OXIDATIVE DNA DAMAGE & OXYSTEROL INDUCED APOPTOSIS

本子项目是利用由NIH/NCRR资助的中心赠款提供的资源的众多研究子项目之一。子项目和研究者（PI）可能已经从另一个NIH来源获得了主要资金，因此可以在其他CRISP条目中表示。列出的机构是中心的，不一定是研究者的机构。本项目的主要目的是研究线粒体在氧甾醇诱导的人淋巴细胞白血病细胞凋亡中的作用。在各种细胞类型中，特别是白血病淋巴样细胞中，氧甾醇是一类有效的细胞凋亡诱导剂。氧化甾醇还作为参与胆固醇生物合成、细胞生长和凋亡的基因的强大转录调节剂。虽然氧甾醇诱导淋巴样细胞凋亡的分子基础尚不清楚，但一些研究表明，氧甾醇诱导细胞凋亡是通过活性氧生成介导的。在上一个资助周期中获得的结果表明，氧化甾醇处理CEM细胞会导致ATP水平下降和线粒体膜电位丧失。该项目将验证活性氧损伤，特别是线粒体DNA损伤在氧甾醇诱导的人类白血病细胞凋亡中起作用的假设。我们的假设预测线粒体DNA的氧化损伤可导致线粒体功能障碍和诱导细胞凋亡。为了验证这一假设，我们将：1)确定暴露于氧甾醇后，对氧甾醇敏感的人淋巴细胞的细胞核和线粒体DNA氧化损伤的形成和修复是否高于对氧甾醇抗性的细胞；2)确定暴露于氧甾醇后，对氧甾醇敏感和抗性的人淋巴细胞的线粒体功能和功能障碍；3)确定氧化应激相关基因的表达谱。氧甾醇诱导淋巴样细胞凋亡过程中的DNA修复与凋亡。该项目将有助于为一个旨在了解线粒体在细胞凋亡过程中的作用的研究项目奠定基础。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The major objective of this project is to study the role of mitochondria in oxysterol-induced apoptosis of human lymphoblastic leukemia cells. Oxysterols represent a class of potent inducers of apoptosis in various cell types, particularly leukemic lymphoid cells. Oxysterols also act as powerful transcriptional regulators of genes involved in cholesterol biosynthesis, cell growth and apoptosis. Although the molecular basis of oxysterol-induced apoptosis of lymphoid cells remains unknown, some studies have suggested that oxysterol induction of apoptosis is mediated by reactive oxygen species generation. Results obtained in the previous funding cycle show that oxysterol treatment of CEM cells induces a decrease in ATP levels and loss of mitochondrial membrane potential. This project will test the hypothesis that ROS damage particularly to mitochondrial DNA plays a role in oxysterol-induced apoptosis of human leukemia cells. Our hypothesis predicts that oxidative damage to mitochondrial DNA can lead to mitochondrial dysfunction and induction of apoptosis. To test this hypothesis we will: 1) determine whether the formation and repair of oxidative damage to nuclear and mitochondrial DNA are higher in oxysterol sensitive human lymphoid cells than in oxysterol-resistant cells after exposure to oxysterols, 2) determine mitochondrial function and dysfunction in oxysterol-sensitive and resistant human lymphoid cells after exposure to oxysterols, and 3) determine the expression profile of genes involved in oxidative stress, DNA repair and apoptosis during oxysterol-induced apoptosis of lymphoid cells. This project will assist in laying the foundation for a research project directed towards the understanding of the role of mitochondria in the process of apoptosis.