entire epithelium. KIF15 also tightly associated with apical ectoplasmic specialization, displaying strict stage-specific distribution, apparently to support spermatid transport across the epithelium. We used a loss-of-function approach by RNAi to examine the role of KIF15 in Sertoli cell epithelium in vitro to examine its role in cytoskeletal-dependent Sertoli cell function. It was noted that KIF15 knockdown by RNAi that reduced KIF15 expression by similar to 70% in Sertoli cells with an established functional tight junction barrier impeded the barrier function.This effect was mediated through remarkable changes in the cytoskeletal organization of MTs, but also actin-, vimentin-, and septin-based cytoskeletons, illustrating that KIF15 exerts its regulatory effects well beyond microtubules.

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