Long non-coding TRPM2-AS regulates fracture healing by targeting miR-545-3p/Bmp2
- Renjie Kang 1, Lina Huang 2, Teng Zeng 3, Jinliang Ma 4, Danjie Jin 5
- Renjie Kang 1, Lina Huang 2, Teng Zeng 3
- 1Department of Orthopedics, Peking University First Hospital Taiyuan Hospital, Taiyuan, 030000, China.
- 2Department of Rehabilitation Medicine, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, 533000, China.
- 3Department of Orthopedics, The First People's Hospital of Jingzhou, First Affiliated Hospital of Yangtze University, No. 8, Hangkong Road, Shashi District, Jingzhou, 434000, China.
- 4Department of Orthopedics, The First People's Hospital of Jingzhou, First Affiliated Hospital of Yangtze University, No. 8, Hangkong Road, Shashi District, Jingzhou, 434000, China. jindanjie2018@163.com.
- 5Department of Orthopedics, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, No. 68, Gehu Middle Road, Wujin District, Changzhou, 213000, China. majingliang197801@163.com.
- 0Department of Orthopedics, Peking University First Hospital Taiyuan Hospital, Taiyuan, 030000, China.
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View abstract on PubMed
Summary
This summary is machine-generated.Long non-coding RNA (lncRNA) TRPM2-AS is downregulated in delayed fracture healing, impacting osteoblast function. Restoring TRPM2-AS may improve fracture healing by modulating the miR-545-3p/Bmp2 pathway.
Area Of Science
- Molecular Biology
- Orthopedics
- Biochemistry
Background
- Delayed fracture healing poses significant challenges to patient recovery and well-being.
- Understanding the molecular mechanisms underlying delayed fracture healing is crucial for developing effective therapeutic strategies.
Purpose Of The Study
- To investigate the role of long non-coding RNA (lncRNA) TRPM2-AS in delayed fracture healing.
- To elucidate the molecular pathway involving TRPM2-AS, microRNA-545-3p (miR-545-3p), and bone morphogenetic protein 2 (Bmp2) in osteoblast differentiation and fracture healing.
Main Methods
- Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was used to measure the expression of TRPM2-AS, miR-545-3p, Bmp2 mRNA, and osteogenic markers in patients and cells.
- Dual luciferase reporter gene assays were performed to confirm the interaction between TRPM2-AS, miR-545-3p, and Bmp2.
- Cell proliferation and apoptosis were assessed using CCK-8 assays and flow cytometry.
Main Results
- TRPM2-AS was significantly downregulated in delayed fracture healing patients and negatively correlated with fracture healing status.
- TRPM2-AS downregulation suppressed osteogenic marker expression, proliferation, and promoted apoptosis in MC3T3-E1 cells.
- TRPM2-AS inhibited miR-545-3p, which targets Bmp2, thereby impacting osteoblast differentiation.
Conclusions
- TRPM2-AS serves as a potential diagnostic biomarker for delayed fracture healing.
- The TRPM2-AS/miR-545-3p/Bmp2 axis plays a critical role in regulating osteoblast function and fracture healing.
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