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质膜辅酶Q在细胞凋亡调控中的作用。

Role of plasma membrane coenzyme Q on the regulation of apoptosis.

作者信息

López-Lluch G, Barroso M P, Martín S F, Fernández-Ayala D J, Gómez-Díaz C, Villalba J M, Navas P

机构信息

Laboratorio Andaluz de Biología, Universidad Pablo de Olavide, Sevilla, Spain.

出版信息

Biofactors. 1999;9(2-4):171-7. doi: 10.1002/biof.5520090212.

Abstract

Serum withdrawal is a model to study the mechanisms involved in the induction of apoptosis caused by mild oxidative stress. Apoptosis induced by growth factors removal was prevented by the external addition of antioxidants such as ascorbate, alpha-tocopherol and coenzyme Q (CoQ). CoQ is a lipophilic antioxidant which prevents oxidative stress and participates in the regeneration of alpha-tocopherol and ascorbate in the plasma membrane. We have found an inverse relationship between CoQ content in plasma membrane and lipid peroxidation rates in leukaemic cells. CoQ10 addition to serum-free culture media prevented both lipid peroxidation and cell death. Also, CoQ10 addition decreased ceramide release after serum withdrawal by inhibition of magnesium-dependent plasma membrane neutral-sphingomyelinase. Moreover, CoQ10 addition partially blocked activation of CPP32/caspase-3. These results suggest CoQ of the plasma membrane as a regulator of initiation phase of oxidative stress-mediated serum withdrawal-induced apoptosis.

摘要

血清撤除是一种用于研究轻度氧化应激诱导细胞凋亡机制的模型。通过外部添加抗氧化剂如抗坏血酸、α-生育酚和辅酶Q(CoQ),可防止因生长因子去除而诱导的细胞凋亡。CoQ是一种亲脂性抗氧化剂,可防止氧化应激并参与质膜中α-生育酚和抗坏血酸的再生。我们发现白血病细胞质膜中的CoQ含量与脂质过氧化速率呈负相关。向无血清培养基中添加CoQ10可防止脂质过氧化和细胞死亡。此外,添加CoQ10可通过抑制镁依赖性质膜中性鞘磷脂酶来减少血清撤除后的神经酰胺释放。此外,添加CoQ10可部分阻断CPP32/半胱天冬酶-3的激活。这些结果表明质膜中的CoQ作为氧化应激介导的血清撤除诱导细胞凋亡起始阶段的调节剂。

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