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Related Concept Videos

Bone Disorders01:29

Bone Disorders

Aging and its effect on bone remodeling is the most common cause of bone disorders. In young and healthy people, bone deposition and resorption happen at an equal rate to maintain optimal bone health.
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...
Bone Remodeling01:40

Bone Remodeling

Bone remodeling is a continuous and balanced process of bone resorption by osteoclasts and bone formation by osteoblasts. In adults, it helps maintain bone mass and calcium homeostasis. While mechanical stress can stimulate turnover as part of the normal maintenance and reparative process, several hormones also regulate bone remodeling.
Menopause01:28

Menopause

Menopause, a natural biological process marking the end of a woman's fertility, typically occurs between the fifth and sixth decade of life. This phase is characterized by the exhaustion of the ovarian follicle pool, leading to less responsive ovaries despite the high levels of Follicle Stimulating Hormone (FSH) and Luteinizing Hormone (LH). The consequential decrease in estrogen production results in symptoms like hot flashes, heavy sweating, headaches, hair loss, muscle pains, vaginal...
Osteoclasts in Bone Remodeling01:31

Osteoclasts in Bone Remodeling

Osteoclasts are cells responsible for bone resorption and remodeling. They originate from hematopoietic progenitor cells present in the bone marrow. Numerous progenitor cells fuse to form multinucleated cells, each with 10-20 nuclei. A single osteoclast has a diameter of 150 to 200 µM. These cells have ruffled borders that break down the underlying bone tissue and release minerals such as calcium into the blood in bone resorption. Osteoclasts cling to bones with their ruffled edges during bone...

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Related Experiment Video

Updated: Jun 19, 2026

Studies on the Anti-Inflammatory Effect of Xiaoyao Pills in The Treatment of Postmenopausal Osteoporosis in Mice
07:20

Studies on the Anti-Inflammatory Effect of Xiaoyao Pills in The Treatment of Postmenopausal Osteoporosis in Mice

Published on: August 23, 2024

Immune changes in post-menopausal osteoporosis: the Immunos study.

V Breuil1, M Ticchioni, J Testa

  • 1Service de Rhumatologie, CHU de Nice, Hôpital l'Archet, Nice, France. breuil@unice.fr

Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA
|October 31, 2009
PubMed
Summary

Postmenopausal osteoporosis is linked to immune system changes, including altered B lymphocyte populations and lower interferon-gamma (IFN-gamma) secretion by CD4+ cells, impacting bone health.

Related Experiment Videos

Last Updated: Jun 19, 2026

Studies on the Anti-Inflammatory Effect of Xiaoyao Pills in The Treatment of Postmenopausal Osteoporosis in Mice
07:20

Studies on the Anti-Inflammatory Effect of Xiaoyao Pills in The Treatment of Postmenopausal Osteoporosis in Mice

Published on: August 23, 2024

Area of Science:

  • Immunology
  • Osteoporosis Research
  • Bone-Immune System Interaction

Background:

  • Investigating the interplay between the skeletal and immune systems is crucial for understanding osteoporosis.
  • Previous research has not fully elucidated the immune cell profiles in postmenopausal women with osteoporotic fractures.

Purpose of the Study:

  • To compare the phenotypic and functional characteristics of immune cells in postmenopausal women with osteoporotic fractures versus healthy controls.
  • To identify specific immune cell populations and cytokine profiles associated with osteoporosis.

Main Methods:

  • Analysis of surface markers on peripheral B, CD4+, and CD8+ lymphocytes.
  • Assessment of cytokine secretion (IFN-gamma, GM-CSF) from cultured immune cells.
  • Measurement of bone mineral density (BMD) and body composition using dual-energy X-ray absorptiometry.

Main Results:

  • Osteoporotic women exhibited lower levels of specific B lymphocyte subsets and CD4+ T cells correlated with BMD.
  • Basal secretion of interferon-gamma (IFN-gamma) by CD4+ cells was significantly lower in osteoporotic women.
  • B lymphocytes from osteoporotic women showed increased granulocyte-macrophage colony-stimulating factor (GM-CSF) secretion, correlated with fracture rate.

Conclusions:

  • Postmenopausal osteoporosis is associated with distinct immune system alterations, irrespective of age and estrogen levels.
  • Changes in B lymphocyte populations and IFN-gamma secretion may play a role in osteoporosis pathophysiology.
  • These immune dysregulations could contribute to the frailty and increased morbidity/mortality observed in patients with osteoporotic fractures.