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Planar cell polarity (PCP) proteins support spermatogenesis through cytoskeletal organization in the testis

期刊

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
卷 121, 期 -, 页码 99-113

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2021.04.008

关键词

Testis; Spermatogenesis; PCP proteins; Sertoli cells; Cytoskeletons; F-actin; Microtubules

资金

  1. National Key Research and Development Program of China [2018YFC1003500]
  2. National Natural Science Foundation of China (NSFC) [81971367]
  3. Wenzhou Science & Technology Bureau [Y20190015]
  4. China Shenzhen Science Technology and Innovative Commission (SZSTI) [SZSTIJCYJ20180508152336419]
  5. Second Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University
  6. China Pharmaceutical University World Explorer Study Abroad Scholarship

向作者/读者索取更多资源

This article summarizes the research progress on the role of planar cell polarity (PCP) in supporting spermatogenesis in the testis. Recent studies have shown that PCP proteins in Sertoli cells regulate spermatogenesis by changing the organization of actin and microtubule cytoskeletons. These findings highlight the importance of PCP in supporting spermatogenesis and suggest key areas for future research.
Few reports are found in the literature regarding the role of planar cell polarity (PCP) in supporting sper-matogenesis in the testis. Yet morphological studies reported decades earlier have illustrated the directional alignment of polarized developing spermatids, most notably step 17-19 spermatids in stage V-early VIII tubules in the testis, across the plane of the epithelium in seminiferous tubules of adult rats. Such morphological features have unequivocally demonstrated the presence of PCP in developing spermatids, analogous to the PCP noted in hair cells of the cochlea in mammals. Emerging evidence in recent years has shown that Sertoli and germ cells express numerous PCP proteins, mostly notably, the core PCP proteins, PCP effectors and PCP signaling proteins. In this review, we discuss recent findings in the field regarding the two core PCP protein complexes, namely the Van Gogh-like 2 (Vangl2)/Prickle (Pk) complex and the Frizzled (Fzd)/Dishevelled (Dvl) complex. These findings have illustrated that these PCP proteins exert their regulatory role to support spermatogenesis through changes in the organization of actin and microtubule (MT) cytoskeletons in Sertoli cells. For instance, these PCP proteins confer PCP to developing spermatids. As such, developing haploid spermatids can be aligned and orderly packed within the limited space of the seminiferous tubules in the testes for the production of sperm via spermato-genesis. Thus, each adult male in the mouse, rat or human can produce an upward of 30, 50 or 300 million spermatozoa on a daily basis, respectively, throughout the adulthood. We also highlight critical areas of research that deserve attention in future studies. We also provide a hypothetical model by which PCP proteins support spermatogenesis based on recent studies in the testis. It is conceivable that the hypothetical model shown here will be updated as more data become available in future years, but this information can serve as the framework by investigators to unravel the role of PCP in spermatogenesis.

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