Leishmaniasis, a neglected tropical disease, is caused by the intracellular protozoan parasite . Upon its transmission through a sandfly bite, binds and enters host phagocytic cells, ultimately resulting in a cutaneous or visceral form of the disease. The limited therapeutics available for leishmaniasis, in combination with this parasite's techniques to evade the host immune system, call for exploring various methods to target this infection. To this end, our laboratory has been characterizing how is internalized by phagocytic cells through the activation of multiple host cell signaling pathways. This protocol, which we use routinely for our experiments, delineates how to infect mammalian macrophages with either promastigote or amastigote forms of the parasite. Subsequently, the number of intracellular parasites, external parasites, and macrophages can be quantified using immunofluorescence microscopy and semi-automated analysis protocols. Studying the pathways that underlie uptake by phagocytes will not only improve our understanding of these host-pathogen interactions but may also provide a foundation for discovering additional treatments for leishmaniasis. Key features • This protocol visualizes and quantifies multiple intracellular forms of . • It offers flexibility at various points for researchers to introduce modifications according to their study needs.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11166538 | PMC |
http://dx.doi.org/10.21769/BioProtoc.5009 | DOI Listing |
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