Department Plant Physiology, Sofia University 'St Kliment Ohridski', Sofia, Bulgaria.
Ann Bot. 2013 Feb;111(2):191-205. doi: 10.1093/aob/mcs264. Epub 2012 Dec 18.
Under stress-promoting conditions unicellular algae can undergo programmed cell death (PCD) but the mechanisms of algal cellular suicide are still poorly understood. In this work, the involvement of caspase-like proteases, DNA cleavage and the morphological occurrence of cell death in wasp venom mastoparan (MP)-treated Chlamydomonas reinhardtii were studied.
Algal cells were exposed to MP and cell death was analysed over time. Specific caspase inhibitors were employed to elucidate the possible role of caspase-like proteases. YVADase activity (presumably a vacuolar processing enzyme) was assayed by using a fluorogenic caspase-1 substrate. DNA breakdown was evaluated by DNA laddering and Comet analysis. Cellular morphology was examined by confocal laser scanning microscopy.
MP-treated C. reinhardtii cells expressed several features of necrosis (protoplast shrinkage) and vacuolar cell death (lytic vesicles, vacuolization, empty cell-walled corpse-containing remains of digested protoplast) sometimes within one single cell and in different individual cells. Nucleus compaction and DNA fragmentation were detected. YVADase activity was rapidly stimulated in response to MP but the early cell death was not inhibited by caspase inhibitors. At later time points, however, the caspase inhibitors were effective in cell-death suppression. Conditioned medium from MP-treated cells offered protection against MP-induced cell death.
In C. reinhardtii MP triggered PCD of atypical phenotype comprising features of vacuolar and necrotic cell deaths, reminiscent of the modality of hypersensitive response. It was assumed that depending on the physiological state and sensitivity of the cells to MP, the early cell-death phase might be not mediated by caspase-like enzymes, whereas later cell death may involve caspase-like-dependent proteolysis. The findings substantiate the hypothesis that, depending on the mode of induction and sensitivity of the cells, algal PCD may take different forms and proceed through different pathways.
在应激促进条件下,单细胞藻类可以经历程序性细胞死亡(PCD),但藻类细胞自杀的机制仍知之甚少。在这项工作中,研究了黄蜂毒液蜂毒素(MP)处理的莱茵衣藻中半胱氨酸蛋白酶样蛋白酶、DNA 切割和细胞死亡的形态发生的参与。
将藻类细胞暴露于 MP 中,并随时间分析细胞死亡。使用特定的半胱天冬酶抑制剂阐明半胱天冬酶样蛋白酶的可能作用。通过使用荧光半胱天冬酶-1底物测定 YVADase 活性(推测为液泡加工酶)。通过 DNA 梯状和彗星分析评估 DNA 断裂。通过共聚焦激光扫描显微镜检查细胞形态。
MP 处理的莱茵衣藻细胞表现出几种坏死特征(原生质体收缩)和液泡细胞死亡(溶酶体、液泡化、空细胞壁包含已消化原生质体残留物的尸体),有时在单个细胞内,有时在不同的单个细胞中。检测到核浓缩和 DNA 片段化。MP 处理后迅速刺激 YVADase 活性,但早期细胞死亡不受半胱天冬酶抑制剂抑制。然而,在稍后的时间点,半胱天冬酶抑制剂在抑制细胞死亡方面有效。来自 MP 处理细胞的条件培养基提供了对 MP 诱导的细胞死亡的保护。
在莱茵衣藻中,MP 触发了非典型表型的 PCD,其特征是液泡和坏死细胞死亡的特征,类似于过敏反应的模式。假设取决于细胞对 MP 的生理状态和敏感性,早期的细胞死亡阶段可能不由半胱天冬酶样酶介导,而晚期的细胞死亡可能涉及半胱天冬酶样依赖性蛋白水解。这些发现证实了这样的假设,即根据诱导方式和细胞的敏感性,藻类 PCD 可能采取不同的形式并通过不同的途径进行。