The interconnection between cytokeratin and cell membrane-bound β-catenin in Sertoli cells derived from juvenile Xenopus tropicalis testes
Status PubMed-not-MEDLINE Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články
PubMed
31822471
PubMed Central
PMC6955214
DOI
10.1242/bio.043950
PII: bio.043950
Knihovny.cz E-zdroje
- Klíčová slova
- Adherens junctions, Cytokeratin, Immature Sertoli cells, Testicles, Xenopus tropicalis,
- Publikační typ
- časopisecké články MeSH
Sertoli cells (SCs) play a central role in the determination of male sex during embryogenesis and spermatogenesis in adulthood. Failure in SC development is responsible for male sterility and testicular cancer. Before the onset of puberty, SCs are immature and differ considerably from mature cells in post-pubertal individuals regarding their morphology and biochemical activity. The major intermediate filament (IF) in mature SCs is vimentin, anchoring germ cells to the seminiferous epithelium. The collapse of vimentin has resulted in the disintegration of seminiferous epithelium and subsequent germ cell apoptosis. However, another IF, cytokeratin (CK) is observed only transiently in immature SCs in many species. Nevertheless, its function in SC differentiation is poorly understood. We examined the interconnection between CK and cell junctions using membrane β-catenin as a marker during testicular development in the Xenopus tropicalis model. Immunohistochemistry on juvenile (5 months old) testes revealed co-expression of CK, membrane β-catenin and E-cadherin. Adult (3-year-old males) samples confirmed only E-cadherin expression; CK and β-catenin were lost. To study the interconnection between CK and β-catenin-based cell junctions, the culture of immature SCs (here called XtiSCs) was employed. Suppression of CK by acrylamide in XtiSCs led to breakdown of membrane-bound β-catenin but not F-actin and β-tubulin or cell-adhesion proteins (focal adhesion kinase and integrin β1). In contrast to the obvious dependence of membrane β-catenin on CK stability, the detachment of β-catenin from the plasma membrane via uncoupling of cadherins by Ca2+ chelator EGTA had no effect on CK integrity. Interestingly, CHIR99021, a GSK3 inhibitor, also suppressed the CK network, resulting in the inhibition of XtiSCs cell-to-cell contacts and testicular development in juvenile frogs. This study suggests a novel role of CK in the retention of β-catenin-based junctions in immature SCs, and thus provides structural support for seminiferous tubule formation and germ cell development.
Zobrazit více v PubMed
Ameen N. A., Figueroa Y. and Salas P. J. (2001). Anomalous apical plasma membrane phenotype in CK8-deficient mice indicates a novel role for intermediate filaments in the polarization of simple epithelia. PubMed
Appert A., Fridmacher V., Locquet O. and Magre S. (1998). Patterns of keratins 8, 18 and 19 during gonadal differentiation in the mouse: sex- and time-dependent expression of keratin 19. PubMed DOI
Barrionuevo F., Burgos M. and Jiménez R. (2011). Origin and function of embryonic Sertoli cells. PubMed DOI
Bhattacharjee R., Goswami S., Dudiki T., Popkie A. P., Phiel C. J., Kline D. and Vijayaraghavan S. (2015). Targeted disruption of glycogen synthase kinase 3A (GSK3A) in mice affects sperm motility resulting in male infertility. PubMed DOI PMC
Bilic J., Huang Y. L., Davidson G., Zimmermann T., Cruciat C. M., Bienz M. and Niehrs C. (2007). Wnt induces LRP6 signalosomes and promotes dishevelled-dependent LRP6 phosphorylation. PubMed DOI
Chairoungdua A., Smith D. L., Pochard P., Hull M. and Caplan M. J. (2010). Exosome release of β-catenin: a novel mechanism that antagonizes Wnt signaling. PubMed DOI PMC
Chen E. Y., DeRan M. T., Ignatius M. S., Grandinetti K. B., Clagg R., McCarthy K. M., Lobbardi R. M., Brockmann J., Keller C., Wu X. et al. (2014). Glycogen synthase kinase 3 inhibitors induce the canonical WNT/β-catenin pathway to suppress growth and self-renewal in embryonal rhabdomyosarcoma. PubMed DOI PMC
Daugherty R. L. and Gottardi C. J. (2007). Phospho-regulation of β-Catenin adhesion and signaling functions. PubMed DOI PMC
