کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6021484 | 1580642 | 2015 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patients
ترجمه فارسی عنوان
اختلالات آهن و اختلالات انرژی میتوکندری، فیبروبلاست ها و نورون های القا شده را از بیماران مبتلا به نوروژنز وابسته به پانتانت کیناز تشخیص می دهد
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کلمات کلیدی
PIHDHR-123IRP1PANK2PKANTMRMNBIARPAdichlorofluoresceinLIPDFODeferoxamineDcfINSFACROS - ROSFerric Ammonium Citrate - آهن آمونیوم سیتراتLabile iron pool - استخر چربneurodegeneration with brain iron accumulation - ایجاد عصبی با تجمع آهن مغزdihydrorhodamine 123 - دی هیدرو رودامین 123Iron metabolism - متابولیسم آهنtetramethylrhodamine methyl ester - متیل استر تترامتیل رودامینMitochondria - میتوکندریاInduced Neurons - نورونهای تحریک شدهIron regulatory protein 1 - پروتئین تنظیم کننده آهن 1Pyridoxal isonicotinoyl hydrazone - پییریدکسال ایزونیکوتینویل هیدرازونReactive oxygen species - گونههای فعال اکسیژن
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
عصب شناسی
چکیده انگلیسی
Pantothenate kinase-associated neurodegeneration is an early onset autosomal recessive movement disorder caused by mutation of the pantothenate kinase-2 gene, which encodes a mitochondrial enzyme involved in coenzyme A synthesis. The disorder is characterised by high iron levels in the brain, although the pathological mechanism leading to this accumulation is unknown. To address this question, we tested primary skin fibroblasts from three patients and three healthy subjects, as well as neurons induced by direct fibroblast reprogramming, for oxidative status, mitochondrial functionality and iron parameters. The patients' fibroblasts showed altered oxidative status, reduced antioxidant defence, and impaired cytosolic and mitochondrial aconitase activities compared to control cells. Mitochondrial iron homeostasis and functionality analysis of patient fibroblasts indicated increased labile iron pool content and reactive oxygen species development, altered mitochondrial shape, decreased membrane potential and reduced ATP levels. Furthermore, analysis of induced neurons, performed at a single cell level, confirmed some of the results obtained in fibroblasts, indicating an altered oxidative status and signs of mitochondrial dysfunction, possibly due to iron mishandling. Thus, for the first time, altered biological processes have been identified in vitro in live diseased neurons. Moreover, the obtained induced neurons can be considered a suitable human neuronal model for the identification of candidate therapeutic compounds for this disease.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neurobiology of Disease - Volume 81, September 2015, Pages 144-153
Journal: Neurobiology of Disease - Volume 81, September 2015, Pages 144-153
نویسندگان
Paolo Santambrogio, Sabrina Dusi, Michela Guaraldo, Luisa Ida Rotundo, Vania Broccoli, Barbara Garavaglia, Valeria Tiranti, Sonia Levi,