Interplay between Inflammation and Pathological Bone Resorption: Insights into Recent Mechanisms and Pathways in Related Diseases for Future Perspectives.

Int J Mol Sci

Department of Orthopedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Kita-15, Nish-7, Kita-ku, Sapporo 060-8638, Japan.

Published: February 2022

AI Article Synopsis

  • Bone is a flexible connective tissue essential for support, protection of organs, and mineral storage, undergoing constant remodeling to maintain its function.
  • Recent research highlights the immune system's role in this remodeling process, with chronic inflammation being a key factor that can lead to excessive bone loss.
  • Osteolytic diseases, caused by this imbalance, represent a major public health issue, prompting investigation into cellular mechanisms and treatment strategies for managing these conditions.

Article Abstract

Bone is a mineralized and elastic connective tissue that provides fundamental functions in the human body, including mechanical support to the muscles and joints, protection of vital organs and storage of minerals. Bone is a metabolically active organ that undergoes continuous remodeling processes to maintain its architecture, shape, and function throughout life. One of the most important medical discoveries of recent decades has been that the immune system is involved in bone remodeling. Indeed, chronic inflammation has been recognized as the most significant factor influencing bone homeostasis, causing a shift in the bone remodeling process toward pathological bone resorption. Bone osteolytic diseases typified by excessive bone resorption account for one of the greatest causes of disability worldwide, with significant economic and public health burdens. From this perspective, we discuss the recent findings and discoveries highlighting the cellular and molecular mechanisms that regulate this process in the bone microenvironment, in addition to the current therapeutic strategies for the treatment of osteolytic bone diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836472PMC
http://dx.doi.org/10.3390/ijms23031786DOI Listing

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