The research outlined in this proposal deals with the broad topics of synthesis and transport of lipid molecules within mammalian cells, and is important for a proper understanding of membrane biogenesis. The following areas will be investigated. We will continue our studies with fluorescent lipid analogues which permit traditional lipid biochemical analyses to be performed and correlated with information about the intracellular location of lipid metabolites determined by fluorescence microscopy in living cells. The general applicability of this approach will be examined in parallel studies using isotopically labeled lipids and EM autoradiography. We will study the internalization and degradation of both radiolabeled lipids and fluorescent lipid analogues after insertion into the plasma membrane of cells by lipid transfer from liposomes. These data will be compared to the rate of appearance of newly synthesized lipids at the cell surface to determine if recycling of plasma membrane lipids occurs. We will study the behavior of fluorescent lipids, liposomes, and other agents after microinjection into single cells. These experiments are designed to develop an in situ approach for studying the compartmentalization of lipids during their biosynthesis and for probing mechanisms of lipid transport within individual cells. Finally, using a selection procedure based on fluorescence photobleaching, we will attemtp to isolate mutant cells which are defective in their ability to incorporate, metabolize, and/or translocate the fluorescent lipid analogues among intracellular membranes. The studies listed above are basic to an understanding of membrane assembly in eukaryotes, and are fundamental to the development of rational treatments of membrane or cell surface-related disease states.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM022942-13
Application #
3271422
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1979-03-01
Project End
1989-02-28
Budget Start
1988-03-01
Budget End
1989-02-28
Support Year
13
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Carnegie Institution of Washington, D.C.
Department
Type
DUNS #
072641707
City
Washington
State
DC
Country
United States
Zip Code
20005
Ohmine, Seiga; Singh, Raman Deep; Marks, David L et al. (2013) Viral attachment induces rapid recruitment of an innate immune sensor (TRIM5?) to the plasma membrane. J Innate Immun 5:414-24
Singh, Raman Deep; Schroeder, Andreas S; Scheffer, Luana et al. (2013) Prominin-2 expression increases protrusions, decreases caveolae and inhibits Cdc42 dependent fluid phase endocytosis. Biochem Biophys Res Commun 434:466-72
Marks, David L; Holicky, Eileen L; Wheatley, Christine L et al. (2012) Role of protein kinase d in Golgi exit and lysosomal targeting of the transmembrane protein, Mcoln1. Traffic 13:565-75
Wang, Shaohua; Singh, Raman Deep; Godin, Lindsay et al. (2011) Endocytic response of type I alveolar epithelial cells to hypertonic stress. Am J Physiol Lung Cell Mol Physiol 300:L560-8
Penheiter, Sumedha G; Singh, Raman Deep; Repellin, Claire E et al. (2010) Type II transforming growth factor-beta receptor recycling is dependent upon the clathrin adaptor protein Dab2. Mol Biol Cell 21:4009-19
Singh, Raman Deep; Marks, David L; Holicky, Eileen L et al. (2010) Gangliosides and beta1-integrin are required for caveolae and membrane domains. Traffic 11:348-60
Watzlawik, J; Holicky, E; Edberg, D D et al. (2010) Human remyelination promoting antibody inhibits apoptotic signaling and differentiation through Lyn kinase in primary rat oligodendrocytes. Glia 58:1782-93
Bachar, Adi R; Scheffer, Lea; Schroeder, Andreas S et al. (2010) Humanin is expressed in human vascular walls and has a cytoprotective effect against oxidized LDL-induced oxidative stress. Cardiovasc Res 88:360-6
Cheng, Zhi-Jie; Singh, Raman Deep; Holicky, Eileen L et al. (2010) Co-regulation of caveolar and Cdc42-dependent fluid phase endocytosis by phosphocaveolin-1. J Biol Chem 285:15119-25
Cheng, Zhi-Jie; Singh, Raman Deep; Wang, Teng-Ke et al. (2010) Stimulation of GLUT4 (glucose transporter isoform 4) storage vesicle formation by sphingolipid depletion. Biochem J 427:143-50

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