International journal of molecular sciences · 2018
The Bacterial Protein CNF1 as a Potential Therapeutic Strategy against Mitochondrial Diseases: A Pilot Study.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Fabbri Alessia, Travaglione Sara, Maroccia Zaira, Guidotti Marco, Pierri Ciro Leonardo, Primiano Guido, Servidei Serenella, Loizzo Stefano, Fiorentini Carla
Аннотация
The Escherichia coli protein toxin cytotoxic necrotizing factor 1 (CNF1), which acts on the Rho GTPases that are key regulators of the actin cytoskeleton, is emerging as a potential therapeutic tool against certain neurological diseases characterized by cellular energy homeostasis impairment. In this brief communication, we show explorative results on the toxin’s effect on fibroblasts derived from a patient affected by myoclonic epilepsy with ragged-red fibers (MERRF) that carries a mutation in the m.8344A>G gene of mitochondrial DNA. We found that, in the patient’s cells, besides rescuing the wild-type-like mitochondrial morphology, CNF1 administration is able to trigger a significant increase in cellular content of ATP and of the mitochondrial outer membrane marker Tom20. These results were accompanied by a profound F-actin reorganization in MERRF fibroblasts, which is a typical CNF1-induced effect on cell cytoskeleton. These results point at a possible role of the actin organization in preventing or limiting the cell damage due to mitochondrial impairment and at CNF1 treatment as a possible novel strategy against mitochondrial diseases still without cure.
Предметные рубрики MeSH
Adenosine TriphosphateBacterial ToxinsDNA, MitochondrialElectron Transport Complex IVEscherichia coliEscherichia coli ProteinsFibroblastsGene ExpressionHumansMERRF SyndromeMaleMembrane Transport ProteinsMiddle AgedMitochondriaMitochondrial Precursor Protein Import Complex ProteinsMutationPilot ProjectsPrimary Cell CultureReceptors, Cell SurfaceStress Fibers