کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1984480 1539942 2010 19 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Distinctions and similarities of cell bioenergetics and the role of mitochondria in hypoxia, cancer, and embryonic development
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Distinctions and similarities of cell bioenergetics and the role of mitochondria in hypoxia, cancer, and embryonic development
چکیده انگلیسی

In this review we compare situations under which the major cellular role of mitochondria, oxidative phosphorylation (OXPHOS), is transiently suppressed. Two types of cellular bioenergetics exist, related to the predominance of glycolysis either disconnected or fully connected to OXPHOS: i) “glycolytic” phenotype, when the glycolytic end-product pyruvate is marginally used for OXPHOS; and, ii) OXPHOS phenotype with fully developed and active OXPHOS machinery consuming all pyruvate. A switch to glycolytic phenotype is typically orchestrated by gene reprogramming due to AMP-activated protein kinase, hypoxia-induced factor (HIF), NFκB, mTOR, and by oncogenes. At normoxia a continuous hydroxylation of HIF1α prolines by prolyl hydroxylase domain enzymes (PHDs) and asparagines by factor-inhibiting HIF (FIH) occurs, resulting in HIF1α polyubiquitination/degradation. With O2 below a threshold level (<5% O2) cytosolic H2O2 raises and oxidizes Fe2+ of PHDs and FIH, inactivates them, thus stabilizing HIFα and upregulating transcription of specific genes. The source of H2O2 burst (not manifested in isolated mitochondria) is the respiratory chain Complex III QO site. Frequently hypoxic microenvironment of malignant tumors stimulates HIF-mediated conversion to the glycolytic state, nevertheless OXPHOS tumors also exist. The glycolytic mode predominates prior to implantation phase of embryonic development, hence in embryonic stem cells. Finally, a “Poderoso hypothesis” is discussed, predicting repetitive conversions to a transient glycolytic mode after a meal and concomitant insulin signaling. Accordingly, insulin stimulates mitochondrial NO synthase simultaneously with cellular glucose intake. The elevated NO diminishes respiration by inhibiting cytochrome c oxidase. Type 2 diabetes may result from the accumulated impact of such nitrosative/oxidative stress.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: The International Journal of Biochemistry & Cell Biology - Volume 42, Issue 5, May 2010, Pages 604–622
نویسندگان
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