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Related Concept Videos

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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Microarray profile of gene expression during osteoclast differentiation in modelled microgravity.

Yuvaraj Sambandam1, Jeremy J Blanchard, Giffin Daughtridge

  • 1Charles P. Darby Children's Research Institute, Medical University of South Carolina, Charleston, South Carolina 29425, USA.

Journal of Cellular Biochemistry
|August 19, 2010
PubMed
Summary

Microgravity accelerates bone loss by increasing osteoclast activity. This study simulated microgravity and found increased osteoclast differentiation, identifying S100A8 as a key factor in preventing astronaut bone loss.

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Area of Science:

  • Space Biology
  • Cell Biology
  • Bone Physiology

Background:

  • Spaceflight-induced microgravity causes significant bone mass loss in astronauts.
  • Osteoclasts (OCLs) are critical multinucleated cells responsible for bone resorption.

Purpose of the Study:

  • To investigate the molecular mechanisms underlying enhanced osteoclastogenesis under simulated microgravity.
  • To identify potential therapeutic targets for preventing bone loss during space missions.

Main Methods:

  • Simulated microgravity using a rotating wall vessel bioreactor (RWV/RCCS).
  • Gene expression profiling via Agilent microarray analysis of RAW 264.7 OCL progenitor cells.
  • Analysis of calcium levels and siRNA-mediated knockdown of S100A8.

Main Results:

  • Simulated microgravity significantly increased osteoclastogenesis (2-fold) compared to normal gravity.
  • Upregulation of transcription factors (c-Jun, MITF, CREB) and identification of high S100A8 expression.
  • Elevated cytosolic calcium and reduced OCL differentiation upon S100A8 knockdown.

Conclusions:

  • Simulated microgravity enhances osteoclast differentiation and function through specific molecular pathways.
  • S100A8 and calcium signaling are key regulators of osteoclast activity in microgravity.
  • Findings offer insights into therapeutic strategies to mitigate bone loss in astronauts.