Recent studies from our laboratory uncovered a novel mechanism for cell invasion by the protozoan Trypanosoma cruzi. Prior to entry into non- phagocytic mammalian cells, host lysosomes are recruited to the parasite attachment site and gradually fuse with the plasma membrane, originating the parasite-containing vacuole. In our search for signal transduction events involved in this process, we found that infective trypomastigotes mobilize Ca2 plus from host cell intracellular stores, inducing transient increases in the cytosolic free Ca2 plus concentration of a variety of mammalian cell types. Rapid rearrangements in the host cell cortical actin cytoskeleton, a condition known to result in enhanced T. cruzi invasion, are observed as a consequence of trypomastigote-induced Ca2 plus-transients. Prevention of these transients significantly inhibits host cell invasion by the parasites. We now plan to directly investigate the link between the T. cruzi-induced intracellular free Ca2 plus transients and the mobilization and fusion of lysosomes with the plasma membrane in mammalian cells. Specifically, we will: 1) using a video-microscopy assay, examine the role of host cell cytosolic free Ca2 plus transients on the recruitment and/or plasma membrane fusion of lysosomes induced by T. cruzi; 2) investigate the role of the major PKC substrate, Ca2 plus-calmodulin and actin-binding protein MARCKS in the host cell events leading to lysosome fusion and T. cruzi invasion; 3) use a permeabilized mammalian cell system to investigate the molecular mechanisms involved in Ca2 plus-regulated lysosome exocytosis, specifically the role of the NSF/SNAP/SNARE fusion complex, synaptotagmin, annexins and monomeric and trimeric GTP-binding proteins; 4) correlate the data obtained in the lysosome exocytosis assay with T. cruzi invasion, using specific inhibitors and cellular microinjection. These studies will advance our knowledge of the unusual cell invasion mechanism utilized by the important human pathogen T. cruzi, as well as of fundamental membrane traffic events involving lysosomes in mammalian cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI034867-07
Application #
6137182
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Program Officer
Fairfield, Alexandra
Project Start
1994-01-01
Project End
2002-12-31
Budget Start
2000-01-01
Budget End
2000-12-31
Support Year
7
Fiscal Year
2000
Total Cost
$234,606
Indirect Cost
Name
Yale University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Mittra, Bidyottam; Cortez, Mauro; Haydock, Andrew et al. (2013) Iron uptake controls the generation of Leishmania infective forms through regulation of ROS levels. J Exp Med 210:401-16
Mittra, Bidyottam; Andrews, Norma W (2013) IRONy OF FATE: role of iron-mediated ROS in Leishmania differentiation. Trends Parasitol 29:489-96
Fernandes, Maria CecĂ­lia; Andrade, Leonardo Rodrigues de; Andrews, Norma Windsor et al. (2011) Trypanosoma cruzi trypomastigotes induce cytoskeleton modifications during HeLa cell invasion. Mem Inst Oswaldo Cruz 106:1014-6
Albertti, L A G; Macedo, A M; Chiari, E et al. (2010) Role of host lysosomal associated membrane protein (LAMP) in Trypanosoma cruzi invasion and intracellular development. Microbes Infect 12:784-9
da Silva, Claudio V; Kawashita, Silvia Y; Probst, Christian M et al. (2009) Characterization of a 21kDa protein from Trypanosoma cruzi associated with mammalian cell invasion. Microbes Infect 11:563-70
Chakrabarti, Sabyasachi; Andrade, Luciana O; Andrews, Norma W (2005) Trypanosoma cruzi invades synaptotagmin VII-deficient cells by a PI-3 kinase independent pathway. Mol Biochem Parasitol 141:125-8
Andrade, Luciana O; Andrews, Norma W (2004) Lysosomal fusion is essential for the retention of Trypanosoma cruzi inside host cells. J Exp Med 200:1135-43
Jaiswal, Jyoti K; Chakrabarti, Sabyasachi; Andrews, Norma W et al. (2004) Synaptotagmin VII restricts fusion pore expansion during lysosomal exocytosis. PLoS Biol 2:E233
Roy, Deepannita; Liston, David R; Idone, Vincent J et al. (2004) A process for controlling intracellular bacterial infections induced by membrane injury. Science 304:1515-8
Huynh, Chau; Andrews, Norma W (2003) Leishmania amazonensis Rab7 promotes toxicity of the amino acid ester Leu-OMe in amastigote megasomes. Mol Biochem Parasitol 132:101-4

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