Results 1 to 10 of about 66,646 (140)

USP8-mediated mitochondrial regulation in osteoclasts is essential for skeletal development [PDF]

open access: yesCellular and Molecular Life Sciences
Aberrant protein regulatory pathways disrupt bone development and contribute to skeletal diseases. The cysteine protease family of deubiquitinating enzymes (DUBs) are critical for regulation of bone-resorbing osteoclasts and bone-forming osteoblasts ...
Sachin Chaugule   +4 more
doaj   +2 more sources

Osteoclasts and Microgravity [PDF]

open access: yesLife, 2020
Astronauts are at risk of losing 1.0% to 1.5% of their bone mass for every month they spend in space despite their adherence to diets and exercise regimens designed to protect their musculoskeletal systems. This loss is the result of microgravity-related
John Kelly Smith
doaj   +5 more sources

Zoledronic acid promotes osteoclasts ferroptosis by inhibiting FBXO9-mediated p53 ubiquitination and degradation [PDF]

open access: yesPeerJ, 2021
Bisphosphonates (BPs)-related osteonecrosis of jaw (BRONJ) is a severe complication of the long-term administration of BPs. The development of BRONJ is associated with the cell death of osteoclasts, but the underlying mechanism remains unclear.
Xingzhou Qu   +3 more
doaj   +2 more sources

Inhibitory Effects of Gold and Silver Nanoparticles on the Differentiation into Osteoclasts In Vitro

open access: yesPharmaceutics, 2021
Gold nanoparticles (GNPs) have been widely studied to inhibit differentiation into osteoclasts. However, reports of the inhibitory effects of silver nanoparticles (SNPs) during the process of differentiation into osteoclasts are rare.
Daye Lee   +6 more
doaj   +1 more source

A New Method to Sort Differentiating Osteoclasts into Defined Homogeneous Subgroups

open access: yesCells, 2022
Osteoclasts regulate skeletal development but also drive pathological osteolysis, making them prime therapeutic targets. Osteoclast research is limited by the heterogeneity of osteoclast populations generated in vitro, where the mixture of ...
Philippa A. Hulley, Helen J. Knowles
doaj   +1 more source

Arthritis-associated osteoclastogenic macrophages (AtoMs) participate in pathological bone erosion in rheumatoid arthritis

open access: yesImmunological Medicine, 2022
Rheumatoid arthritis is a chronic form of arthritis that causes bone destruction in joints such as the knees and fingers. Over the past two decades, the clinical outcomes of rheumatoid arthritis have improved substantially with the development of ...
Tomoya Agemura   +4 more
doaj   +1 more source

Loss of mutual protection between human osteoclasts and chondrocytes in damaged joints initiates osteoclast-mediated cartilage degradation by MMPs

open access: yesScientific Reports, 2021
Osteoclasts are multinucleated, bone-resorbing cells. However, they also digest cartilage during skeletal maintenance, development and in degradative conditions including osteoarthritis, rheumatoid arthritis and primary bone sarcoma.
Quitterie C. Larrouture   +5 more
doaj   +1 more source

Osteoclast activated FoxP3+ CD8+ T-cells suppress bone resorption in vitro. [PDF]

open access: yesPLoS ONE, 2012
Osteoclasts are the body's sole bone resorbing cells. Cytokines produced by pro-inflammatory effector T-cells (T(EFF)) increase bone resorption by osteoclasts.
Zachary S Buchwald   +4 more
doaj   +1 more source

Origin of Osteoclasts: Osteoclast Precursor Cells

open access: yesJournal of Bone Metabolism, 2023
Osteoclasts are multinucleated bone-resorbing cells and a key player in bone remodeling for health and disease. Since the discovery of osteoclasts in 1873, the structure and function of osteoclasts and the molecular and cellular mechanisms of osteoclastogenesis have been extensively studied.
Jefferson Tsai   +4 more
openaire   +2 more sources

Generation of gene-corrected functional osteoclasts from osteopetrotic induced pluripotent stem cells

open access: yesStem Cell Research & Therapy, 2020
Background Infantile malignant osteopetrosis (IMO) is an autosomal recessive disorder characterized by non-functional osteoclasts and a fatal outcome early in childhood. About 50% of patients have mutations in the TCIRG1 gene.
Xiaojie Xian   +7 more
doaj   +1 more source

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