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Postnatal skeletal growth is driven by the epiphyseal stem cell niche: potential implications to pediatrics
Andrei S Chagin1,2, Phillip T Newton3,4
1Department of Physiology and Pharmacology, Karolinska Institutet, 17177, Stockholm, Sweden. andrei.chagin@ki.se.
Insights
Children
Area of Science:
- Skeletal Biology
- Developmental Biology
- Endocrinology
Background:
- Longitudinal bone growth in children relies on growth plates generating chondrocytes.
- Recent studies reveal stem cells and a stem cell niche within the growth plate.
- This niche emerges with the maturation of the secondary ossification center (SOC).
Purpose of the Study:
- To explore the distinct mechanisms of chondrocyte generation in neonatal versus postnatal growth.
- To discuss the implications of stem cell niche activity on longitudinal growth.
- To consider the influence of factors like estrogens, nutrition, and growth hormone.
Main Methods:
- Review and synthesis of recent findings on growth plate stem cells and niches.
- Comparative analysis of chondrocyte generation mechanisms across different developmental stages.
- Discussion of potential regulatory factors impacting longitudinal growth.
Main Results:
- Neonatal bone growth relies on chondro-progenitor consumption.
- Postnatal bone growth is driven by stem cell niche activity.
- The stem cell niche appears with SOC maturation into the epiphysis.
Conclusions:
- Chondrocyte generation mechanisms differ significantly between neonatal and postnatal periods.
- Stem cell niche activity is crucial for postnatal longitudinal bone growth.
- Estrogens, nutrition, and growth hormone may modulate these growth processes.
Abstract:
Children's longitudinal growth is facilitated by the activity of the growth plates, cartilage discs located near the ends of the long-bones. In order to elongate these bones, growth plates must continuously generate chondrocytes. Two recent studies have demonstrated that there are stem cells and a stem cell niche in the growth plate, which govern the generation of chondrocytes during the postnatal growth period. The niche, which allows stem cells to renew, appears at the same time as the secondary ossification center (SOC) matures into a bone epiphysis. Thus, the mechanism of chondrocyte generation differs substantially between neonatal and postnatal age, i.e., before and after the formation of the mineralized epiphyses. Hence, at the neonatal age bone growth is based on a consumption of chondro-progenitors whereas postnatally it is based on the activity of the stem cell niche. Here we discuss potential implications of these observations in relation to longitudinal growth, including the effects of estrogens, nutrition and growth hormone.
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