Vannelli G B, Ensoli F, Zonefrati R, Kubota Y, Arcangeli A, Becchetti A, Camici G, Barni T, Thiele C J, Balboni G C
Department of Human Anatomy and Histology, University of Florence, Italy.
J Neurosci. 1995 Jun;15(6):4382-94. doi: 10.1523/JNEUROSCI.15-06-04382.1995.
Primary cell cultures from human fetal olfactory neuroepithelium have been isolated, cloned, and propagated in continuous in vitro culture for approximately 1 year. The two clones we report here synthesize both neuronal proteins and olfactory-specific markers as well as the putative olfactory neurotransmitter, carnosine. In addition, patchclamp experiments reveal that these cells are electrically excitable. Following exposure to a panel of aromatic chemicals one of the cell cultures shows a specific increase in intracellular cAMP, indicating that some degree of functional maturity is expressed in vitro. The results suggest that these cells originate from the "stem cell" compartment that gives rise to mature olfactory receptor neurons. These long-term cell cultures represent models that will be useful in studying the mechanism(s) of olfaction and the regulation of olfactory neurogenesis and differentiation.
已从人胎儿嗅神经上皮分离出原代细胞培养物,进行克隆,并在体外连续培养约1年。我们在此报告的两个克隆体既合成神经元蛋白和嗅觉特异性标志物,也合成假定的嗅觉神经递质肌肽。此外,膜片钳实验表明这些细胞具有电兴奋性。在接触一组芳香族化学物质后,其中一种细胞培养物显示细胞内cAMP有特异性增加,表明在体外表达了一定程度的功能成熟。结果表明这些细胞起源于产生成熟嗅觉受体神经元的“干细胞”区室。这些长期细胞培养物代表了有助于研究嗅觉机制以及嗅觉神经发生和分化调控的模型。