Domowicz Miriam S, Mangoura Dimitra, Schwartz Nancy B
Departments of Pediatrics and Biochemistry & Molecular Biology, Committee on Developmental Biology, The University of Chicago, 5841 S. Maryland Avenue, MC 5058, Chicago, IL 60637, USA.
Brain Res Dev Brain Res. 2003 Jul 12;143(2):207-16. doi: 10.1016/s0165-3806(03)00133-0.
Proteoglycans have been suggested to play roles in pattern formation in the developing central nervous system. In the chick embryo, aggrecan, a chondroitin sulfate proteoglycan, has a regionally-specific and developmentally-regulated expression profile. Telencephalic neuronal cultures, when aggregated, exhibit aggrecan expression patterns comparable to those observed in vivo. The chicken mutation nanomelia produces a truncated aggrecan species that cannot be processed further and is not secreted. Neurons from normal and nanomelic chick embryo telencephalon were scored for aggregate formation and analyzed for distribution of aggrecan protein and expression of aggrecan mRNA. Distinctly different pattern formation, with respect to aggregate size (smaller) and number (fewer) were observed in poly-L-lysine plated neuronal cultures derived from nanomelic embryos when compared to those derived from normal embryos. Significantly, the nanomelic phenotype was subsequently rescued upon addition of the brain-specific form of aggrecan. Modulation of neuronal aggregate formation was mimicked by treatment with chondroitinase ABC but not other glycanases, and was rescued by addition of chondroitin 6-sulfate to the culture media. Lastly, although broad and diffuse distribution of aggrecan among the cell aggregates in the culture paradigm was observed by immunocytochemistry, mRNA in situ hybridization revealed that only a small population of cells in the center of the aggregates was responsible for the production of the secreted aggrecan found associated with neuronal aggregates. These studies suggest a function for aggrecan as a diffusible signal in CNS histomorphogenesis.
蛋白聚糖被认为在发育中的中枢神经系统的模式形成中发挥作用。在鸡胚中,硫酸软骨素蛋白聚糖聚集蛋白聚糖具有区域特异性和发育调控的表达谱。端脑神经元培养物聚集时,会表现出与体内观察到的聚集蛋白聚糖表达模式相当的模式。鸡的纳米肢突变产生一种截短的聚集蛋白聚糖物种,该物种无法进一步加工且不会分泌。对来自正常和纳米肢鸡胚端脑的神经元进行聚集形成评分,并分析聚集蛋白聚糖蛋白的分布和聚集蛋白聚糖mRNA的表达。与来自正常胚胎的神经元培养物相比,在来自纳米肢胚胎的聚-L-赖氨酸包被的神经元培养物中观察到明显不同的模式形成,在聚集大小(更小)和数量(更少)方面。重要的是,在添加脑特异性形式的聚集蛋白聚糖后,纳米肢表型随后得到挽救。用硫酸软骨素酶ABC处理可模拟神经元聚集形成的调节,但其他聚糖酶则不能,并且通过向培养基中添加硫酸软骨素6-硫酸盐可挽救这种调节。最后,尽管通过免疫细胞化学观察到聚集蛋白聚糖在培养模式中的细胞聚集体中广泛且弥散分布,但mRNA原位杂交显示,聚集体中心只有一小部分细胞负责产生与神经元聚集体相关的分泌型聚集蛋白聚糖。这些研究表明聚集蛋白聚糖在中枢神经系统组织形态发生中作为一种可扩散信号发挥作用。