Bone Cells and Tissue
Bone Structure
Compact Bone
The Bone Matrix
Bone as Supporting Connective Tissue
Spongy Bone
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Updated: Jun 19, 2026

Analysis of Minerals Produced by hFOB 1.19 and Saos-2 Cells Using Transmission Electron Microscopy with Energy Dispersive X-ray Microanalysis
Published on: June 24, 2018
1Department of Pathology, Harvard Medical School, and the Edwin S. Webster Memorial Laboratory of the Department of Pathology, Massachusetts General Hospital, Boston.
This study used electron microscopy to examine the ultrastructure of bone cells in human and chick bone. The researchers described the fine structure of osteoblasts, osteocytes, and osteoclasts in their natural environment. Active osteoblasts were found to have abundant granular endoplasmic reticulum and cytoplasmic processes that extend into the osteoid. The transition from osteoblasts to osteocytes involved a reduction in cytoplasmic organelles. Osteocytes were surrounded by an amorphous layer between the cell and bone cavity walls. Osteoclasts had a distinct structure with numerous ribosomes and mitochondria but little granular endoplasmic reticulum. The brush border of osteoclasts was adjacent to resorption zones, and no unmineralized collagen was observed at these sites. The study also identified endosteal lining cells as a distinct type of bone surface cell. These findings provide a detailed view of bone cell morphology and function.
09:07A Human Bone Marrow 3D Model to Investigate the Dynamics and Interactions Between Resident Cells in Physiological or Tumoral Contexts
Published on: December 16, 2022
09:31Automated Quantification of Hematopoietic Cell – Stromal Cell Interactions in Histological Images of Undecalcified Bone
Published on: April 8, 2015
Area of Science:
Background:
The structure of bone cells remains partially understood, especially at the ultrastructural level. Prior research has shown that bone cells exist in a dynamic environment, but their detailed morphology and interactions are less clear. No prior work had resolved the fine structure of osteoblasts, osteocytes, and osteoclasts in their natural setting. This gap motivated the need for electron microscopic studies of undecalcified bone. The role of cell organelles in bone formation and resorption is not fully established. The presence of amorphous layers near osteocytes and their processes is a newly observed feature. The absence of collagen at resorption sites challenges existing models of bone breakdown. This paper contributes a detailed ultrastructural analysis of bone cell types in human and chick bone.
Purpose Of The Study:
This study aimed to describe the ultrastructural features of bone cells in their native environment. The researchers focused on human woven and chick lamellar bone using electron microscopy. The goal was to trace the morphological changes during osteoblast-to-osteocyte transition. The study also sought to clarify the structure of osteoclasts and their resorption mechanisms. The presence of endosteal lining cells was another key objective. The researchers wanted to visualize the early stages of mineralization and osteoid formation. The study aimed to provide a comprehensive view of bone cell interactions. This work fills a gap in understanding bone cell ultrastructure and function.
Main Methods:
The researchers used Araldite-embedded, undecalcified bone samples from human and chick specimens. Electron microscopy was the primary technique for visualizing cellular structures. The study focused on osteoblasts, osteocytes, and osteoclasts in their natural setting. The transition of osteoblasts into osteocytes was examined through serial sections. The morphology of osteoclasts was compared to other bone cell types. The presence of amorphous material near osteocytes was documented. The resorption zone of osteoclasts was analyzed for collagen and mineral content. The study included detailed illustrations of osteoid and mineralization sites.
Main Results:
Active osteoblasts showed abundant granular endoplasmic reticulum and small vesicles. Their cytoplasmic processes extended into the osteoid matrix. The transition to osteocytes involved a reduction in cytoplasmic organelles. Osteocytes were surrounded by an amorphous layer between the cell and bone cavity walls. Osteoclasts had numerous ribosomes and mitochondria but little granular endoplasmic reticulum. The brush border of osteoclasts was adjacent to resorption zones in bone. No unmineralized collagen was observed at resorption sites. The study revealed that collagen removal occurs before or during mineral dissolution.
Conclusions:
The study traced the morphological changes during osteoblast-to-osteocyte transition. The presence of amorphous material near osteocytes was a novel observation. Osteoclasts differ significantly from other bone cells in their organelle composition. The absence of collagen at resorption sites suggests a specific sequence of events. The brush border of osteoclasts is linked to active resorption. Endosteal lining cells were identified as a distinct cell type. The structure of osteoid and early mineralization was visualized in detail. These findings enhance the understanding of bone cell ultrastructure and function.
The study found that osteoblasts transition into osteocytes with a reduction in cytoplasmic organelles.
Electron microscopy was used on Araldite-embedded, undecalcified bone samples.
The amorphous layer is interposed between the cell and bone cavity walls, suggesting a functional role.
Osteoclasts have numerous ribosomes and mitochondria but little granular endoplasmic reticulum.
No unmineralized collagen was seen, indicating collagen removal before or during mineral dissolution.
Endosteal lining cells cover bone surfaces and lack distinctive features of other bone cell types.