Related Experiment Video
Updated: Aug 5, 2026

Culture of Murine Embryonic Metatarsals: A Physiological Model of Endochondral Ossification
Published on: December 3, 2016
Weight loading young chicks inhibits bone elongation and promotes growth plate ossification and vascularization
1Institute of Animal Science, the Volcani Center, Bet Dagan, The Hebrew Univ. of Jerusalem, Rehovot, Israel.
Insights
Weight loading on young chicks during growth reduced long bone length and diameter by narrowing growth plates. This mechanical stress increased mineralization and altered gene expression, accelerating bone development.
Area of Science:
- Biomechanical Engineering
- Developmental Biology
- Orthopedic Research
Background:
- Mechanical stimuli are crucial for adult bone remodeling, but their impact on developing bone is less understood.
- Weight loading's effects on the growth plates of young animals require further investigation.
Purpose of the Study:
- To investigate the effects of mechanical weight loading on the growth plates and long bone development in young chicks.
- To elucidate the molecular mechanisms underlying load-induced bone growth modulation.
Main Methods:
- Chicks were subjected to external weight loading (10% body weight) during their rapid growth phase.
- Analysis included bone morphometry, growth plate width and mineralization assessment, Northern blot, in situ hybridization, and gene expression analysis (OPN, MMP9, MMP13).
Main Results:
- Weight loading significantly reduced long bone length and diameter, with growth plates being narrower (75% of controls) and more mineralized.
- Mechanically loaded growth plates showed altered expression zones for collagen types II and X, increased osteopontin (OPN) expression, and enhanced expression of matrix metalloproteinases (MMPs) MMP9 and MMP13.
- Increased vascularization into the growth plates was observed in the loaded group.
Conclusions:
- Mechanical strain on growth plate chondrocytes induces overexpression of OPN, MMP9, and MMP13.
- These molecular changes facilitate blood vessel penetration, cartilage resorption, and ossification, leading to shorter bones and narrower growth plates.
- Weight loading accelerates developmental ossification in young bone through specific molecular signaling pathways.
Abstract:
The mechanical stimuli resulting from weight loading play an important role in mature bone remodeling. However, the effect of weight loading on the developmental process in young bones is less well understood. In this work, chicks were loaded with bags weighing 10% of their body weight during their rapid growth phase. The increased load reduced the length and diameter of the long bones. The average width of the bag-loaded group's growth plates was 75 +/- 4% that of the controls, and the plates showed increased mineralization. Northern blot analysis, in situ hybridization, and longitudinal cell counting of mechanically loaded growth plates showed narrowed expression zones of collagen types II and X compared with controls, with no differences between the relative proportions of those areas. An increase in osteopontin (OPN) expression with loading was most pronounced at the bone-cartilage interface. This extended expression overlapped with tartarate-resistant acid phosphatase staining and with the front of the mineralized matrix in the chondro-osseous junction. Moreover, weight loading enhanced the penetration of blood vessels into the growth plates and enhanced the gene expression of the matrix metalloproteinases MMP9 and MMP13 in those growth plates. On the basis of these results, we speculate that the mechanical strain on the chondrocytes in the growth plate causes overexpression of OPN, MMP9, and MMP13. The MMPs enable penetration of the blood vessels, which carry osteoclasts and osteoblasts. OPN recruits the osteoclasts to the cartilage-bone border, thus accelerating cartilage resorption in this zone and subsequent ossification which, in turn, contributes to the observed phenotype of narrower growth plate and shorter bones.
Related Concept Videos
Growth of Cartilage and Bone Tissue
Bone Formation by Intramembranous Ossification
The process begins when mesenchymal cells in the embryonic skeleton gather together and differentiate into osteogenic cells, which then develop into...
Bone Disorders
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...
Hormones and Bone Tissue
Hormones That Influence Osteoblasts and/or Maintain the Matrix
Several hormones are necessary for controlling bone growth and maintaining the bone matrix. The pituitary gland secretes growth hormone (GH), which, as its name implies, controls bone growth. This happens in several ways: first, it triggers chondrocyte...
Changes in the Appendicular Skeleton with Age
Initially, the limb buds consist of a core of mesenchyme covered by a layer of ectoderm. The ectoderm at the end of the limb bud thickens to form a narrow crest called the apical ectodermal ridge. This ridge stimulates the underlying...
Bone Formation by Endochondral Ossification

