Zuppini Anna, Baldan Barbara, Millioni Renato, Favaron Francesco, Navazio Lorella, Mariani Paola
Dipartimento di Biologia, Università di Padova, via U. Bassi 58/B, 35131 Padova, Italy.
Dipartimento Te. S.A.F., Sez. Patologia Vegetale, Università di Padova, str. Romea 16, 35020 Legnaro, Padova, Italy.
New Phytol. 2004 Feb;161(2):557-568. doi: 10.1046/j.1469-8137.2003.00969.x. Epub 2003 Dec 9.
• Chitosan, a component of the cell wall of many fungi, has been widely used to mimic pathogen attack and has been shown to induce several defence responses. • Here we show that low concentrations (50 µg ml ) of chitosan are able to induce an increase in cytosolic Ca concentration ([Ca ] ), accumulation of H O in the culture medium, induction of the defence gene chalcone synthase (chs), and cell death in soybean cells (Glycine max). • Chitosan-induced cell death occurred through cytoplasmic shrinkage, chromatin condensation and activation of caspase 3-like protease, suggesting the activation of a programmed cell death (PCD) pathway. Buffering extracellular Ca with the Ca chelator EGTA prevents [Ca ] elevation, H O production and all downstream PCD features, but not cell death. • Higher doses (200 µg ml ) of chitosan evoked neither Ca transient and H O production nor caspase 3-like activation, but caused cell death, possibly as a result of plasma membrane disturbance.
• 壳聚糖是许多真菌细胞壁的一种成分,已被广泛用于模拟病原体攻击,并已显示能诱导多种防御反应。
• 在此我们表明,低浓度(50微克/毫升)的壳聚糖能够诱导大豆细胞(大豆)胞质钙浓度([Ca])升高、培养基中H₂O积累、防御基因查尔酮合酶(chs)的诱导以及细胞死亡。
• 壳聚糖诱导的细胞死亡通过细胞质收缩、染色质浓缩和类半胱天冬酶3蛋白酶的激活而发生,表明程序性细胞死亡(PCD)途径被激活。用钙螯合剂EGTA缓冲细胞外钙可防止[Ca]升高、H₂O产生以及所有下游PCD特征,但不能防止细胞死亡。
• 更高剂量(200微克/毫升)的壳聚糖既不引起钙瞬变和H₂O产生,也不引起类半胱天冬酶3样激活,但会导致细胞死亡,这可能是由于质膜扰动所致。