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Apical constriction and epithelial invagination are regulated by BMP activity
Vijay K Jidigam1, Raghuraman C Srinivasan1, Cedric Patthey1
1Umeå Centre for Molecular Medicine, Umeå University, Umeå S-901 87, Sweden.
Bone morphogenetic protein (BMP) signals are crucial for epithelial invagination, driving apical constriction and cell elongation by regulating RhoA and F-actin. This study clarifies BMP
Area of Science:
- Developmental Biology
- Cell Biology
- Molecular Biology
Background:
- Epithelial invagination is a key developmental process involving tissue bending and apical constriction.
- While intracellular mechanisms are known, extracellular signals regulating invagination remain understudied.
Purpose of the Study:
- To investigate the role of the extracellular signal Bone Morphogenetic Protein (BMP) in epithelial invagination.
- To determine if BMP regulates processes like apical constriction and cell elongation during placodal invagination.
Main Methods:
- Established in vivo assays for placodal invagination.
- Inhibited BMP activity in prospective cranial placodes.
- Analyzed RhoA and F-actin rearrangements, apical constriction, cell elongation, cell death, and proliferation.
Main Results:
- BMP signaling is essential for RhoA and F-actin rearrangements, apical constriction, cell elongation, and epithelial invagination.
- BMP inhibition disrupts apical accumulation of RhoA and F-actin, leading to failed invagination.
- Epithelial invagination and placode-specific identity acquisition are distinct developmental processes.
Conclusions:
- BMP signals act upstream of intracellular machinery to promote epithelial invagination.
- BMP is required for apical constriction and cell elongation during this process.
- This study elucidates the extracellular regulation of epithelial morphogenesis.
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