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Updated: Jun 20, 2026

Isolation and Time-Lapse Imaging of Primary Mouse Embryonic Palatal Mesenchyme Cells to Analyze Collective Movement Attributes
Published on: February 13, 2021
Transforming growth factor-beta3 expression up-regulates on cleft palates induced by
Li-qiang Gan1, Yue-xian Fu, Xing Liu
1Department of Pediatric Surgery, Chongqing Children's Hospital, Chongqing Medical University, Chongqing, China.
Abstract:
2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) has been shown to induce cleft palate, in which the molecular etiology of the defect is poorly characterized. Recently, transforming growth factor-beta3 (TGF-beta3) has been indicated to play an essential role in the development of palatal shelves. In this developmental toxicity study, we investigated the effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on the expression of TGF-beta3 in fetal mice. Pregnant C57BL/6 mice were exposed to corn oil or TCDD (32 microg/kg/day 64 microg/kg/day, per os) at embryonic day 10 (ED10), a drastic inhibition of palatal shelves was induced. By using RT-PCR (reverse transcription-polymerase chain reaction) and Western blot, the expressions of TGF-beta3 was investigated. We found that the expression of TGF-beta3 was gradually up-regulated in TCDD-treated group. These results suggest that cleft palate can be induced by TCDD exposure, the modification of TGF-beta3 is related to its pathogenesis.
Insights
Exposure to 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) can cause cleft palate in fetal mice. This study found TCDD exposure up-regulates transforming growth factor-beta3 (TGF-beta3), suggesting a link to the developmental defect.
Area of Science:
- Developmental toxicology
- Molecular biology
- Teratology
Background:
- 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a known teratogen that can induce cleft palate, but its precise molecular mechanisms remain unclear.
- Transforming growth factor-beta3 (TGF-beta3) is crucial for normal palatal shelf development.
Purpose of the Study:
- To investigate the impact of TCDD exposure on TGF-beta3 expression during palate development.
- To explore the role of TGF-beta3 modulation in TCDD-induced cleft palate pathogenesis.
Main Methods:
- Pregnant C57BL/6 mice were administered TCDD or a control vehicle on embryonic day 10.
- Palatal shelf development was assessed for inhibition.
- Messenger RNA and protein levels of TGF-beta3 were quantified using RT-PCR and Western blot analysis.
Main Results:
- TCDD exposure led to significant inhibition of palatal shelf development.
- Expression of TGF-beta3 was observed to be gradually up-regulated in response to TCDD treatment.
- A correlation between altered TGF-beta3 levels and TCDD-induced cleft palate was identified.
Conclusions:
- TCDD exposure can induce cleft palate in mice.
- The observed up-regulation of TGF-beta3 is implicated in the molecular pathogenesis of TCDD-induced cleft palate.
- Further research into TGF-beta3 signaling pathways may offer insights into preventing or treating TCDD-related developmental defects.
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