Search Results

You are looking at 1 - 1 of 1 items for

  • Author: Kathrin Gassei x
  • Refine by access: All content x
Clear All Modify Search
Kathrin Gassei Department of Cell Biology and Physiology, Institute of Reproductive and Regenerative Biology, Center for Research in Reproductive Physiology, University of Pittsburgh School of Medicine, 3500 Terrace Street, Pittsburgh, Pennsylvania 15261, USA

Search for other papers by Kathrin Gassei in
Google Scholar
PubMed
Close
,
Jens Ehmcke Department of Cell Biology and Physiology, Institute of Reproductive and Regenerative Biology, Center for Research in Reproductive Physiology, University of Pittsburgh School of Medicine, 3500 Terrace Street, Pittsburgh, Pennsylvania 15261, USA
Department of Cell Biology and Physiology, Institute of Reproductive and Regenerative Biology, Center for Research in Reproductive Physiology, University of Pittsburgh School of Medicine, 3500 Terrace Street, Pittsburgh, Pennsylvania 15261, USA

Search for other papers by Jens Ehmcke in
Google Scholar
PubMed
Close
, and
Stefan Schlatt Department of Cell Biology and Physiology, Institute of Reproductive and Regenerative Biology, Center for Research in Reproductive Physiology, University of Pittsburgh School of Medicine, 3500 Terrace Street, Pittsburgh, Pennsylvania 15261, USA
Department of Cell Biology and Physiology, Institute of Reproductive and Regenerative Biology, Center for Research in Reproductive Physiology, University of Pittsburgh School of Medicine, 3500 Terrace Street, Pittsburgh, Pennsylvania 15261, USA

Search for other papers by Stefan Schlatt in
Google Scholar
PubMed
Close

The first morphological sign of testicular differentiation is the formation of testis cords. Prior to cord formation, newly specified Sertoli cells establish adhesive junctions, and condensation of somatic cells along the surface epithelium of the genital ridge occurs. Here, we show that Sertoli cell aggregation is necessary for subsequent testis cord formation, and that neurotrophic tyrosine kinase receptors (NTRKs) regulate this process. In a three-dimensional cell culture assay, immature rat Sertoli cells aggregate to form large spherical aggregates (81.36±7.34 μm in diameter) in a highly organized, hexagonal arrangement (376.95±21.93 μm average distance between spherical aggregates). Exposure to NTRK inhibitors K252a and AG879 significantly disrupted Sertoli cell aggregation in a dose-dependent manner. Sertoli cells were prevented from establishing cell–cell contacts and from forming spherical aggregates. In vitro-derived spherical aggregates were xenografted into immunodeficient nude mice to investigate their developmental potential. In controls, seminiferous tubule-like structures showing polarized single-layered Sertoli cell epithelia, basement membranes, peritubular myoid cells surrounding the tubules, and lumen were observed in histological sections. By contrast, grafts from treatment groups were devoid of tubules and only few single Sertoli cells were present in xenografts after 4 weeks. Furthermore, the grafts were significantly smaller when Sertoli cell aggregation was disrupted by K252a in vitro (20.87 vs 6.63 mg; P<0.05). We conclude from these results that NTRK-regulated Sertoli–Sertoli cell contact is essential to the period of extensive growth and remodeling that occurs during testicular tubulogenesis, and our data indicate its potential function in fetal and prepubertal testis differentiation.

Free access