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Related Concept Videos

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.
Bone Remodeling and Repair01:31

Bone Remodeling and Repair

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...
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...
Bone Structure01:55

Bone Structure

Within the skeletal system, the structure of a bone, or osseous tissue, can be exemplified in a long bone, like the femur, where there are two types of osseous tissue: cortical and cancellous.
The Bone Matrix01:18

The Bone Matrix

Bone contains a relatively small number of cells entrenched in a matrix of collagen fibers that provide an adherent surface for inorganic salt crystals. Both components of the matrix, organic and inorganic, contribute to the unusual properties of bone. Without collagen, bones would be brittle and shatter easily. Without mineral crystals, bones would flex and provide little support. This can be observed by an experiment: when the minerals of a bone are dissolved by soaking the bone in acid or...
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...

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Using Inducible Osteoblastic Lineage-Specific Stat3 Knockout Mice to Study Alveolar Bone Remodeling During Orthodontic Tooth Movement
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Model structure and control of bone remodeling: a theoretical study.

Peter Pivonka1, Jan Zimak1, David W Smith1

  • 1Department of Civil and Environmental Engineering, University of Melbourne, VIC 3010, Australia.

Bone
|June 3, 2008
PubMed
Summary

This study models bone remodeling, revealing a preferred RANKL/OPG expression profile that aligns with biological observations and suggests optimal TGF-beta signaling for bone volume regulation.

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Area of Science:

  • Bone Biology and Remodeling
  • Computational Biology
  • Cell Signaling

Background:

  • The RANK-RANKL-OPG signaling pathway is crucial for bone remodeling.
  • The specific expression profiles of RANKL and OPG in osteoblast precursors and mature osteoblasts, respectively, and their functional role in the basic multicellular unit (BMU) remain incompletely understood.

Purpose of the Study:

  • To theoretically investigate the functional implications of specific RANKL/OPG expression profiles on bone volume.
  • To model the interplay between RANK-RANKL-OPG signaling, TGF-beta, and bone cell dynamics within the BMU.

Main Methods:

  • Formulation of an extended bone-cell dynamics model incorporating RANK-RANKL-OPG and TGF-beta signaling.
  • Inclusion of rate equations for bone volume changes and TGF-beta release.
  • Modification of cell line expression profiles and activator/repressor functions.

Main Results:

  • A preferred arrangement of ligand expression on specific cell types was identified, correlating with existing biological observations.
  • Combinatorial analysis of parameter changes identified potentially significant groupings for controlling BMU responses.
  • Parameter changes related to TGF-beta signaling yielded a unique result with a clear biological rationale.

Conclusions:

  • The study provides a theoretical framework explaining the functional significance of RANKL/OPG expression profiles in bone remodeling.
  • The findings suggest optimal control strategies for BMU activity through modulation of cell differentiation rates.
  • The research offers a theoretical explanation for the biological effects of TGF-beta on bone cell differentiation.