Background Trans-sutural distraction osteogenesis (TSDO) involves the application of distraction force to facial sutures to stimulate osteogenesis. Gli1 + cells in the cranial sutures play an important role in bone growth. However, whether Gli1 + cells in facial sutures differentiate into bone under distraction force is unknown. Methods 4-week-old Gli1ER/Td and C57BL/6 mice were used to establish a TSDO model to explore osteogenesis of zygomaticomaxillary sutures. A Gli1 + cell lineage tracing model was used to observe the distribution of Gli1 + cells and explore the role of Gli1 + cells in facial bone remodeling. Results Distraction force promoted bone remodeling during TSDO. Fluorescence and two-photon scanning images revealed the distribution of Gli1 + cells. Under distraction force, Gli1-lineage cells proliferated significantly and co-localized with Runx2 + cells. Hedgehog signaling was upregulated in Gli1 + cells. Inhibition of Hedgehog signaling suppresses the proliferation and osteogenesis of Gli1 + cells induced by distraction force. Subsequently, the stem cell characteristics of Gli1 + cells were identified. Cell-stretching experiments verified that mechanical force promoted the osteogenic differentiation of Gli1 + cells through Hh signaling. Furthermore, immunofluorescence staining and RT-qPCR experiments demonstrated that the primary cilia in Gli1 + cells exhibit Hedgehog-independent mechanosensitivity, which was required for the osteogenic differentiation induced by mechanical force. Conclusions Our study indicates that the primary cilia of Gli1 + cells sense mechanical stimuli, mediate Hedgehog signaling activation, and promote the osteogenic differentiation of Gli1 + cells in zygomaticomaxillary sutures.
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Jin et al. (2024) studied this question.
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