Exocytotic release of hormones and neurotransmitters is central to intercellular communication and synaptic transmission. The process is fundamental to the normal function of the endocrine, cardiovascular and nervous systems. In the previous grant period we made fundamental advances in defining the steps involved in the pathway of Ca2+-activated exocytosis using intact and digitonin permeabilized bovine chromaffin cells. An important part of the competing renewal is the extension of the investigations by implementation of two new systems that we have developed for studying secretion. They allow us to manipulate more directly than heretofore possible components of the secretory pathway. We have developed a novel transient transfection system in bovine chromaffin cells (primary, non-dividing cells) to study the role of specific proteins in the secretory pathway. A key part of the approach is to coexpress with a protein of interest, human growth hormone (GH), which serves as a reporter for the regulated secretory pathway in the small fraction of cells that are transfected. We also found that chromaffin granule membranes injected into frog oocytes undergo exocytosis. This reconstitution technique allows us for the first time to manipulate the secretory vesicle apart from the cell to explore components of the secretory vesicle necessary for exocytosis. These new systems will allows us to ask more precise questions concerning the biochemical mechanisms underlying the pathway. The development of both these systems allows us to use functional assays to study chromaffin granule as well as other cellular protein components in exocytosis. The following topics will be investigated: 1) The role of the GTP-binding protein rab3a in regulated exocytosis in adrenal chromaffin cells. 2) The role in exocytosis of synaptotagmin (p65), an integral membrane protein of secretory vesicles. 3) The role of polyphosphoinositides (PPIs) in exocytosis. 4) The identification of protein components on the chromaffin granule membrane important in the exocytotic response in frog oocytes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK027959-12A2
Application #
2138074
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1981-01-01
Project End
1998-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
12
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Pharmacology
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Krasnoperov, Valery; Bittner, Mary A; Mo, Wenjun et al. (2002) Protein-tyrosine phosphatase-sigma is a novel member of the functional family of alpha-latrotoxin receptors. J Biol Chem 277:35887-95
Sun, Lei; Bittner, Mary A; Holz, Ronald W (2002) Rim and exocytosis: Rab3a-binding and secretion-enhancing domains are separate and function independently. Ann N Y Acad Sci 971:244-7
Johns, L M; Levitan, E S; Shelden, E A et al. (2001) Restriction of secretory granule motion near the plasma membrane of chromaffin cells. J Cell Biol 153:177-90
Sun, L; Bittner, M A; Holz, R W (2001) Rab3a binding and secretion-enhancing domains in Rim1 are separate and unique. Studies in adrenal chromaffin cells. J Biol Chem 276:12911-7
Micheva, K D; Holz, R W; Smith, S J (2001) Regulation of presynaptic phosphatidylinositol 4,5-biphosphate by neuronal activity. J Cell Biol 154:355-68
Hlubek, M D; Stuenkel, E L; Krasnoperov, V G et al. (2000) Calcium-independent receptor for alpha-latrotoxin and neurexin 1alpha [corrected] facilitate toxin-induced channel formation: evidence that channel formation results from tethering of toxin to membrane. Mol Pharmacol 57:519-28
Bittner, M A (2000) Alpha-latrotoxin and its receptors CIRL (latrophilin) and neurexin 1 alpha mediate effects on secretion through multiple mechanisms. Biochimie 82:447-52
Bittner, M A; Holz, R W (2000) Latrotoxin stimulates secretion in permeabilized cells by regulating an intracellular Ca2+ - and ATP-dependent event: a role for protein kinase C. J Biol Chem 275:25351-7
Krasnoperov, V; Bittner, M A; Holz, R W et al. (1999) Structural requirements for alpha-latrotoxin binding and alpha-latrotoxin-stimulated secretion. A study with calcium-independent receptor of alpha-latrotoxin (CIRL) deletion mutants. J Biol Chem 274:3590-6
Ichtchenko, K; Bittner, M A; Krasnoperov, V et al. (1999) A novel ubiquitously expressed alpha-latrotoxin receptor is a member of the CIRL family of G-protein-coupled receptors. J Biol Chem 274:5491-8

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