A program was established in 1984 to study several aspects of cell motility in developing systems. These systems now include 1) chemotaxis in Dictyostelium, 2) the migration of sea urchin primary mesenchyme cells, 3) the molecular basis of cell motility in vertebrate cells. and 4) growth cone and neuronal activity in Drosophila. A core facility has been established in the program which not only provides image processing and motion analysis technologies for participants, but which has evolved into a developmental facility for 2D and 3D dynamic image analyzing systems. The program also sponsors the Motility Seminar 6 times a semester in which invited speakers present seminars on current subjects of interest in cell motility and the cytoskeleton, and the Junior Motility Symposium which meets at least once each semester, in which graduate students and postdocs present formal seminars on their ongoing research. In the next program period, individual projects will investigate the following major questions: 1) how Dictyostelium amoebae behave in 3D in the natural chemotactic wave, and the defects exhibited by mutants selectively lacking sensory transduction and cytoskeletal molecules (Soll); 2) how a recently identified cell surface glycoprotein initiates migratory behavior in primary sea urchin mesenchyme cells and avian corneal fibroblasts (Solursh); 3) how the different tropomyosin isoforms and caldesmon regulate the interaction of actin and myosin in nonmuscle cell motility (Lin); and 4) how electric activity, intracellular Ca++, and protein kineses regulate Drosophila growth cone motility and neural growth, and the roles of adhesion molecules and ion channels (Wu). In addition, we will continue to develop new software packages for motion analysis in the core facility, continue the Motility Seminar and Junior Motility Symposium, and initiate a new yearly Senior Motility Symposium which will include outside speakers and project directors, and a biannual Core Facility Training and Demonstration Course for motion analysis technology. The core facility will also continue to serve all participants for microscopy, image processing and 2 and 3D motion analysis. This program project focuses on the central theme of cell motility and obtains its vitality from the intense interactions of the participants.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
5P01HD018577-11
Application #
2197677
Study Section
Maternal and Child Health Research Committee (HDMC)
Project Start
1984-04-01
Project End
1997-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
11
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Iowa
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Soll, David R; Wessels, Deborah; Kuhl, Spencer et al. (2009) How a cell crawls and the role of cortical myosin II. Eukaryot Cell 8:1381-96
Lusche, Daniel F; Wessels, Deborah; Soll, David R (2009) The effects of extracellular calcium on motility, pseudopod and uropod formation, chemotaxis, and the cortical localization of myosin II in Dictyostelium discoideum. Cell Motil Cytoskeleton 66:567-87
Wessels, Deborah; Kuhl, Spencer; Soll, David R (2009) 2D and 3D quantitative analysis of cell motility and cytoskeletal dynamics. Methods Mol Biol 586:315-35
Lin, Jim Jung-Ching; Li, Yan; Eppinga, Robbin D et al. (2009) Chapter 1: roles of caldesmon in cell motility and actin cytoskeleton remodeling. Int Rev Cell Mol Biol 274:1-68
Wessels, Deborah J; Kuhl, Spencer; Soll, David R (2009) Light microscopy to image and quantify cell movement. Methods Mol Biol 571:455-71
Ueda, Atsushi; Wu, Chun-Fang (2009) Effects of social isolation on neuromuscular excitability and aggressive behaviors in Drosophila: altered responses by Hk and gsts1, two mutations implicated in redox regulation. J Neurogenet 23:378-94
Ueda, Atsushi; Wu, Chun-Fang (2009) Role of rut adenylyl cyclase in the ensemble regulation of presynaptic terminal excitability: reduced synaptic strength and precision in a Drosophila memory mutant. J Neurogenet 23:185-99
Ueda, Atsushi; Wu, Chun-Fang (2008) Effects of hyperkinetic, a beta subunit of Shaker voltage-dependent K+ channels, on the oxidation state of presynaptic nerve terminals. J Neurogenet 22:1-13
Lee, J; Ueda, A; Wu, C-F (2008) Pre- and post-synaptic mechanisms of synaptic strength homeostasis revealed by slowpoke and shaker K+ channel mutations in Drosophila. Neuroscience 154:1283-96
Volk, A Paige Davis; Heise, Christine K; Hougen, Jami L et al. (2008) ClC-3 and IClswell are required for normal neutrophil chemotaxis and shape change. J Biol Chem 283:34315-26

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