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Updated: Sep 27, 2026

Derivation of Mouse Trophoblast Stem Cells from Blastocysts
Published on: June 8, 2010
Receptor tyrosine kinase Ron is expressed in mouse reproductive tissues during embryo implantation and is important
Karla Ann Hess1, Susan E Waltz, Edward L Chan
1Divisions of Developmental Biology, Cincinnati Children's Research Foundation, Cincinnati, Ohio 45229, USA.
Abstract:
Ron is a receptor tyrosine kinase that is activated by the binding of hepatocyte growth factor-like (HGFL) protein. Mutations in the catalytic domain of this receptor result in an aggressively invasive phenotype. Conversely, deletion of the entire receptor results in an embryonic lethality by Embryonic Day 7.5. The specific cellular localization and mechanisms of action of Ron and HGFL during embryo implantation are not known. Therefore, this report characterizes the temporal and spatial distribution of this receptor during mouse embryo implantation and placentation. Reverse transcription-polymerase chain reaction analysis demonstrated the presence of Ron transcripts in the uterus, placenta, testis, and epididymis, whereas HGFL transcripts were found in the cervix, placenta, epididymis, and testis. In situ hybridization and immunohistochemical analyses demonstrated that Ron was present in the cells of the ectoplacental cone and trophoblast giant cell regions surrounding the implanting embryo. Ron expression was also observed in SM9-1, SM9-2, and SM-10 murine trophoblast cell lines. To determine the effects of Ron activation on trophoblast function, Matrigel invasion and cell survival assays were performed using the SM9-1 and SM-10 trophoblast cell lines. The HGFL stimulation of these cells increased invasion and enhanced cell survival. These observations suggest that activation of the Ron receptor by HGFL binding may aid in implantation by way of trophoblast function and viability.
Insights
The Ron receptor and HGFL protein are crucial for mouse embryo implantation. Ron activation by HGFL enhances trophoblast invasion and survival, aiding successful implantation and placentation.
Area of Science:
- Developmental Biology
- Cell Signaling
- Reproductive Biology
Background:
- Ron is a receptor tyrosine kinase activated by hepatocyte growth factor-like (HGFL) protein.
- Mutations in Ron lead to invasive phenotypes, while its deletion causes embryonic lethality.
- The roles of Ron and HGFL in embryo implantation are not fully understood.
Purpose of the Study:
- To investigate the temporal and spatial distribution of Ron during mouse embryo implantation and placentation.
- To determine the functional effects of Ron activation on trophoblast cells.
Main Methods:
- Reverse transcription-polymerase chain reaction (RT-PCR) for transcript localization.
- In situ hybridization and immunohistochemistry for protein distribution.
- Matrigel invasion and cell survival assays on trophoblast cell lines.
Main Results:
- Ron and HGFL transcripts were detected in various reproductive tissues, including the uterus and placenta.
- Ron expression was observed in key embryonic and trophoblast cells during implantation.
- HGFL stimulation increased trophoblast cell invasion and survival in vitro.
Conclusions:
- Ron and HGFL play significant roles in mouse embryo implantation and placentation.
- Ron activation by HGFL supports trophoblast function, enhancing invasion and viability.
- This signaling pathway is critical for successful pregnancy establishment.
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