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Updated: Oct 30, 2025

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Published on: May 2, 2025
Effects of advanced glycation end products on osteocytes mechanosensitivity
Xiao Yang1, Cong-Jin Liu1, Zhen-Zhen Wang1
1Key Laboratory for Biomechanics and Mechanobiology of Ministry of Education, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing, China, 100083.
Abstract:
Osteocytes are extremely sensitive to mechanical loading and govern bone remodeling process. Advanced glycation end products (AGEs) have the capacity to induce osteocyte apoptosis. In order to investigate the effects of AGEs on the mechanosensitivity of osteocytes, the osteocytic-like cells (MLO-Y4) were treated with low (50 μg/ml) and high (400 μg/ml) concentrations of AGEs for 1day and exposed to 15 dyne/cm2 of fluid shear stress. Then the F-actin cytoskeleton, prostaglandin E2(PGE2), Nitric oxide (NO), the Wnt/β-catenin signaling pathway activity mRNA expressions were detected for osteocytes mechanical response changes; osteocalcin (OCN) and receptor activator of nuclear factor-kappa B ligand (RANKL)/osteoprotegerin (OPG) were detected for the regulation on bone remodeling function of osteocytes. The results showed that AGEs accumulation inhibited the sense of osteocytes to external mechincal loading, promoted shear-induced NO and PGE2 release, suppressed the mechanosensitivity of Wnt/β-catenin signaling pathway, and furthermore promoted OCN and RANKL/OPG mRNA expressions. These indicated AGEs had an adverse impact on the mechanosensitivity of osteocytes, and led to a negative effect on their regulation of bone remodeling process under mechanical stimulation. This work provides a new perspective to interpret the alteration mechanism of osteocytes mechanosensitivity and provides a novel clue for exploring the mechanism of osteoporosis.
Insights
Advanced glycation end products (AGEs) impair osteocyte mechanosensitivity, disrupting bone remodeling. This study reveals AGEs negatively impact how osteocytes respond to mechanical stress, offering insights into osteoporosis mechanisms.
Area of Science:
- Bone Biology
- Cellular Mechanotransduction
Background:
- Osteocytes are crucial mechanosensors regulating bone remodeling.
- Advanced glycation end products (AGEs) can induce osteocyte apoptosis.
- The impact of AGEs on osteocyte mechanosensitivity remains unclear.
Purpose of the Study:
- To investigate the effects of AGEs on osteocyte mechanosensitivity.
- To determine how AGEs influence osteocyte response to mechanical loading.
- To elucidate AGEs' role in regulating bone remodeling markers.
Main Methods:
- Osteocytic-like cells (MLO-Y4) were treated with varying AGE concentrations.
- Cells were subjected to fluid shear stress (15 dyne/cm²).
- Key mechanotransduction markers (F-actin, PGE2, NO, Wnt/β-catenin) and bone remodeling markers (OCN, RANKL/OPG) were analyzed.
Main Results:
- AGEs inhibited osteocyte response to mechanical loading.
- AGEs enhanced shear-induced Nitric Oxide (NO) and Prostaglandin E2 (PGE2) release.
- AGEs suppressed Wnt/β-catenin pathway mechanosensitivity and promoted OCN and RANKL/OPG mRNA expression.
Conclusions:
- AGEs adversely affect osteocyte mechanosensitivity and bone remodeling regulation.
- AGE accumulation leads to negative effects on osteocytes under mechanical stimulation.
- This study provides novel insights into osteoporosis mechanisms related to osteocyte dysfunction.
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