Specific mitotic events drive left-right organizer development

Cell proliferation is crucial for tissue development. Here, we investigate its role in the left-right organizer, which establishes the left-right axis. In zebrafish, we mapped mitotic events in Kupffer's vesicle (KV) and identified an anteriorly enriched, FGF-dependent mitotic pattern. Laser ablation of mitotic cells and pericentrin-null mutants, both reducing mitotic events, resulted in smaller lumens, confirming that cell division is essential for KV development. Pericentrin-null mutants also exhibited defects in leftward cardiac jogging, indicative of KV dysfunction. Using a KV-specific fluorescent microtubule marker, we found that the KV rosette is a transient, centrally organized cluster interconnected by cytokinetic bridges and containing microtubule bundles. This structure emerges after the first four divisions and precedes lumen formation. Mitotic events during KV rounding coincide with rosette formation, spindle rotation and cell extrusion, likely driven by increased packing. Eliminating the first four mitotic events disrupted rosette formation and prevented normal KV rounding. These findings demonstrate that mitotic events are crucial for KV development, with cell division timing shaping KV architecture and function.

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Publication Details

Journal
Development
Published
2025-04-15
DOI
https://doi.org/10.1242/dev.204687
Citations
4
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
3.22

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Specific mitotic events drive left-right organizer development

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4 citations
Development
Congenital heart defects research
3.22
article

Specific mitotic events drive left-right organizer development

Favour Ononiwu, Heidi Hehnly, Kirsten Rasmussen, Li-En Jao, Jonah Da Silva, Yiling Lan, Abdalla Wael Shamil, Yan Wu, A. Robin Poole
article en
4 citations

Abstract

Cell proliferation is crucial for tissue development. Here, we investigate its role in the left-right organizer, which establishes the left-right axis. In zebrafish, we mapped mitotic events in Kupffer's vesicle (KV) and identified an anteriorly enriched, FGF-dependent mitotic pattern. Laser ablation of mitotic cells and pericentrin-null mutants, both reducing mitotic events, resulted in smaller lumens, confirming that cell division is essential for KV development. Pericentrin-null mutants also exhibited defects in leftward cardiac jogging, indicative of KV dysfunction. Using a KV-specific fluorescent microtubule marker, we found that the KV rosette is a transient, centrally organized cluster interconnected by cytokinetic bridges and containing microtubule bundles. This structure emerges after the first four divisions and precedes lumen formation. Mitotic events during KV rounding coincide with rosette formation, spindle rotation and cell extrusion, likely driven by increased packing. Eliminating the first four mitotic events disrupted rosette formation and prevented normal KV rounding. These findings demonstrate that mitotic events are crucial for KV development, with cell division timing shaping KV architecture and function.

DevelopmentVol. 152(10)
Worcester Polytechnic Institute (US), Syracuse University (US), University of California, Davis (US)
Syracuse University, State University of New York, State University of New York Upstate Medical University, National Institute of General Medical Sciences
Openalex Percentile: Top 9%
Congenital heart defects research
3.22
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