Hayes A J, Dowthwaite G P, Webster S V, Archer C W
Cardiff School of Biosciences, Cardiff University, PO Box 911 Museum Avenue, Cardiff, UK.
J Anat. 2003 Jun;202(6):495-502. doi: 10.1046/j.1469-7580.2003.00185.x.
We examined the distribution of Notch family members and their ligands during the development of articular cartilage and the growth plate. Notch 1 was expressed by the chondrocytes of the developing articular surface but became increasingly restricted to the deeper layers after birth whilst expression of this family member was restricted to hypertrophic chondrocytes in the growth plate. Notch 2 and 4, Delta and Jagged 2 showed a broadly similar distribution, being present throughout the articular cartilage during development and becoming increasingly restricted to deeper layers with age. Hypertrophic chondrocytes within the growth plate also expressed Notch 2 and 4, Delta and Jagged 2 (which was also expressed in prehypertrophs). Notch 3 and Jagged 1 were absent from developing articular cartilage but were present in deeper layers at later time points (> 1 month) and both receptor and ligand were expressed in hypertrophic chondrocytes at all ages examined. These results highlight the complex Notch signalling interactions that result in the formation of the heterogeneous articular cartilage and allow for the co-ordinated ossification and elongation of the growth plate. Mechanisms by which these processes are controlled are discussed in light of recent advances in the understanding of Notch signalling pathways.
我们研究了Notch家族成员及其配体在关节软骨和生长板发育过程中的分布情况。Notch 1在发育中的关节表面软骨细胞中表达,但出生后逐渐局限于更深层,而该家族成员在生长板中仅限于肥大软骨细胞表达。Notch 2和4、Delta和Jagged 2呈现出大致相似的分布,在发育过程中存在于整个关节软骨中,并随着年龄增长逐渐局限于更深层。生长板内的肥大软骨细胞也表达Notch 2和4、Delta和Jagged 2(在肥大前软骨细胞中也有表达)。Notch 3和Jagged 1在发育中的关节软骨中不存在,但在后期时间点(>1个月)出现在更深层,并且在所检测的所有年龄段的肥大软骨细胞中受体和配体均有表达。这些结果突出了复杂的Notch信号相互作用,其导致了异质性关节软骨的形成,并允许生长板的协调骨化和延长。鉴于对Notch信号通路理解的最新进展,讨论了控制这些过程的机制。