Sertoli cell–specific coxsackievirus and adenovirus receptor regulates cell adhesion and gene transcription via β‐catenin inactivation and Cdc42 activation. Issue 6 (20th March 2019)
- Record Type:
- Journal Article
- Title:
- Sertoli cell–specific coxsackievirus and adenovirus receptor regulates cell adhesion and gene transcription via β‐catenin inactivation and Cdc42 activation. Issue 6 (20th March 2019)
- Main Title:
- Sertoli cell–specific coxsackievirus and adenovirus receptor regulates cell adhesion and gene transcription via β‐catenin inactivation and Cdc42 activation
- Authors:
- Huang, Kun
Ru, Beibei
Zhang, Yang
Chan, Wai-Lung
Chow, Sheung-Ching
Zhang, Jiangwen
Lo, Clive
Lui, Wing-Yee - Abstract:
- ABSTRACT: Blood‐testis barrier (BTB) and apical ectoplasmic specialization (ES) serve as structural supports for germ cell (GC) development. We demonstrated that the Sertoli cell (SC)‐specific coxsackievirus and adenovirus receptor (CXADR) knockout (SC‐CXADR −/− ), but not the GC‐specific knockout, impaired spermatogenesis. An increase in GC apoptosis and premature loss of elongated spermatids were observed in SC‐CXADR −/− testes. The BTB function was compromised in SC‐CXADR −/− testes with dysregulation of oocludin and zonula occludens‐1 expression at the basal compartment of the seminiferous epithelium. An integrated omics analyses confirmed that altered gene ontology terms identified in SC‐CXADR −/− testes are highly associated with spermatid development and differentiation, spermatogenesis, and sperm motility and are considered as unique testicular function terms. Leptin, Nasp, Tektin3, Larp 7, and acrosin, which are highly associated with male fertility, were found to be down‐regulated in SC‐CXADR −/− testes. Based on the data from the omics analyses, we employed the CXADR‐deficient SC model to further investigate the molecular mechanisms involved. We unraveled that SC‐CXADRs are required for β‐catenin inactivation and cell division cycle protein 42 (Cdc42) activation, resulting in maintaining the integrity and function of the BTB and apical ES as well as inhibiting gene transcription, such as the Myc gene, in the testes. We demonstrated for the first time that CXADR isABSTRACT: Blood‐testis barrier (BTB) and apical ectoplasmic specialization (ES) serve as structural supports for germ cell (GC) development. We demonstrated that the Sertoli cell (SC)‐specific coxsackievirus and adenovirus receptor (CXADR) knockout (SC‐CXADR −/− ), but not the GC‐specific knockout, impaired spermatogenesis. An increase in GC apoptosis and premature loss of elongated spermatids were observed in SC‐CXADR −/− testes. The BTB function was compromised in SC‐CXADR −/− testes with dysregulation of oocludin and zonula occludens‐1 expression at the basal compartment of the seminiferous epithelium. An integrated omics analyses confirmed that altered gene ontology terms identified in SC‐CXADR −/− testes are highly associated with spermatid development and differentiation, spermatogenesis, and sperm motility and are considered as unique testicular function terms. Leptin, Nasp, Tektin3, Larp 7, and acrosin, which are highly associated with male fertility, were found to be down‐regulated in SC‐CXADR −/− testes. Based on the data from the omics analyses, we employed the CXADR‐deficient SC model to further investigate the molecular mechanisms involved. We unraveled that SC‐CXADRs are required for β‐catenin inactivation and cell division cycle protein 42 (Cdc42) activation, resulting in maintaining the integrity and function of the BTB and apical ES as well as inhibiting gene transcription, such as the Myc gene, in the testes. We demonstrated for the first time that CXADR is an important mediator governing β‐catenin and Cdc42 signaling that is essential for spermatogenesis. The molecular mechanisms identified herein may provide new insights to unravel the novel functions and signaling cascades of CXADR in other key CXADR‐expressing tissues.—Huang, K., Ru, B., Zhang, Y., Chan, W.‐L., Chow, S.‐C., Zhang, J., Lo, C., Lui, W.‐Y. Sertoli cell‐specific coxsackievirus and adenovirus receptor regulates cell adhesion and gene transcription via β‐catenin inactivation and Cdc42 activation. FASEB J. 33, 7588–7602 (2019). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 33:Issue 6(2019)
- Journal:
- FASEB journal
- Issue:
- Volume 33:Issue 6(2019)
- Issue Display:
- Volume 33, Issue 6 (2019)
- Year:
- 2019
- Volume:
- 33
- Issue:
- 6
- Issue Sort Value:
- 2019-0033-0006-0000
- Page Start:
- 7588
- Page End:
- 7602
- Publication Date:
- 2019-03-20
- Subjects:
- blood–testis barrier -- ectoplasmic specialization -- reproductive impairment -- spermatogenesis
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201801584R ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13232.xml