de Winter J. P., Vanderstichele H. M., Timmerman M. A., Blok L. J., Themmen A. P. and de Jong F. H. (1993). Activin is produced by rat Sertoli cells in vitro and can act as an autocrine regulator of Sertoli cell function. PubMed DOI
Duncan A. R., Forcina J. J., Tsang P. C. W. and Townson D. H. (2009). Disruption of cytokeratin 18-containing intermediate filaments in bovine luteal cells: effects of acrylamide on progesterone secretion, fas expression, and FasL-induced apoptosis. DOI
Engl W., Arasi B., Yap L. L., Thiery J. P. and Viasnoff V. (2014). Actin dynamics modulate mechanosensitive immobilization of E-cadherin at adherens junctions. PubMed DOI
Fagotto F., Funayama N., Gluck U. and Gumbiner B. M. (1996). Binding to cadherins antagonizes the signaling activity of beta-catenin during axis formation in Xenopus. PubMed DOI PMC
Francipane M. G. and Lagasse E. (2015). The lymph node as a new site for kidney organogenesis. PubMed DOI PMC
García-Reyes B., Witt L., Jansen B., Karasu E., Gehring T., Leban J., Henne-Bruns D., Pichlo C., Brunstein E., Baumann U. et al. (2018). Discovery of inhibitor of wnt production 2 (IWP-2) and related compounds as selective ATP-competitive inhibitors of casein kinase 1 (CK1) δ/ε. PubMed DOI
Geach T. J. and Zimmerman L. B. (2011). Developmental genetics in Xenopus tropicalis. PubMed DOI
Hanada S., Harada M., Kumemura H., Omary M. B., Kawaguchi T., Taniguchi E., Koga H., Yoshida T., Maeyama M., Baba S. et al. (2005). Keratin-containing inclusions affect cell morphology and distribution of cytosolic cellular components. PubMed DOI
Handelsman D. J., Spaliviero J. A. and Phippard A. F. (1990). Highly vectorial secretion of inhibin by primate sertoli cellsin vitro*. PubMed DOI
Hartsock A. and Nelson W. J. (2008). Adherens and tight junctions: structure, function and connections to the actin cytoskeleton. PubMed DOI PMC
Heasman J., Crawford A., Goldstone K., Garner-Hamrick P., Gumbiner B., McCrea P., Kintner C., Noro C. Y. and Wylie C. (1994). Overexpression of cadherins and underexpression of beta-catenin inhibit dorsal mesoderm induction in early Xenopus embryos. PubMed DOI
Huber A. H. and Weis W. I. (2001). The structure of the β-catenin/E-cadherin complex and the molecular basis of diverse ligand recognition by β-catenin. PubMed DOI
Johnson M., Sharma M., Jamieson C., Henderson J. M., Mok M. T. S., Bendall L. and Henderson B. R. (2009). Regulation of β-catenin trafficking to the membrane in living cells. PubMed DOI
Kaufhold S. and Bonavida B. (2014). Central role of Snail1 in the regulation of EMT and resistance in cancer: a target for therapeutic intervention. PubMed DOI PMC
Kramer T., Schmidt B. and Lo Monte F. (2012). Small-molecule inhibitors of GSK-3: structural insights and their application to alzheimer's disease models. PubMed DOI PMC
Ku N. O. and Omary M. B. (1997). Phosphorylation of human keratin 8 in vivo at conserved head domain serine 23 and at epidermal growth factor-stimulated tail domain serine 431. PubMed DOI
Lee C.-H. and Taketo T. (1994). Normal onset, but prolonged expression, of Sry gene in the B6.YDOM sex-reversed mouse gonad. PubMed DOI
Makarova G., Bette M., Schmidt A., Jacob R., Cai C., Rodepeter F., Betz T., Sitterberg J., Bakowsky U., Moll R. et al. (2013). Epidermal growth factor-induced modulation of cytokeratin expression levels influences the morphological phenotype of head and neck squamous cell carcinoma cells. PubMed DOI
Mital P., Kaur G. and Dufour J. M. (2010). Immunoprotective sertoli cells: making allogeneic and xenogeneic transplantation feasible. PubMed DOI
Myers M., Ebling F. J. P., Nwagwu M., Boulton R., Wadhwa K., Stewart J. and Kerr J. B. (2005). Atypical development of Sertoli cells and impairment of spermatogenesis in the hypogonadal (hpg) mouse. PubMed DOI PMC
Nazarian H., Ghaffari Novin M., Jalili M. R., Mirfakhraie R., Heidari M. H., Hosseini S. J., Norouzian M. and Ehsani N. (2014). Expression of Glycogen synthase kinase 3-β (GSK3-β) gene in azoospermic men. PubMed PMC
Nguyen T. M. X., Vegrichtova M., Tlapakova T., Krulova M. and Krylov V. (2019). Epithelial-mesenchymal transition promotes the differentiation potential of Xenopus tropicalis immature Sertoli cells. PubMed DOI PMC
Nistal M., Paniagua R., Abaurrea M. A. and Santamaría L. (1982). Hyperplasia and the immature appearance of Sertoli cells in primary testicular disorders. PubMed DOI
