Ossification

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Ossification (also called osteogenesis or bone mineralization) in bone remodeling is the process of laying down new bone material by cells named osteoblasts. It is synonymous with bone tissue formation.[1] There are two processes resulting in the formation of normal, healthy bone tissue:[2] Intramembranous ossification is the direct laying down of bone into the primitive connective tissue (mesenchyme), while endochondral ossification involves cartilage as a precursor.

Bone is broken down by osteoclasts, and rebuilt by osteoblasts, both of which communicate through cytokine (TGF-β, IGF) signalling.

In fracture healing, endochondral osteogenesis is the most commonly occurring process, for example in fractures of long bones treated by plaster of Paris, whereas fractures treated by open reduction and internal fixation with metal plates, screws, pins, rods and nails may heal by intramembranous osteogenesis.

Heterotopic ossification is a process resulting in the formation of bone tissue that is often atypical, at an extraskeletal location. Calcification is often confused with ossification. Calcification is synonymous with the formation of calcium-based salts and crystals within cells and tissue. It is a process that occurs during ossification, but not necessarily vice versa.

The exact mechanisms by which bone development is triggered remains unclear, but growth factors and cytokines appear to play a role.

Time period[3] Bones affected[3]
Third month of fetal development Ossification in long bones beginning
Fourth month Most primary ossification centers have appeared in the diaphyses of bone.
Birth to five years Secondary ossification centers appear in the epiphyses
five years to 12 years in females, 5 to 14 years in males Ossification is spreading rapidly from the ossification centers and various bones are becoming ossified.
17 to 20 years Bone of upper limbs and scapulae becoming completely ossified
18 to 23 years Bone of the lower limbs and os coxae become completely ossified
23 to 26 years Bone of the sternum, clavicles, and vertebrae become completely ossified
By 25 years Nearly all bones are completely ossified

Intramembranous ossification

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Intramembranous ossification forms the flat bones of the skull, mandible and hip bone.

Osteoblasts cluster together to create an ossification center. They then start secreting osteoid, an unmineralized collagen-proteoglycan matrix that has the ability to bind calcium. As calcium binds to the osteoid, the matrix hardens, and the osteoblasts become entrapped, transforming into osteocytes.

As osteoblasts continue to secrete osteoid, it surrounds blood vessels, leading to the formation of trabecular (cancellous or spongy) bone. These blood vessels will eventually develop into red bone marrow. Mesenchymal cells on the bone surface form a membrane known as the periosteum. Osteoblasts secrete osteoid in parallel with the existing matrix, creating layers of compact (cortical) bone.[4]

Endochondral ossification

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Diagram showing stages of endochondral ossification

Endochondral ossification is the formation of long bones and other bones. This requires a hyaline cartilage precursor. There are two centers of ossification for endochondral ossification.

The primary center

In long bones, bone tissue first appears in the diaphysis (middle of shaft). Chondrocytes multiply and form trebeculae. Cartilage is progressively eroded and replaced by hardened bone, extending towards the epiphysis. A perichondrium layer surrounding the cartilage forms the periosteum, which generates osteogenic cells that then go on to make a collar that encircles the outside of the bone and remodels the medullary cavity on the inside.

The nutrient artery enters via the nutrient foramen from a small opening in the diaphysis. It invades the primary center of ossification, bringing osteogenic cells (osteoblasts on the outside, osteoclasts on the inside.) The canal of the nutrient foramen is directed away from more active end of bone when one end grows more than the other. When bone grows at same rate at both ends, the nutrient artery is perpendicular to the bone.

Most other bones (e.g. vertebrae) also have primary ossification centers, and bone is laid down in a similar manner.

Secondary centers

The secondary centers generally appear at the epiphysis. Secondary ossification mostly occurs after birth (except for distal femur and proximal tibia which occurs during 9th month of fetal development). The epiphyseal arteries and osteogenic cells invade the epiphysis, depositing osteoclasts and osteoblasts which erode the cartilage and build bone, respectively. This occurs at both ends of long bones but only one end of digits and ribs.

 
Microscopic image of the growth plate

Evolution

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A spotted gar larva at 22 days stained for cartilage (blue) and bone (red).

Several hypotheses have been proposed for how bone evolved as a structural element in vertebrates. One hypothesis is that bone developed from tissues that evolved to store minerals. Specifically, calcium-based minerals were stored in cartilage and bone was an exaptation development from this calcified cartilage.[5] However, other possibilities include bony tissue evolving as an osmotic barrier, or as a protective structure.

See also

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References

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  1. ^ "bone formation | Definition & Physiology". Encyclopedia Britannica. Retrieved 2021-01-22.
  2. ^ Caetano-Lopes J, Canhão H, Fonseca JE (2007). "Osteoblasts and bone formation". Acta reumatológica portuguesa. 32 (2): 103–10. PMID 17572649.
  3. ^ a b Emily Morey-Holton. "Predicting Height from the Length of Limb Bones". Examining Effects of Space Flight on the Skeletal System. Moffett Field, California: NASA Ames Research Center. Archived from the original on 2012-03-01.
  4. ^ Breeland, Grant; Sinkler, Margaret A.; Menezes, Ritesh G. (2024), "Embryology, Bone Ossification", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30969540, retrieved 2024-05-15
  5. ^ Donoghue PC, Sansom IJ (2002). "Origin and early evolution of vertebrate skeletonization". Microsc. Res. Tech. 59 (5): 352–72. doi:10.1002/jemt.10217. PMID 12430166. S2CID 10933086.