Endochondral ossification 

Section of fetal bone of cat. ir. Irruption of the subperiosteal tissue. p. Fibrous layer of the periosteum. o. Layer of osteoblasts. im. Subperiosteal bony deposit. (From Quain’s “Anatomy,” E. A. Schäfer.)
Section of fetal bone of cat. ir. Irruption of the subperiosteal tissue. p. Fibrous layer of the periosteum. o. Layer of osteoblasts. im. Subperiosteal bony deposit. (From Quain’s “Anatomy,” E. A. Schäfer.)

Endochondral ossification is one of the two processes during fetal development of the mammalian skeletal system in which bone tissue is created. It is also an essential process during the rudimentary formation of long bones, [1] the growth of the length of long bones, [2] and the healing of bone fractures. [3] Unlike intramembranous ossification, which is the other process, cartilage is present during endochondral ossification.

Contents

Growth of the cartilage model

The cartilage model would grow in length by continuous cell division of chondrocytes, which is accompanied by further secretion of extracellular matrix. This is called interstitial growth. The process of appositional growth occurs when the cartilage model would also grow in thickness which is due to the addition of more extracellular matrix on the periphery cartilage surface, which is accompanied by new chondroblasts that develop from the perichondrium.

Primary center of ossification

The first site of ossification occurs in the primary center of ossification, which is in the middle of diaphysis (shaft). The following steps then occur:

Secondary center of ossification

Cartilage is retained in the epiphyseal plate, located between the diaphysis (the shaft) and the epiphysis (end) of the bone. These areas of cartilage are known as secondary centers of ossification. Cartilage cells undergo the same transformation as above. As growth progresses, the proliferation of cartilage cells in the epiphyseal plate slows and eventually stops. The continuous replacement of cartilage by bone results in the obliteration of the epiphyseal plate, termed the closure of the epiphysis. Only articular cartilage remains. Mineralisation of articular cartilage and its replacement by bone continues in the adult, though at a much reduced rate than in growing animals.

Appositional bone growth

The growth in diameter of bones around the diaphysis occurs by deposition of bone beneath the periosteum. Osteoclasts in the interior cavity continue to degrade bone until its ultimate thickness is achieved, at which point the rate of formation on the outside and degradation from the inside is constant.

Histology

Part of a longitudinal section of the developing femur of a rabbit. a. Flattened cartilage cells. b. Enlarged cartilage cells. c, d. Newly formed bone. e. Osteoblasts. f. Giant cells or osteoclasts. g, h. Shrunken cartilage cells. (From “Atlas of Histology,” Klein and Noble Smith.)
Part of a longitudinal section of the developing femur of a rabbit. a. Flattened cartilage cells. b. Enlarged cartilage cells. c, d. Newly formed bone. e. Osteoblasts. f. Giant cells or osteoclasts. g, h. Shrunken cartilage cells. (From “Atlas of Histology,” Klein and Noble Smith.)

During endochondral ossification, four distinct zones can be seen at the light-microscope level.

  1. Zone of resting cartilage. This zone contains normal, resting hyaline cartilage.
  2. Zone of proliferation. In this zone, chondrocytes undergo rapid mitosis, forming distinctive looking stacks.
  3. Zone of maturation / hypertrophy. It is during this zone that the chondrocytes undergo hypertrophy (become enlarged). Chondrocytes contain large amounts of glycogen and begin to secrete alkaline phosphatase.
  4. Zone of calcification. In this zone, chondrocytes are either dying or dead, leaving cavities that will later become invaded by bone-forming cells. Chondrocytes here die when they can no longer receive nutrients or eliminate wastes via diffusion. This is because the calcified matrix is much less hydrated than hyaline cartilage.

References

  1. ^ Netter, Frank H. (1987), Musculoskeletal system: anatomy, physiology, and metabolic disorders. Summit, New Jersey: Ciba-Geigy Corporation ISBN 0914168886, p. 130: One exception is the clavicle.
  2. ^ Brighton, Carl T., Yoichi Sugioka, and Robert M. Hunt (1973), "Cytoplasmic structures of epiphyseal plate chondrocytes; quantitative evaluation using electron micrographs of rat costochondral junctions with specific reference to the fate of hypertrophic cells", Journal of Bone and Joint Surgery, 55-A: 771-784
  3. ^ Brighton, Carl T. and Robert M. Hunt (1986): "Histochemical localization of calcium in the fracture callus with potassium pyroantimonate: possible role of chondrocyte mitochondrial calcium in callus calcification", Journal of Bone and Joint Surgery, 68-A (5): 703-715

See also