It is now aparent that regulated exocytosis is not restricted to specialized secretory cells, and that conventional lysosomes can respond to elevations in intracellular free Ca2+ by fusing with the plasma membrane. Investigating the physiological function of this ubiquitous lysosomal exocytic pathway, we found that it plays a central role in the mechanism by which mammalian cells reseal their plasma membrane after injury. Our previous studies also implicated synaptotagmin VII (Syt VII), a widely expressed member of the synaptotagmin family of putative Ca2+ sensors, in the regulation of lysosomal exocytosis and plasma membrane resealing. We now plan to expand our studies of the physiological role of Ca2+-regulated lysosomal exocytosis, and to characterize unique molecular interactions and dynamic propel-ties involved in this process.
Our specific aims are: 1) To examine the resealing capacity of primary skin fibroblasts with genetic defects affecting lysosomes, using a collagen matrix contraction model of plasma membrane wounding and repair. Completion of this aim will allow us to determine if defects in plasma membrane resealing are a component of the serious symptoms associated with a series of lysosome-related genetic syndromes. 2) To investigate the role of the unconventional SNARE VAMP7 and of the synaptotagmin isoform Syt VII in the regulation of lysosomal exocytosis and plasma membrane repair. These studies will determine if Syt VII plays an essential role in the formation of specific SNARE complexes involved in lysosomal exocytosis, and will clarify the function of the lysosomal SNARE TIVAMP/VAMP-7, previously implicated in exocytic events associated with neurite outgrowth. 3) To verify if molecular interactions that regulate Ca2+-dependent exocytosis of conventional lysosomes also control secretion of the lysosome-related secretory granules of cytotoxic T lymphocytes (CTLs) and mast cells. These studies will provide important new information on the mechanisms regulating the exocytosis of lysosome-related granules that play critical roles in the immune response. 4) To investigate the spatial-temporal dynamics of Ca2+-regulated lysosomal exocytosis by total internal reflection fluorescence microscopy (TIR-FM). This powerful imaging technique will allow us to obtain quantitative parameters on the motion and distribution of lysosomes near the plasma membrane, map fusion sites on individual cells, and determine the diffusion coefficient of lysosomal membrane proteins after fusion. Taken together, the information generated by this project will significantly improve our understanding of fundamental biological processes involving regulated exocytosis of lysosomes, including maintenance of plasma membrane integrity and degranulation in cells of the immune system.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM064625-01A1
Application #
6545189
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Shapiro, Bert I
Project Start
2002-08-01
Project End
2006-07-31
Budget Start
2002-08-01
Budget End
2003-07-31
Support Year
1
Fiscal Year
2002
Total Cost
$349,313
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
Castro-Gomes, Thiago; Corrotte, Matthias; Tam, Christina et al. (2016) Plasma Membrane Repair Is Regulated Extracellularly by Proteases Released from Lysosomes. PLoS One 11:e0152583
Corrotte, M; Castro-Gomes, T; Koushik, A B et al. (2015) Approaches for plasma membrane wounding and assessment of lysosome-mediated repair responses. Methods Cell Biol 126:139-58
Miller, Heather; Castro-Gomes, Thiago; Corrotte, Matthias et al. (2015) Lipid raft-dependent plasma membrane repair interferes with the activation of B lymphocytes. J Cell Biol 211:1193-205
Fernandes, Maria Cecilia; Corrotte, Matthias; Miguel, Danilo C et al. (2015) The exocyst is required for trypanosome invasion and the repair of mechanical plasma membrane wounds. J Cell Sci 128:27-32
Andrews, N W; Corrotte, M; Castro-Gomes, T (2015) Above the fray: Surface remodeling by secreted lysosomal enzymes leads to endocytosis-mediated plasma membrane repair. Semin Cell Dev Biol 45:10-7
Andrews, N W; Perez, F (2015) The plasma membrane repair shop: Fixing the damage. Semin Cell Dev Biol 45:1
Castro-Gomes, T; Koushik, A B; Andrews, N W (2014) ESCRT: nipping the wound in the bud? Trends Biochem Sci 39:307-9
Andrews, Norma W; Almeida, Patricia E; Corrotte, Matthias (2014) Damage control: cellular mechanisms of plasma membrane repair. Trends Cell Biol 24:734-42
Hissa, Barbara; Pontes, Bruno; Roma, Paula Magda S et al. (2013) Membrane cholesterol removal changes mechanical properties of cells and induces secretion of a specific pool of lysosomes. PLoS One 8:e82988
Flannery, Andrew R; Renberg, Rebecca L; Andrews, Norma W (2013) Pathways of iron acquisition and utilization in Leishmania. Curr Opin Microbiol 16:716-21

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