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Updated: Aug 13, 2026

Culturing and Measuring Fetal and Newborn Murine Long Bones
Published on: April 26, 2019
[Growth plate structure of the vertebral body in children of different age groups]
Insights
This study details how the growth plate (GP) in children
Area of Science:
- Developmental Biology
- Histology
- Biochemistry
Context:
- The postnatal development of the vertebral growth plate (GP) is crucial for spinal growth.
- Understanding age-related structural and cellular changes in the GP is essential for pediatric orthopedics and developmental studies.
Purpose:
- To investigate the formation and function of vertebral growth plate structural components in children.
- To analyze age-specific changes in cells and extracellular matrix within the vertebral growth plate (GP) from newborns to adolescents.
Summary:
- Detailed histological, histochemical, and electron microscopic analyses were performed on vertebral growth plate (GP) samples from children aged 0 to 14 years.
- The study describes chondrogenic differentiation, including cellular changes from chondroblasts to chondrocytes and matrix production.
- Age-related alterations in cell distribution, proliferation, and matrix composition within the vertebral growth plate (GP) were characterized.
Impact:
- Provides a comprehensive understanding of vertebral growth plate (GP) development and cellular dynamics.
- Offers insights into the biological basis of spinal growth and potential mechanisms underlying growth disturbances.
Abstract:
The purpose of this study was to investigate the regularities of formation and functioning of the structural components of the growth plate (GP) of the vertebral body in children during the postnatal period of ontogenesis: in newborns and in children aged 1, 3-5- 6-10- and 12-14-years. GP samples of were studied using histological, histochemical (demonstration of oxidation-reduction enzyme activity, polysaccharides, glycosaminoglycans) and electron microscopic methods with special reference to the age changes of the cells and matrix in different GP zones of the vertebral body. The process of chondrogenic differentiation is described, which includes the successive stages of cellular modifications starting from an undifferentiated chondroblast through a highly differentiated chondrocyte to a degrading and dying chondrocyte. The changes in synthetic activity of cartilage cells are noted as well as the nature of matrix components that are produced by them in the course of differentiation. Regular age-related changes of spatial distribution of mitotically active cells, forming cellular columns, and of isogenous groups are characterized in relation to the alterations of matrix quantity and chemical content in GP of the vertebral body.
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