Syndecan-3: a cell-surface heparan sulfate proteoglycan important for chondrocyte proliferation and function during limb skeletogenesis

被引:41
作者
Pacifici, M [1 ]
Shimo, T
Gentili, C
Kirsch, T
Freeman, TA
Enomoto-Iwamoto, M
Iwamoto, M
Koyama, E
机构
[1] Thomas Jefferson Univ, Coll Med, Dept Orthopaed Surg, Philadelphia, PA 19107 USA
[2] Okayama Univ, Grad Sch Med & Dent, Dept Oral & Maxillofacial Surg, Okayama, Japan
[3] Ist Nazl Ric Canc, I-16132 Genoa, Italy
[4] Univ Maryland, Dept Orthopaed Surg, Baltimore, MD 21201 USA
关键词
syndecan-3; chondrocyte proliferation; Indian hedgehog; growth plate; chondrocyte maturation; limb skeletogenesis;
D O I
10.1007/s00774-004-0584-1
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Syndecans are single-pass integral membrane components that serve as co-receptors for growth factors and cytokines and can elicit signal transduction via their cytoplasmic tails. We review here previous studies from our groups on syndecan-3 biology and function in the growth plates of developing long bones in chick and mouse embryos. Gain- and loss-of-function data indicate that syndecan-3 has important roles in restricting mitotic activity to the proliferative zone of growth plate and may do so in close cooperation and interaction with the signaling molecule Indian hedgehog (IHH). Biochemical and protein-modeling data suggest a dimeric/oligomeric syndecan-3 configuration on the chondrocytes cell surface. Analyses of embryos misexpressing syndecan-3 or lacking IHH provide further clues on syndecan-3/IHH interdependence and interrelationships. The data and the conclusions reached provide insights into mechanisms fine-tuning chondrocyte proliferation, maturation, and function in the developing and growing skeleton and into how abnormalities in these fundamental mechanisms may subtend human congenital pathologies, including osteochondromas in hereditary multiple exostoses syndrome.
引用
收藏
页码:191 / 199
页数:9
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