scholarly journals Osteopontin and related SIBLING glycoprotein genes are expressed by Sertoli cells during mouse testis development

2005 ◽  
Vol 233 (4) ◽  
pp. 1488-1495 ◽  
Author(s):  
Megan J. Wilson ◽  
Lucy Liaw ◽  
Peter Koopman
Keyword(s):  
Sertoli Cells ◽  
Mouse Testis ◽  
Testis Development

232. Developmentally regulated activin A signal transduction by Sertoli cells is required for normal mouse testis development

2008 ◽  
Vol 20 (9) ◽  
pp. 32
Author(s):  
C. M. Itman ◽  
C. Small ◽  
M. Griswold ◽  
A. K. Nagaraja ◽  
M. M. Matzuk ◽  
...  
Keyword(s):  
Signal Transduction ◽  
Sertoli Cell ◽  
Sertoli Cells ◽  
Normal Mouse ◽  
Mouse Testis ◽  
Nuclear Accumulation ◽  
Developmentally Regulated ◽  
Testis Development ◽  
Differentiated Cells ◽  
Immature Cells

Activin A, a TGF-β superfamily ligand, is critical for normal mouse testis development and quantitatively normal sperm production. Testicular activin production changes during development, being substantially higher in the immature testis relative to the adult [1, 2]. Activin influences the Sertoli cell, the nurse cell to developing sperm, enhancing proliferation during its immature phase, but not following terminal differentiation [3]. In the Inha−/− mouse, chronic excessive activin production results in Sertoli cell-derived tumours [4] whereas reduced activin bioactivity, in the InhbaBK/BK mouse, delays fertility [5]. Activin signals are transduced by the phosphorylation and nuclear accumulation of the transcription factors SMAD2 and SMAD3. By comparing activin signal transduction in immature v. terminally differentiated Sertoli cells, using quantitative confocal microscopy and western blot analysis of total and phosphorylated SMAD2 and SMAD3, we discovered that mouse Sertoli cells exhibit developmentally regulated activin responses. Activin induces nuclear accumulation of SMAD3, but not SMAD2, in immature cells, although both proteins are phosphorylated. In contrast, terminally differentiated cells exhibit nuclear accumulation of both SMAD2 and SMAD3. We observed that this shift coincides with decreased SMAD3 production at puberty and changes in FSH-induced Smad transcription, which favours Smad3 in immature cells but promotes Smad2 synthesis in terminally differentiated cells. Furthermore, whereas removal of SMAD3 from the Inha−/− mouse rescues the tumour phenotype [6], we demonstrated that insufficient SMAD3 production impairs testis growth. We hypothesised that this developmentally regulated SMAD utilisation drives specific transcriptional outcomes. Using microarray and quantitative PCR, we identified novel activin target genes displaying developmental stage-specific expression patterns coinciding with differential SMAD usage, including Gja1 and Serpina5 which are required for male fertility. These mRNAs are also modulated in vivo, increased 1.5–2 fold in Inha−/− testes and decreased by half in InhbaBK/BK testes, confirming that normal testis development requires carefully regulated activin production and responsiveness. (1) Buzzard J et al. 2004. Endocrinology 145(7): 3532–3541 (2) Barakat et al. 2008. Reproduction 2008 Epub ahead of print (3) Boitani C et al. 1995. Endocrinology 136(12): 4538–4544 (4) Matzuk M et al. 1992. Nature 360: 313–319 (5) Brown C et al. 2000. Nature Genetics 25(4): 453–457 (6) Li Q et al. 2007. Molecular Endocrinology 21(10: 2472–2486

Development of Testis Cords and the Formation of Efferent Ducts in Xenopus laevis: Differences and Similarities with Other Vertebrates

2021 ◽  
pp. 1-14
Author(s):  
Yuanyuan Li ◽  
Jinbo Li ◽  
Man Cai ◽  
Zhanfen Qin
Keyword(s):  
Cell Proliferation ◽  
Xenopus Laevis ◽  
Germ Cells ◽  
Sertoli Cells ◽  
Testis Development ◽  
Larval Stages ◽  
Efferent Ducts ◽  
Steroidogenic Cells ◽  
Testis Cord ◽  
Anterior Posterior

The knowledge of testis development in amphibians relative to amniotes remains limited. Here, we used Xenopus laevis to investigate the process of testis cord development. Morphological observations revealed the presence of segmental gonomeres consisting of medullary knots in male gonads at stages 52–53, with no distinct gonomeres in female gonads. Further observations showed that cell proliferation occurs at specific sites along the anterior-posterior axis of the future testis at stage 50, which contributes to the formation of medullary knots. At stage 53, adjacent gonomeres become close to each other, resulting in fusion; then (pre-)Sertoli cells aggregate and form primitive testis cords, which ultimately become testis cords when germ cells are present inside. The process of testis cord formation in X. laevis appears to be more complex than in amniotes. Strikingly, steroidogenic cells appear earlier than (pre-)Sertoli cells in differentiating testes of X. laevis, which differs from earlier differentiation of (pre-)Sertoli cells in amniotes. Importantly, we found that the mesonephros is connected to the testis gonomere at a specific site at early larval stages and that these connections become efferent ducts after metamorphosis, which challenges the previous concept that the mesonephric side and the gonadal side initially develop in isolation and then connect to each other in amphibians and amniotes.

