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壳聚糖诱导大豆细胞中钙介导的程序性细胞死亡。

Chitosan induces Ca -mediated programmed cell death in soybean cells.

作者信息

Zuppini Anna, Baldan Barbara, Millioni Renato, Favaron Francesco, Navazio Lorella, Mariani Paola

机构信息

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.

出版信息

New Phytol. 2004 Feb;161(2):557-568. doi: 10.1046/j.1469-8137.2003.00969.x. Epub 2003 Dec 9.

Abstract

•  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.

摘要

• 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。

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