Alveolar macrophages play a major role in pulmonary homeostasis by clearing injurious agents from the lung. Macrophages removes these agents by internalizing them and directing them to lysosomes where they are sequestered and degraded. Derangement's in vesicle traffic or lysosome functions result in a compromise of normal lung function. It is proposed to examine the mechanisms involved in intracellular vesicle traffic and lysosome function. The investigators demonstrated extensive lysosome-lysosome-fusion using both in vivo and in vitro assays. They demonstrated that a heterotrimeric G-protein, tentatively identified as a G-alpha-i is required from homotypic lysosome fusion. They now propose to determine the role of this G-protein plays in both the specificity and mechanism of lysosome fusion. In addition they will determine the factors that allow an endosome to gain the ability to fuse with lysosomes. This will be accomplished by examining the properties of endosomes that do or do not show fusion with lysosome. These endosomes are obtained using a unique procedure that synchronizes endosome formation and movement. The investigators have cloned the gene responsible of the beige/Chediak-Higashi Syndrome. This autosomal recessive diseases results in a phenotype which affects lysosomes, cytolytic granules, melanosomes, and platelet dense granules. Antisera against the Beige/Chediak protein will be used to probe the function of the gene product and its subcellular location. They developed procedures to measure lysosome size. Using these procedures and in vitro fusion assay they will determine whether the CHS/beige protein affects fusion or fission. These assays will also be used to define the biochemical function of this protein. The investigators have also identified a gene, VPS 41, in yeast that affects vacuole biogenesis, mutations give rise to many small vacuoles. They cloned this gene and its human and plant homologues. The yeast protein is involved in transfer of lysosomal enzymes from the Golgi to the late endosome. Antibodies prepared to the yeast or human gene will be used to defines its location and function. These studies will yield insight into the mechanisms of lysosome biogenesis and the molecules that regulate endocytic traffic and vesicle size.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37HL026922-21
Application #
6388879
Study Section
Lung Biology and Pathology Study Section (LBPA)
Program Officer
Musson, Robert
Project Start
1981-05-01
Project End
2002-08-31
Budget Start
2001-09-01
Budget End
2002-08-31
Support Year
21
Fiscal Year
2001
Total Cost
$308,033
Indirect Cost
Name
University of Utah
Department
Pathology
Type
Schools of Medicine
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
White, Carine; Yuan, Xiaojing; Schmidt, Paul J et al. (2013) HRG1 is essential for heme transport from the phagolysosome of macrophages during erythrophagocytosis. Cell Metab 17:261-70
Bagley, Dustin C; Paradkar, Prasad N; Kaplan, Jerry et al. (2012) Mon1a protein acts in trafficking through the secretory apparatus. J Biol Chem 287:25577-88
Durchfort, Nina; Verhoef, Shane; Vaughn, Michael B et al. (2012) The enlarged lysosomes in beige j cells result from decreased lysosome fission and not increased lysosome fusion. Traffic 13:108-19
Wilson, Jude; Huynh, Chau; Kennedy, Kathleen A et al. (2008) Control of parasitophorous vacuole expansion by LYST/Beige restricts the intracellular growth of Leishmania amazonensis. PLoS Pathog 4:e1000179
Kaplan, Jerry; De Domenico, Ivana; Ward, Diane McVey (2008) Chediak-Higashi syndrome. Curr Opin Hematol 15:22-9
Paradkar, Prasad N; De Domenico, Ivana; Durchfort, Nina et al. (2008) Iron depletion limits intracellular bacterial growth in macrophages. Blood 112:866-74
Kieffer, Collin; Skalicky, Jack J; Morita, Eiji et al. (2008) Two distinct modes of ESCRT-III recognition are required for VPS4 functions in lysosomal protein targeting and HIV-1 budding. Dev Cell 15:62-73
De Domenico, Ivana; Ward, Diane McVey; Langelier, Charles et al. (2007) The molecular mechanism of hepcidin-mediated ferroportin down-regulation. Mol Biol Cell 18:2569-78
Ward, Diane McVey; Vaughn, Michael B; Shiflett, Shelly L et al. (2005) The role of LIP5 and CHMP5 in multivesicular body formation and HIV-1 budding in mammalian cells. J Biol Chem 280:10548-55
Huynh, Chau; Roth, Doris; Ward, Diane M et al. (2004) Defective lysosomal exocytosis and plasma membrane repair in Chediak-Higashi/beige cells. Proc Natl Acad Sci U S A 101:16795-800

Showing the most recent 10 out of 35 publications