98%
921
2 minutes
20
Purpose Of Review: Bone matrix is a multiscale composite material mainly composed of collagen, crystalline apatite mineral, water, and a small amount of non-collagenous proteins. Nested within bone matrix, mechanosensitive osteocytes orchestrate bone adaptation to mechanical loading, which is affected by the ultrastructural composition and mechanical properties of the osteocyte-surrounding bone matrix. In this review, we shed light on the impact of ageing-related modifications in ultrastructural composition of bone matrix on the mechanosensitivity of osteocytes.
Recent Findings: Ageing modulates the ultrastructural composition of bone matrix, such as collagen cross-links, mineral crystal size, microcracks, content of bound water, content and phosphorylation of non-collagenous proteins, and degree of mineralization. These ageing-related modifications alter the mechanical properties of bone matrix, and the biological function of bone, i.e. altered mechanical properties lead to changes in mechanical loading-induced fluid shear stress experienced by osteocytes, which affect osteocyte mechanosensitivity. A better understanding of the role of osteocyte mechanosensitivity in bone adaptation to mechanical loading during ageing is crucial. This review highlights the ageing-related changes in the ultrastructural composition and mechanical properties of bone matrix, that might affect the mechanosensitivity of osteocytes. By linking ageing-related changes in the bone matrix to alterations in osteocyte mechanosensitivity, it is assumed that ageing-modulated bone matrix affects bone adaptation to mechanical loading orchestrated by osteocytes. A comprehensive understanding of how age-related changes in bone matrix composition influence osteocyte mechanosensitivity is crucial for explaining the fragility of ageing bone, as osteocytes are the most abundant and mechanosensitive cells in bone tissue.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12343736 | PMC |
http://dx.doi.org/10.1007/s11914-025-00927-0 | DOI Listing |
Methods Cell Biol
September 2025
Department of Cell Biology and Histology, University of the Basque Country UPV/EHU, Leioa, Spain. Electronic address:
Human Dental Pulp Stem Cells (hDPSCs) represent a remarkable cell source for tissue engineering and regenerative medicine, offering significant potential for use in personalized medicine and autologous therapies. Decellularized extracellular matrix (ECM)-derived biological scaffolds show excellent properties for supporting cell delivery and growth in both in vitro and in vivo applications. These scaffolds provide essential biochemical cues that regulate cellular functions and offer a more accurate representation of the in vivo environment.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Shenzhen College of Advanced Technology, University of Chinese Academy of Sciences, Beijing, 100049, China; Research Center for Cancer Immunology, Institute of Biomedicine and Biotechnology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China. Electronic
Within the bone microenvironment, the intricate interplay and regulation among matrix components form a complex network. Disentangling this network is crucial for uncovering potential therapeutic targets in bone pathology. Osteocalcin (OCN), the most abundant non-collagenous bone protein, is an essential node within this network.
View Article and Find Full Text PDFBiomed Mater
September 2025
School of Chemical, Materials and Biological Engineering, The University of Sheffield, Pam Liversidge Building, Mappin Street, Sheffield, S1 3JD, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
A key challenge in bone tissue engineering (BTE) is designing structurally supportive scaffolds, mimicking the native bone matrix, yet also highly porous to allow nutrient diffusion, cell infiltration, and proliferation. This study investigated the effect of scaffold interconnectivity on human bone marrow stromal cell (BMSC) behaviour. Highly interconnected, porous scaffolds (polyHIPEs) were fabricated using the emulsion templating method from 2-ethylhexyl acrylate/isobornyl acrylate (IBOA) and stabilised with ~200 nm IBOA particles.
View Article and Find Full Text PDFPLoS One
September 2025
Department of Orthopedic Surgery, Center for Shoulder and Elbow Surgery, Konkuk University School of Medicine, Seoul, Korea.
Purpose: We aimed to compare the effects of atelocollagen (AC) and individual growth factors on the expression of key molecular markers associated with tendon healing.
Methods: C2C12 myoblasts were cultured in Dulbecco's Modified Eagle Medium (DMEM) containing 5% fetal bovine serum (FBS) and treated with 1 nM or 10 nM of Atelocollagen (AC), bone morphogenetic protein-2 (BMP-2), transforming growth factor-beta 1 (TGF-β1), insulin-like growth factor-1 (IGF-1), or vascular endothelial growth factor (VEGF) for 5 days. After 5 days of treatment, cells were harvested from the culture medium, and Western blot analysis was performed to quantify the expression of phosphorylated extracellular signal-regulated kinase (p-ERK), Collagen type I (Col I), Collagen type Ⅲ (Col Ⅲ), and Tenascin C (TnC).
Adv Pharm Bull
July 2025
Department of Hematology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Purpose: The survival and progression of multiple myeloma (MM) cells rely heavily on supportive factors and cells within the MM microenvironment, notably macrophages. The PI3K signaling pathway plays a crucial role in both myeloma cells survival and macrophage polarity, making it a potential target for altering the MM microenvironment dynamics.
Methods: In this study, the impact of LY294002, a PI3K signaling pathway inhibitor, on the viability of U266 myeloma cells in mono-culture and MM patient-derived bone marrow mononuclear cells (BM-MNCs) in co-culture was investigated.