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Published on: May 26, 2011
Regulation of early Xenopus development by ErbB signaling
1Department of Cell Biology, The University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
Abstract:
ErbB signaling has long been implicated in cancer formation and progression and is shown to regulate cell division, migration, and death during tumorigenesis. The functions of the ErbB pathway during early vertebrate embryogenesis, however, are not well understood. Here we report characterization of ErbB activities during early frog development. Gain-of-function analyses show that EGFR, ErbB2, and ErbB4 induce ectopic tumor-like cell mass that contains increased numbers of mitotic cells. Both the muscle and the neural markers are expressed in these ectopic protrusions. ErbBs also induce mesodermal markers in ectodermal explants. Loss-of-function studies using carboxyl terminal-truncated dominant-negative ErbB receptors demonstrate that blocking ErbB signals leads to defective gastrulation movements and malformation of the embryonic axis with a reduction in the head structures in early frog embryos. These data, together with the observation that ErbBs are expressed early during frog embryogenesis, suggest that ErbBs regulate cell proliferation, movements, and embryonic patterning during early Xenopus development.
Insights
Epidermal Growth Factor Receptor (EGFR) signaling pathways regulate cell proliferation and embryonic development. In frogs, ErbB signaling is crucial for cell division, embryonic axis formation, and cell movement during early development.
Area of Science:
- Developmental Biology
- Cell Signaling
- Cancer Biology
Background:
- ErbB signaling is vital in cancer, regulating cell division, migration, and death.
- Its role in early vertebrate embryogenesis remains largely unexplored.
Purpose of the Study:
- To investigate the functions of ErbB signaling during early frog (Xenopus) development.
- To characterize ErbB activities in cell proliferation, movement, and embryonic patterning.
Main Methods:
- Gain-of-function analyses using EGFR, ErbB2, and ErbB4.
- Loss-of-function studies with dominant-negative ErbB receptors.
- Analysis of cell proliferation, marker expression, and embryonic morphology.
Main Results:
- EGFR, ErbB2, and ErbB4 activation induced tumor-like cell masses with increased mitotic activity and expression of muscle, neural, and mesodermal markers.
- Blocking ErbB signaling disrupted gastrulation, malformed the embryonic axis, and reduced head structure development.
Conclusions:
- ErbB signaling is essential for regulating cell proliferation, cell movements, and embryonic patterning in early Xenopus development.
- These findings highlight the conserved role of ErbB pathways in both tumorigenesis and embryonic development.
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