Journal article
Drosophila Fascin is a novel downstream target of prostaglandin signaling during actin remodeling
Molecular biology of the cell, Vol.23(23), pp.4567-4578
12/2012
DOI: 10.1091/mbc.E12-05-0417
PMCID: PMC3510018
PMID: 23051736
Abstract
Although prostaglandins (PGs)-lipid signals produced downstream of cyclooxygenase (COX) enzymes-regulate actin cytoskeletal dynamics, their mechanisms of action are unknown. We previously established Drosophila oogenesis, in particular nurse cell dumping, as a new model to determine how PGs regulate actin remodeling. PGs, and thus the Drosophila COX-like enzyme Pxt, are required for both the parallel actin filament bundle formation and the cortical actin strengthening required for dumping. Here we provide the first link between Fascin (Drosophila Singed, Sn), an actin-bundling protein, and PGs. Loss of either pxt or fascin results in similar actin defects. Fascin interacts, both pharmacologically and genetically, with PGs, as reduced Fascin levels enhance the effects of COX inhibition and synergize with reduced Pxt levels to cause both parallel bundle and cortical actin defects. Conversely, overexpression of Fascin in the germline suppresses the effects of COX inhibition and genetic loss of Pxt. These data lead to the conclusion that PGs regulate Fascin to control actin remodeling. This novel interaction has implications beyond Drosophila, as both PGs and Fascin-1, in mammalian systems, contribute to cancer cell migration and invasion.
Details
- Title: Subtitle
- Drosophila Fascin is a novel downstream target of prostaglandin signaling during actin remodeling
- Creators
- Christopher M Groen - Anatomy and Cell Biology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USAAndrew J SpracklenTiffany N FaganTina L Tootle
- Resource Type
- Journal article
- Publication Details
- Molecular biology of the cell, Vol.23(23), pp.4567-4578
- DOI
- 10.1091/mbc.E12-05-0417
- PMID
- 23051736
- PMCID
- PMC3510018
- NLM abbreviation
- Mol Biol Cell
- ISSN
- 1059-1524
- eISSN
- 1939-4586
- Publisher
- American Society for Cell Biology; United States
- Grant note
- T32 GM067795 / NIGMS NIH HHS UL1 RR024979 / NCRR NIH HHS UL1RR024979 / NCRR NIH HHS T32GM067795 / NIGMS NIH HHS
- Language
- English
- Date published
- 12/2012
- Academic Unit
- Anatomy and Cell Biology
- Record Identifier
- 9984025356102771
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