Developmental stage- and spermatogenic cycle-specific expression of transcription factor GATA-1 in mouse Sertoli cells

Development ◽  
1994 ◽  
Vol 120 (7) ◽  
pp. 1759-1766 ◽  
Author(s):  
K. Yomogida ◽  
H. Ohtani ◽  
H. Harigae ◽  
E. Ito ◽  
Y. Nishimune ◽  
...  
Keyword(s):  
Transcription Factor ◽  
Developmental Stage ◽  
Sertoli Cell ◽  
Germ Cells ◽  
Sertoli Cells ◽  
Transcriptional Activation ◽  
Germ Line ◽  
Mouse Testis ◽  
Seminiferous Tubules ◽  
Specific Expression

GATA-1 is an essential factor for the transcriptional activation of erythroid-specific genes, and is also abundantly expressed in a discrete subset of cells bordering the seminiferous epithelium in tubules of the murine testis. In examining normal and germ-line defective mutant mice, we show here that GATA-1 is expressed only in the Sertoli cell lineage in mouse testis. GATA-1 expression in Sertoli cells is induced concomitantly with the first wave of spermatogenesis, and GATA-1-positive cells are uniformly distributed among all tubules during prepubertal testis development. However, the number of GATA-1-positive cells declines thereafter and were found only in the peripheral zone of seminiferous tubules in stages VII, VIII and IX of spermatogenesis in the adult mouse testis. In contrast, virtually every Sertoli cell in mutant W/Wv, jsd/jsd or cryptorchid mice (all of which lack significant numbers of germ cells) expresses GATA-1, thus showing that the expression of this transcription factor is negatively controlled by the maturing germ cells. These observations suggest that transcription factor GATA-1 is a developmental stage- and spermatogenic cycle-specific regulator of gene expression in Sertoli cells.

scholarly journals Sertoli Cells Are Susceptible to ZIKV Infection in Mouse Testis

2017 ◽  
Vol 7 ◽  
Author(s):  
Zi-Yang Sheng ◽  
Na Gao ◽  
Zhao-Yang Wang ◽  
Xiao-Yun Cui ◽  
De-Shan Zhou ◽  
...  
Keyword(s):  
Sertoli Cells ◽  
Mouse Testis ◽  
Zikv Infection

scholarly journals Differential expression of glucose transporter GLUT8 during mouse spermatogenesis

Reproduction ◽  
2006 ◽  
Vol 131 (1) ◽  
pp. 63-70 ◽  
Author(s):  
Olga Gómez ◽  
Amparo Romero ◽  
José Terrado ◽  
José E Mesonero
Keyword(s):  
Western Blot ◽  
Differential Expression ◽  
Germ Cells ◽  
Sertoli Cells ◽  
Glucose Transporter ◽  
Mouse Testis ◽  
Pivotal Role ◽  
Interstitial Tissue ◽  
Rt Pcr ◽  
Fuel Supply

GLUT8 is a facilitative glucose transporter expressed at high levels in the testis. In this study, we analyzed the GLUT8 expression in mouse testis during spermatogenesis by RT–PCR, Western blot and immunohistochemistry methods. Our results show that GLUT8 expression is limited to spermatids and spermatozoa in the testis. Expression begins when round spermatids are formed at postnatal day 24. The expression persists throughout spermiogenesis, and it is also detected in spermatozoa, but it is absent in more immature germ cells, Sertoli cells and interstitial tissue. GLUT8 immunoreactivity is always restricted to the acrosomic system in a manner that matches the acrosome system formation. The GLUT8 expression is mainly associated with the acrosomic membrane in the acrosome, although significant immunoreactivity is also found inside the acrosomic lumen. The specific GLUT8 location suggests that this transporter plays a pivotal role in the fuel supply of spermatozoa, and in the traffic of sugars during the capacitation and fertilization processes.

scholarly journals Expression and localization of aromatase during fetal mouse testis development

2013 ◽  
Vol 23 (1) ◽  
pp. 12 ◽  
Author(s):  
Caroline Borday ◽  
Jorge Merlet ◽  
Chrystèle Racine ◽  
René Habert
Keyword(s):  
Mouse Testis ◽  
Fetal Mouse ◽  
Testis Development

scholarly journals Crlz-1 Is Prominently Expressed in Spermatogonia and Sertoli Cells during Early Testis Development and in Spermatids during Late Spermatogenesis

2013 ◽  
Vol 61 (7) ◽  
pp. 522-528 ◽  
Author(s):  
Jung-Hyun Lim ◽  
Seong-Young Choi ◽  
Han-Woong Yoo ◽  
Sun-Jung Cho ◽  
Youngsook Son ◽  
...  
Keyword(s):  
Sertoli Cells ◽  
Testis Development
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