Rios-Barrera Daniel, Vega-Segura Alicia, Thibert Valerie, Rodríguez-Zavala Jose S, Torres-Marquez M Eugenia
Biochemistry Department, School of Medicine, UNAM, Apdo. Postal 70-159, 04510, Mexico D.F., Mexico.
Arch Microbiol. 2009 Jan;191(1):47-54. doi: 10.1007/s00203-008-0427-x. Epub 2008 Sep 2.
Living organisms are subject to stress, and among these stressors, heavy metals exposure triggers accumulation of sulfur metabolites. Among these metabolites, glutathione and phytochelatins are found in several organisms, such as Euglena gracilis. Pre-exposing E. gracilis to low concentrations of Hg2+ generates a population with resistance to even 0.2 mM Cd2+, and this resistance relies partly on phytochelatins. p38 MAPK is stimulated by stress and is involved in apoptotic as well as survival mechanisms. In this study, we explored its participation in heavy metal-induced stress and its possible role in sulfur metabolite accumulation. We found that about 51% of the E. gracilis pretreated with Hg2+ becomes resistant to Cd2+ and proliferates despite the presence of this metal. The accumulation of the sulfur metabolites gamma-glu-cys, glutathione and phytochelatin 2 displayed cyclic patterns that were disturbed by a challenge with Cd2+. We observed a p38 MAPK-like activity that was stimulated by acute or chronic heavy metal exposure, and its inhibition by SB203580 slightly diminished the accumulation of sulfur compounds. p38 MAPK inhibition also affected basal levels of glutathione in either pretreated or control cells. Thus, it appears that p38 MAPK mediates redox stress component of the signal pathway induced by heavy metals.
生物体会受到压力影响,在这些压力源中,重金属暴露会引发硫代谢物的积累。在这些代谢物中,谷胱甘肽和植物螯合肽在几种生物体中都有发现,比如纤细裸藻。将纤细裸藻预先暴露于低浓度的Hg2+会产生对高达0.2 mM Cd2+都有抗性的群体,这种抗性部分依赖于植物螯合肽。p38丝裂原活化蛋白激酶(p38 MAPK)会受到压力刺激,并参与凋亡以及生存机制。在本研究中,我们探究了其在重金属诱导的压力中的作用以及在硫代谢物积累中可能发挥的作用。我们发现,用Hg2+预处理的纤细裸藻中约51%对Cd2+产生抗性,并且即使存在这种金属也能增殖。硫代谢物γ-谷氨酰半胱氨酸、谷胱甘肽和植物螯合肽2的积累呈现出周期性模式,这些模式会因Cd2+的刺激而受到干扰。我们观察到一种类似p38 MAPK的活性,它会受到急性或慢性重金属暴露的刺激,用SB203580对其进行抑制会使硫化合物的积累略有减少。p38 MAPK抑制也会影响预处理细胞或对照细胞中谷胱甘肽的基础水平。因此,似乎p38 MAPK介导了重金属诱导的信号通路中的氧化还原应激成分。