# Early increased cell proliferation compensates subsequent hypoplasia of the ossicle

**Authors:** Katsushige Kawasaki, Maiko Kawasaki, Finsa Tisna Sari, Vanessa Utama, Alex Kesuma, Makoto Fukushima, Naoaki Saito, Daisuke Suda, Takehisa Kudo, Akira Fujita, Jun Nihara, Brunella Franco, Atsushi Ohazama

PMC · DOI: 10.3389/fcell.2025.1627730 · Frontiers in Cell and Developmental Biology · 2025-10-29

## TL;DR

Early cell growth can make up for later bone structure issues in mice, offering hope for treating hearing loss caused by ossicle hypoplasia.

## Contribution

Early increased cell proliferation compensates for later ossicle hypoplasia, revealing a novel developmental mechanism.

## Key findings

- Ossicular hypoplasia was partially rescued by early Hh signaling activation.
- Early cell proliferation at E10.5 compensates for later developmental defects.
- SAG application at E9.5 rescued ossicle hypoplasia in mutant mice.

## Abstract

Ossicles are essential structures for normal sound conduction from the external environment to the inner ear. Proper formation of the ossicles is required for normal hearing, and ossicular deformities lead to hearing loss. We identified ossicular hypoplasia in mice with mesenchymal conditional deletion of the primary cilia molecule (Ofd1

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;Wnt1Cre and Ift88

 fl/fl

;Wnt1Cre). Hh signaling activity and cell proliferation were significantly downregulated in ossicle primordia of Ofd1

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;Wnt1Cre mice from E11.5. To restore Hh signaling in Ofd1

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;Wnt1Cre mice, we crossed R26SmoM2

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 mice (a constitutively active form of Smo) with Ofd1

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;Wnt1Cre mice. Ossicular hypoplasia was partially rescued in Ofd1

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;Wnt1Cre;R26SmoM2

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 mice. However, Hh signaling activity was not restored after E11.5. Instead, Hh signaling activity and cell proliferation were significantly increased in Ofd1

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;Wnt1Cre;R26SmoM2

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 mice at E10.5, when these were not altered in Ofd1

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;Wnt1Cre mice. To confirm whether molecular changes at E10.5 rescue subsequent hypoplasia, SAG (agonist of Hh signaling) was applied to Ofd1

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;Wnt1Cre mice at E9.5. A similar rescue could be observed in Ofd1

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;Wnt1Cre mice with SAG application. Thus, early increased cell proliferation could compensate subsequent hypoplasia of ossicle formation. Our results may provide clues for possible future treatment in familial hearing loss due to hypoplasia of the ossicles.

## Linked entities

- **Genes:** OFD1 (OFD1 centriole and centriolar satellite protein) [NCBI Gene 8481], H2az2 (H2A.Z histone variant 2) [NCBI Gene 77605], IFT88 (intraflagellar transport 88) [NCBI Gene 8100]
- **Chemicals:** SAG (PubChem CID 5284330)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Smo (smoothened, frizzled class receptor) [NCBI Gene 319757] {aka E130215L21Rik, Smoh, bnb, smoothened}, Wnt1 (wingless-type MMTV integration site family, member 1) [NCBI Gene 22408] {aka Int-1, Wnt-1, sw, swaying}, Ift88 (intraflagellar transport 88) [NCBI Gene 21821] {aka Tg737, Tg737Rpw, TgN737Rpw, Ttc10, flexo, fxo}, Ofd1 (OFD1, centriole and centriolar satellite protein) [NCBI Gene 237222] {aka Cxorf5, DXGgc7e, ORF2}
- **Diseases:** hearing loss (MESH:D034381), Ossicular hypoplasia (MESH:C537142), hypoplasia (MESH:D000080344), hypoplasia of ossicle formation (MESH:D058426)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12605138/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12605138/full.md

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Source: https://tomesphere.com/paper/PMC12605138