کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3416434 1593701 2015 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Simultaneous multi-parametric analysis of Leishmania and of its hosting mammal cells: A high content imaging-based method enabling sound drug discovery process
ترجمه فارسی عنوان
تجزیه و تحلیل چند پارامتری همزمان لیشمانیا و سلولهای میزبان آن: یک روش مبتنی بر تصویربرداری با محتوای بالا که قادر به فرآیند کشف دارو می باشد
کلمات کلیدی
لیشمانیا، غربالگری مواد مخدر، تصویربرداری میکروسکوپ
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی میکروب شناسی
چکیده انگلیسی


• Microscopy imaging of Leishmania–host cell interactions.
• High content microscopy analysis.
• Low to high throughput microscopy analysis.
• Intravital microscopy imaging in drug discovery.

Leishmaniasis is a vector-borne disease for which only limited therapeutic options are available. The disease is ranked among the six most important tropical infectious diseases and represents the second-largest parasitic killer in the world. The development of new therapies has been hampered by the lack of technologies and methodologies that can be integrated into the complex physiological environment of a cell or organism and adapted to suitable in vitro and in vivo Leishmania models. Recent advances in microscopy imaging offer the possibility to assess the efficacy of potential drug candidates against Leishmania within host cells. This technology allows the simultaneous visualization of relevant phenotypes in parasite and host cells and the quantification of a variety of cellular events. In this review, we present the powerful cellular imaging methodologies that have been developed for drug screening in a biologically relevant context, addressing both high-content and high-throughput needs. Furthermore, we discuss the potential of intra-vital microscopy imaging in the context of the anti-leishmanial drug discovery process.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Microbial Pathogenesis - Volume 88, November 2015, Pages 103–108
نویسندگان
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