Pachenari N., Kiani S. and Javan M. (2017). Inhibition of glycogen synthase kinase 3 increased subventricular zone stem cells proliferation. PubMed DOI
Paranko J., Kallajoki M., Pelliniemi L. J., Lehto V.-P. and Virtanen I. (1986). Transient coexpression of cytokeratin and vimentin in differentiating rat Sertoli cells. PubMed DOI
Petrosyan A., Ali M. F. and Cheng P.-W. (2015). Keratin 1 plays a critical role in golgi localization of core 2 PubMed DOI PMC
Potokar M., Kreft M., Li L., Daniel Andersson J., Pangršič T., Chowdhury H. H., Pekny M. and Zorec R. (2007). Cytoskeleton and vesicle mobility in astrocytes. PubMed DOI
Rogatsch H., Hittmair A., Mikuz G., Feichtinger H. and Jezek D. (1996). Expression of vimentin, cytokeratin, and desmin in Sertoli cells of human fetal, cryptorchid, and tumour-adjacent testicular tissue. PubMed DOI
Setchell B. P. (2009). Blood-testis barrier, junctional and transport proteins and spermatogenesis. PubMed DOI
Shabana A. H. M., Oboeuf M. and Forest N. (1994). Cytoplasmic desmosomes and intermediate filament disturbance following acrylamide treatment in cultured rat keratinocytes. PubMed DOI
Sharpe R. M., McKinnell C., Kivlin C. and Fisher J. S. (2003). Proliferation and functional maturation of Sertoli cells, and their relevance to disorders of testis function in adulthood. PubMed DOI
Smaill J. B., Palmer B. D., Rewcastle G. W., Denny W. A., McNamara D. J., Dobrusin E. M., Bridges A. J., Zhou H., Showalter H. D., Winters R. T. et al. (1999). Tyrosine kinase inhibitors. 15. 4-(Phenylamino)quinazoline and 4-(phenylamino)pyrido[d]pyrimidine acrylamides as irreversible inhibitors of the ATP binding site of the epidermal growth factor receptor. PubMed DOI
Sonavane P. R., Wang C., Dzamba B., Weber G. F., Periasamy A. and DeSimone D. W. (2017). Mechanical and signaling roles for keratin intermediate filaments in the assembly and morphogenesis of Xenopus mesendoderm tissue at gastrulation. PubMed DOI PMC
Steinberger A. and Steinberger E. (1971). Replication pattern of Sertoli cells in maturing rat testis in vivo and in organ culture. PubMed DOI
Stosiek P., Kasper M. and Karsten U. (1990). Expression of cytokeratins 8 and 18 in human Sertoli cells of immature and atrophic seminiferous tubules. PubMed DOI
Tlapakova T., Nguyen T. M. X., Vegrichtova M., Sidova M., Strnadova K., Blahova M. and Krylov V. (2016). Identification and characterization of Xenopus tropicalis common progenitors of Sertoli and peritubular myoid cell lineages. PubMed DOI PMC
Towbin H., Staehelin T. and Gordon J. (1992). Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. 1979. PubMed
Vijayaraj P., Kröger C., Reuter U., Windoffer R., Leube R. E. and Magin T. M. (2009). Keratins regulate protein biosynthesis through localization of GLUT1 and -3 upstream of AMP kinase and Raptor. PubMed DOI PMC
Wahab-Wahlgren A., Holst M., Ayele D., Sultana T., Parvinen M., Gustafsson K., Granholm T. and Söder O. (2000). Constitutive production of interleukin-1alpha mRNA and protein in the developing rat testis. PubMed DOI
Wen Q., Tang E. I., Xiao X., Gao Y., Chu D. S., Mruk D. D., Silvestrini B. and Cheng C. Y. (2016). Transport of germ cells across the seminiferous epithelium during spermatogenesis-the involvement of both actin- and microtubule-based cytoskeletons. PubMed DOI PMC
Wolski K. M., Perrault C., Tran-Son-Tay R. and Cameron D. F. (2005). Strength measurement of the Sertoli-spermatid junctional complex. PubMed DOI
Wu K., Fan J., Zhang L., Ning Z., Zeng J., Zhou J., Li L., Chen Y., Zhang T., Wang X. et al. (2012). PI3K/Akt to GSK3β/β-catenin signaling cascade coordinates cell colonization for bladder cancer bone metastasis through regulating ZEB1 transcription. PubMed DOI
Wu S. K., Gomez G. A., Michael M., Verma S., Cox H. L., Lefevre J. G., Parton R. G., Hamilton N. A., Neufeld Z. and Yap A. S. (2014). Cortical F-actin stabilization generates apical–lateral patterns of junctional contractility that integrate cells into epithelia. PubMed DOI
Yoshida T., Sopko N. A., Kates M., Liu X., Joice G., McConkey D. J. and Bivalacqua T. J. (2018). Three-dimensional organoid culture reveals involvement of Wnt/β-catenin pathway in proliferation of bladder cancer cells. PubMed DOI PMC