Parasitology international · 2006
The effect of TAO expression on PCD-like phenomenon development and drug resistance in Trypanosoma brucei.
СтатьяНазвание 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.
Tsuda Akiko, Witola William H, Konnai Satoru, Ohashi Kazuhiko, Onuma Misao
Аннотация
Drug resistance in Trypanosoma brucei causes severe problems for people and domestic animals, but molecular mechanisms of the resistance are not well known. Programmed cell death (PCD) is a fundamental process in both multicellular and unicellular organisms, and it is speculated to be one of the important factors contributing to the emergence of drug resistance. We have previously reported that the expression of TAO appears to play a role in the inhibition of the PCD-like phenomenon development in T. brucei. In this study, to ascertain the correlation between the development of the PCD-like phenomenon and the expression of TAO in T. brucei, we genetically engineered T. brucei for conditional over-expression of the TAO gene. TAO over-expressing transgenic T. brucei was refractory to the development of the PCD-like phenomenon compared to the wild-type, indicating that expression of TAO might have a regulatory role on PCD development. Furthermore, the transgenic cells showed resistance to suramin and antrycide. We postulated that intracellular reactive oxygen species (ROS) may be involved in the mechanism of resistance to antrycide because augmentation of ROS in transgenic cells was lower than that in the wild-type cells following treatment with antrycide. These results suggest a possible correlation of PCD to drug resistance in T. brucei.
Предметные рубрики MeSH
AnimalsApoptosisDose-Response Relationship, DrugDrug ResistanceGene Expression Regulation, EnzymologicHumansIn Situ Nick-End LabelingMitochondrial ProteinsOxidoreductasesParasitic Sensitivity TestsPlant ProteinsQuinolinium CompoundsReactive Oxygen SpeciesSuraminTime FactorsTrypanocidal AgentsTrypanosoma brucei bruceiTrypanosomiasis, AfricanAlternative Oxidase