A program was established in 1984 to study the regulation of cell motility in developing systems. The basic research projects supported by the program now include 1) cell motility, chemotaxis and the role of the cytoskeleton in Dictyostelium, 2) the role of caldesmon and the tropomyosins in vertebrate cell motility, and 3) the role of regulatory cascades in growth cone motility during neuronal development and modification. A core Facility was originally established which provides computer-assisted image processing and motion analysis systems for use by participants. The Core Facility has evolved into a technology development facility as well as a service facility for the development of advanced 2D and 3D motion analysis systems. The program also sponsors the Cell Motility Seminar Series, in which outside speakers present seminars on topic of interest to the Program, a Junior Symposium, in which graduate students and post-docs present seminars, and the Annual Motility Symposium, a half day formal symposium including senior scientists from the University of Iowa and other universities. The program has stimulated collaborations between program participants which in all cases have led to joint publications, and a number of new projects related to the developmental biology of cell motility. In the next program project, individual projects will include the following: 1) chemotaxis and the involvement of select cytoskeletal elements relying primarily on 3D dynamic image analysis systems recently developed in the Core Facility (Soll lab); 2) the roles of caldesmon, tropomyosin and the myosins in intracellular and cellular motility, and cytokinesis in animal cells (Lin lab); 3) the role of regulatory cascades and the cytoskeleton in neuronal development and plasticity (Wu lab); and 4) development of an advanced 3D dynamic image analysis system and """"""""direct image"""""""" reconstruction software (Voss, Core Facility). In addition, the Core Facility will function as a service facility, and the Cell Motility Seminar Series, the Junior Symposium and the Annual Motility Symposium will be continued. This program project focuses on the general them of cell motility in development, and continues to obtain vitality from the constant 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 #
5P01HD018577-15
Application #
2673495
Study Section
Pediatrics Subcommittee (CHHD)
Project Start
1984-04-01
Project End
2002-03-31
Budget Start
1998-04-01
Budget End
1999-03-31
Support Year
15
Fiscal Year
1998
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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