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The Potential Role of Bone Morphogenetic Protein-2/-4 in Excessive Mechanical Overloading-Initiated Joint
Rong-Ze Hsieh1,2, Kuo-Chin Huang3,4, Yu-Ping Su5,6
1Department of Medical Research and Development, Chiayi Chang Gung Memorial Hospital, Chiayi, Taiwan.
Abstract:
Excessive mechanical overloading of articular cartilage caused by excessive exercise or severe trauma is considered a critical trigger in the development of osteoarthritis (OA). However, the available clinical theranostic molecular targets and underlying mechanisms still require more elucidation. Here, we aimed to examine the possibility that bone morphogenetic proteins (BMPs) serve as molecular targets in rat cartilages and human chondrocytes under conditions of excessive mechanical overloading. Two rat models involving high-intensity running training and surgery for destabilization of medial meniscus, along with a cell model subjected to cyclic tensile strain, were established to simulate and investigate excessive mechanical overloading effects on cartilages/chondrocytes. We employed various methods, including immunohistochemistry, real-time polymerase chain reaction, western blot analysis, and enzyme-linked immunosorbent assay, to evaluate the expression, secretion, phosphorylation, and nuclear translocation of mRNA/proteins in cartilages and chondrocytes. Our findings revealed a simultaneous upregulation of BMP-2 and downregulation of BMP-4 in degenerated and inflamed cartilages and chondrocytes under excessive mechanical overloading. Furthermore, toll-like receptor 2 and nuclear factor kappa B-p50/p65 subunits signaling were identified as regulators governing this distinct expression pattern. Treatment with recombinant BMP-2 and/or BMP-4 proteins significantly ameliorated cartilage degeneration and chondrocyte inflammation induced by excessive mechanical overloading. These results strongly suggest that BMP-2 upregulation and BMP-4 downregulation might represent mechanisms for self-rescue and degeneration in damaged cartilage/chondrocytes, respectively. Our findings advance new insights that BMP-2/-4 might be potential molecular targets for excessive mechanical overloading-caused OA development and should be taken into account in future clinical applications.
Insights
Excessive mechanical stress on cartilage triggers osteoarthritis (OA). Bone morphogenetic proteins (BMPs) like BMP-2 and BMP-4 show altered expression, suggesting they are key targets for OA treatment.
Area of Science:
- Biochemistry
- Cell Biology
- Orthopedics
Background:
- Osteoarthritis (OA) is often initiated by excessive mechanical stress on articular cartilage from intense exercise or trauma.
- Current understanding of molecular targets and mechanisms in OA pathogenesis remains incomplete.
- Bone morphogenetic proteins (BMPs) are investigated for their role in cartilage health and disease.
Purpose of the Study:
- To investigate bone morphogenetic proteins (BMPs) as molecular targets in rat cartilage and human chondrocytes under excessive mechanical overloading.
- To elucidate the mechanisms underlying BMP expression changes in response to mechanical stress.
- To evaluate the therapeutic potential of BMP-2 and BMP-4 in mitigating OA-related cartilage damage.
Main Methods:
- Established rat models (high-intensity running, surgical destabilization of medial meniscus) and a cell model (cyclic tensile strain) to simulate mechanical overloading.
- Utilized immunohistochemistry, real-time PCR, western blot, and ELISA to assess BMP expression, secretion, phosphorylation, and nuclear translocation.
- Investigated the roles of toll-like receptor 2 and NF-κB signaling pathways.
Main Results:
- Observed simultaneous upregulation of BMP-2 and downregulation of BMP-4 in degenerated and inflamed cartilage and chondrocytes under mechanical overload.
- Identified toll-like receptor 2 and NF-κB signaling as regulators of this BMP expression pattern.
- Demonstrated that recombinant BMP-2 and/or BMP-4 treatment significantly reduced cartilage degeneration and chondrocyte inflammation.
Conclusions:
- BMP-2 upregulation and BMP-4 downregulation represent potential self-rescue and degenerative mechanisms in mechanically overloaded cartilage, respectively.
- BMP-2/-4 signaling pathways are implicated in the development of osteoarthritis caused by excessive mechanical loading.
- BMP-2 and BMP-4 are promising molecular targets for future clinical applications in OA prevention and treatment.
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