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Updated: Aug 17, 2025

Propagation of Dental and Respiratory Cells and Organs in Microgravity
Published on: May 25, 2021
Protection of primary cilia is an effective countermeasure against the impairment of osteoblast function induced by
Jing Liu1, Fei-Fan Leng2, Yu-Hai Gao1
1Fundamental Medical Science Research Laboratories, The 940th Hospital of Joint Logistic Support Force, People's Liberation Army of China, Lanzhou, China.
Abstract:
The molecular mechanism for the microgravity-induced decrease in bone formation remains unclear and there is a lack of effective specific preventative therapies. We recently reported that primary cilia of osteoblasts became shorter and even disappeared when the cells were exposed to random positioning machine (RPM)-simulated microgravity and that the microgravity-induced loss of osteogenic potential of osteoblasts could be attenuated when the resorption of primary cilia was prevented by treatment with 0.1 μM cytochalasin D. In the current study, it was further found that the loss of the osteogenic capacity of rat calvarial osteoblasts (ROBs) was associated with the inhibition of the BMP-2/Smad1/5/8 signalling pathway, of which most of the signalling proteins including BMP-2, BMPRII, Smad1/5/8 and p-Smad1/5/8 were found localized to primary cilia. Accompanying the resorption of primary cilia following the cells being exposed to simulated microgravity, the expression levels of these signalling proteins were reduced significantly. Furthermore, the expression of miRNA-129-3p, a microRNA previously reported to control cilium biogenesis, was found to be reduced quickly and changed in a similar tendency with the length of primary cilia. Moreover, overexpression of miRNA-129-3p in ROBs significantly attenuated microgravity-induced inhibition of BMP-2 signalling and loss of osteogenic differentiation and mineralization. These results indicated the important role of miRNA-129-3p in microgravity-induced resorption of primary cilia of osteoblasts and the potential of replenishing the miRNA-129-3p as an effective countermeasure against microgravity-induced loss of primary cilia and impairment of osteoblast function.
Insights
Microgravity shortens osteoblast primary cilia, impairing bone formation by inhibiting BMP-2 signaling. Restoring miRNA-129-3p levels counteracts this, suggesting a potential therapy for spaceflight-induced bone loss.
Area of Science:
- Cell Biology
- Bone Biology
- Space Biology
Background:
- Microgravity's impact on bone formation is poorly understood, lacking specific preventative therapies.
- Previous research showed microgravity shortens osteoblast primary cilia, reducing osteogenic potential.
- Primary cilia are crucial for osteoblast function and mechanotransduction.
Purpose of the Study:
- To elucidate the molecular mechanism of microgravity-induced bone loss.
- To investigate the role of miRNA-129-3p in primary cilia regulation under microgravity.
- To explore miRNA-129-3p as a potential therapeutic target for microgravity-induced bone loss.
Main Methods:
- Simulated microgravity using a random positioning machine (RPM) on rat calvarial osteoblasts (ROBs).
- Analysis of BMP-2/Smad1/5/8 signaling pathway proteins localization and expression.
- Assessment of miRNA-129-3p expression and its functional role via overexpression.
Main Results:
- Microgravity inhibited BMP-2/Smad1/5/8 signaling, with key proteins localized to primary cilia.
- Primary cilia resorption under microgravity correlated with reduced signaling protein expression.
- Microgravity decreased miRNA-129-3p expression, mimicking primary cilia length changes.
- Overexpression of miRNA-129-3p rescued BMP-2 signaling and osteogenic differentiation.
Conclusions:
- miRNA-129-3p plays a critical role in microgravity-induced primary cilia resorption in osteoblasts.
- Restoring miRNA-129-3p levels can counteract microgravity-induced impairment of osteoblast function.
- miRNA-129-3p replenishment is a promising therapeutic strategy against spaceflight-related bone loss.
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