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Updated: Oct 14, 2025

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Isolation and Time-Lapse Imaging of Primary Mouse Embryonic Palatal Mesenchyme Cells to Analyze Collective Movement Attributes
Published on: February 13, 2021
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Spatiotemporal Expression and Functional Analysis of miRNA-22 in the Developing Secondary Palate
Partha Mukhopadhyay1, Irina Smolenkova1, Ratnam S Seelan1
1Department of Oral Immunology and Infectious Diseases, Division of Craniofacial Development and Anomalies, School of Dentistry, 5170University of Louisville, Louisville, KY 40202.
Summary
MicroRNA-22 (miR-22) is crucial for embryonic orofacial development, specifically in removing the midline epithelial seam during palate formation. Dysregulation of miR-22 may contribute to cleft palate.
Area of Science:
- Developmental Biology
- Molecular Biology
- Genetics
Background:
- Embryonic orofacial development requires precise gene coordination.
- MicroRNAs are non-coding RNA molecules regulating gene expression.
- The role of microRNA-22 (miR-22) in murine orofacial development is not fully understood.
Purpose of the Study:
- To investigate the spatiotemporal expression of miR-22 in the developing murine secondary palate.
- To identify potential mRNA targets of miR-22 and their functions.
- To determine the role of miR-22 in secondary palate development and midline epithelial seam removal.
Main Methods:
- In situ hybridization and quantitative real-time PCR for miR-22 expression analysis.
- Bioinformatic analysis to predict miR-22 mRNA targets.
- In vitro palate organ culture to assess miR-22 function.
Main Results:
- miR-22 expression increased progressively in palatal processes from embryonic day (GD) 12.5 to GD14.5.
- miR-22 was detected in specific epithelial and mesenchymal tissues during palate development.
- Inhibition of miR-22 disrupted midline epithelial seam removal, indicating its critical role.
Conclusions:
- miR-22 plays a key role in midline epithelial seam removal during palatogenesis.
- miR-22 may be a significant factor in the etiology of cleft palate.

