The 7D4, 4C3 and 3B3 (-) Chondroitin Sulphation Motifs are expressed at Sites of Cartilage and Bone Morphogenesis during Foetal Human Knee Joint Development

J. Melrose, Susan M. Smith, C. Hughes, C. Little, B. Caterson, A. Hayes
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引用次数: 6

Abstract

Novel sulphation motifs within the glycosaminoglycan (GAG) chain structure of chondroitin sulphate (CS)- containing s are associated with sites of growth and differentiation in many biological systems where they function as molecular recognition sites involved in the binding, sequestration or presentation of soluble signalling molecules (e.g. growth factors, cytokines, morphogens). The specific sulphation motifs on CS identified by monoclonal antibodies 3-B-3(-), 4-C-3 and 7-D-4 are also associated with distinct cohorts of cells in areas of tissue morphogenesis in human foetal knee joint development. We hypothesize that such motifs may have roles to play in the regulation of proliferative/differentiative events during tissue morphogenesis. In the present investigation we have examined the distribution of these CS motifs within the rudiment cartilage, stromal connective tissues surrounding the rudiment cartilages and developing growth plates of the human foetal knee joint. These CS motifs had broad, overlapping distributions throughout the differentiating connective tissues undergoing morphogenesis and after joint cavitation were localised very specifically to the rudiment cartilage destined to form the permanent articular cartilage postnatally, and to the terminally differentiated chondrocytes and calcified cartilage-bone interface in the growth plate cartilages. The overlapping distributions of these molecules within the presumptive articular cartilage, prior to secondary ossification, suggests that they participate in early signalling events involved in tissue development and indicates that the cells within this zone are phenotypically distinct from those of the underlying rudiment cartilage.
7D4、4C3和3B3(-)软骨素硫酸基序在胎儿膝关节发育过程中软骨和骨形态发生部位表达
含有硫酸软骨素(CS)的糖胺聚糖(GAG)链结构中的新型硫酸基序与许多生物系统中的生长和分化位点有关,在这些位点中,它们作为分子识别位点参与可溶性信号分子(如生长因子、细胞因子、形态因子)的结合、隔离或呈现。通过单克隆抗体3-B-3(-)、4-C-3和7-D-4鉴定出的CS上的特定硫酸基序也与人类胎儿膝关节发育中组织形态发生区域的不同细胞群有关。我们假设这些基序可能在组织形态发生过程中对增殖/分化事件的调节中发挥作用。在目前的研究中,我们研究了这些CS基序在人类胎儿膝关节的初级软骨、初级软骨周围的基质结缔组织和发育中的生长板中的分布。这些CS基元在形态发生和关节空化后的分化结缔组织中具有广泛的重叠分布,非常具体地定位于注定在出生后形成永久关节软骨的雏形软骨,以及生长板软骨中终末分化的软骨细胞和钙化的软骨-骨界面。在继发性骨化之前,这些分子在假定的关节软骨内的重叠分布表明,它们参与了组织发育的早期信号事件,并表明该区域内的细胞在表型上与潜在的原始软骨不同。
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