Abstract
PURPOSE. The lamina cribrosa (LC) is a key site of damage in glaucomatous optic neuropathy. We previously found that glaucoma LC cells have an increased profibrotic gene expression, with mitochondrial dysfunction in the form of decreased mitochondrial membrane potential. Altered cell bioenergetics have recently been reported in organ fibrosis and in cancer. In this study, we carried out a systematic mitochondrial bioenergetic assessment and measured markers of alternative sources of cellular energy in normal and glaucoma LC cells. METHODS. LC cells from three glaucoma donors and three age-matched normal controls were assessed using VICTOR X4 Perkin Elmer (Waltham, MA) plate reader with different phosphorescent and luminescent probes. adenosine triphosphate levels, oxygen consumption rate, and extracellular acidification were measured and normalized to total protein content. RNA and protein expression levels of MCT1, MCT4, MTFHD2, and GLS2 were quantified using real-time RT-PCR and Western blotting. RESULTS. Glaucoma LC cells contain significantly less adenosine triphosphate (P
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Kamel, K., O’Brien, C. J., Zhdanov, A. V., Papkovsky, D. B., Clark, A. F., Stamer, D., & Irnaten, M. (2020). Reduced oxidative phosphorylation and increased glycolysis in human glaucoma lamina cribrosa cells. Investigative Ophthalmology and Visual Science, 61(13). https://doi.org/10.1167/IOVS.61.13.4
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