Downie S A, Newman S A
Department of Cell Biology and Anatomy, New York Medical College, Valhalla 10595, USA.
Dev Biol. 1995 Dec;172(2):519-30. doi: 10.1006/dbio.1995.8068.
Fibronectin expression and spatiotemporal distribution were examined in relation to the distinctive patterns of mesenchymal condensation and chondrogenesis seen in high-density serum-free cultures of chicken wing and leg bud precartilage cells. More fibronectin protein was produced on a per cell basis by leg than by wing mesenchyme, both in freshly isolated tissue and during the prechondrogenic condensation period in culture, where the difference was twofold. The quantitative difference in fibronectin expression in freshly isolated wing and leg mesenchyme was also seen at the level of total and poly (A)+ RNA. During the condensation phase, fibronectin was distributed in the wing and leg mesenchymal cultures in a way that prefigured the eventual distribution of cartilage in these cultures: in wing cultures condensations were broad and flat, and rich in diffusely organized fibronectin; in leg cultures, condensations were compact and spheroidal, and contained abundant deposits of fibronectin. In addition, the leg condensations were connected by long fibronectin-rich fibers. Transient treatment with TGF-beta early during the culture period led to increase in fibronectin production and expansion of condensations in both wing and leg cultures. Leg mesenchyme was more responsive to transforming growth factor-beta than wing mesenchyme with respect to fibronectin production, and this was reflected in a greater enhancement of cartilage formation in later cultures. Treatment of cultures with monoclonal antibody 304 directed against the amino-terminal heparin-binding domain of fibronectin inhibited condensation formation and reduced chondrogenesis in wing mesenchyme, but left these two processes unchanged in leg mesenchyme, despite disruption by the antibody of the leg-specific fibronectin fibers. These studies indicate that for both wing and leg mesenchyme the morphology, extent, and spatiotemporal regulation of precartilage condensation and subsequent chondrogenesis closely parallels the deposition of fibronectin. But whereas the interaction between cells and fibronectin in wing bud mesenchyme is mediated in part by the protein's amino-terminal domain, this domain does not appear to be involved in analogous interactions in leg bud mesenchyme.
研究了纤连蛋白的表达及其时空分布,以探讨鸡翅和鸡腿芽前软骨细胞高密度无血清培养中所见的间充质凝聚和软骨形成的独特模式。无论是在新鲜分离的组织中,还是在培养的软骨形成前期凝聚阶段,每个细胞产生的纤连蛋白蛋白量,腿部间充质都比翅膀间充质多,两者相差两倍。在总RNA和聚腺苷酸加尾RNA水平上,也观察到新鲜分离的翅膀和腿部间充质中纤连蛋白表达的定量差异。在凝聚阶段,纤连蛋白在翅膀和腿部间充质培养物中的分布方式预示了软骨在这些培养物中的最终分布:在翅膀培养物中,凝聚物宽而扁平,富含分散组织的纤连蛋白;在腿部培养物中,凝聚物紧凑且呈球形,含有大量纤连蛋白沉积物。此外,腿部凝聚物由富含纤连蛋白的长纤维连接。在培养期早期用转化生长因子-β进行短暂处理,导致翅膀和腿部培养物中纤连蛋白产生增加以及凝聚物扩大。就纤连蛋白产生而言,腿部间充质比翅膀间充质对转化生长因子-β更敏感,这反映在后期培养中软骨形成的更大增强上。用针对纤连蛋白氨基末端肝素结合域的单克隆抗体304处理培养物,可抑制翅膀间充质中的凝聚物形成并减少软骨形成,但对腿部间充质中的这两个过程没有影响,尽管该抗体破坏了腿部特异性的纤连蛋白纤维。这些研究表明,对于翅膀和腿部间充质来说,前软骨凝聚和随后软骨形成的形态、范围和时空调节与纤连蛋白的沉积密切平行。但是,翅膀芽间充质中细胞与纤连蛋白之间的相互作用部分是由该蛋白的氨基末端结构域介导的,而该结构域似乎不参与腿部芽间充质中的类似相互作用。