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Cell cycle-dependent morphological changes in the actin cytoskeleton induced by agents which elevate cyclic AMP
C J McNamee1, S R Pennington, P Sheterline
1Department of Human Anatomy and Cell Biology, University of Liverpool, UK.
Cell Biology International
|September 1, 1995
Summary
Agents increasing cyclic adenosine-5'-monophosphate levels cause Swiss 3T3 fibroblasts to develop arborised morphology by reorganizing actin filaments. This response is cell cycle-dependent, primarily occurring in the G1 phase.
Area of Science:
- Cell Biology
- Biochemistry
- Cytoskeleton Dynamics
Background:
- Cyclic adenosine-5'-monophosphate (cAMP) is a crucial second messenger involved in various cellular processes.
- Fibroblast morphology and actin cytoskeleton organization are critical for cell function and response to stimuli.
Purpose of the Study:
- To investigate the morphological and cytoskeletal changes in Swiss 3T3 fibroblasts induced by agents that increase intracellular cAMP.
- To determine the cell cycle dependency of the cAMP-mediated arborisation response.
Main Methods:
- Treatment of sub-confluent Swiss 3T3 fibroblasts with agents that elevate intracellular cAMP.
- Analysis of actin filament organization using fluorescence microscopy.
- Assessment of cell cycle phase distribution and response timing after serum readdition.
Main Results:
- Agents increasing cAMP induced a highly arborised morphology in a proportion of fibroblasts.
- Actin filaments reorganized from stress fibers to a network within arborisations without changes in overall polymerization.
- The arborisation response was restricted to approximately 30% of cells in asynchronous cultures and occurred primarily in the G1 phase of the cell cycle.
Conclusions:
- Increased intracellular cAMP triggers significant actin cytoskeleton reorganization leading to fibroblast arborisation.
- The arborisation response is tightly regulated by the cell cycle, specifically occurring during the G1 phase.
- These findings highlight the role of cAMP signaling in modulating cell shape and cytoskeletal dynamics in a cell cycle-dependent manner.