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Published on: August 19, 2018
Increased association of dynamin II with myosin II in ras transformed NIH3T3 cells
Soon-Jeong Jeong1, Su-Gwan Kim, Jiyun Yoo
1Department of Oral Histology, College of Dentistry, Chosun University, Gwangju 501-759, South Korea.
Abstract:
Dynamin has been implicated in the formation of nascent vesicles through both endocytic and secretory pathways. However, dynamin has recently been implicated in altering the cell membrane shape during cell migration associated with cytoskeleton-related proteins. Myosin II has been implicated in maintaining cell morphology and in cellular movement. Therefore, reciprocal immunoprecipitation was carried out to identify the potential relationship between dynamin II and myosin II. The dynamin II expression level was higher when co-expressed with myosin II in Ras transformed NIH3T3 cells than in normal NIH3T3 cells. Confocal microscopy also confirmed the interaction between these two proteins. Interestingly, exposing the NIH3T3 cells to platelet-derived growth factor altered the interaction and localization of these two proteins. The platelet-derived growth factor treatment induced lamellipodia and cell migration, and dynamin II interacted with myosin II. Grb2, a 24 kDa adaptor protein and an essential element of the Ras signaling pathway, was found to be associated with dynamin II and myosin II gene expression in the Ras transformed NIH3T3 cells. These results suggest that dynamin II acts as an intermediate messenger in the Ras signal transduction pathway leading to membrane ruffling and cell migration.
Insights
Dynamin II and myosin II interact and influence cell migration. This interaction is modulated by platelet-derived growth factor and involves the Ras signaling pathway, suggesting dynamin II
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- Dynamin is involved in vesicle formation via endocytic and secretory pathways.
- Dynamin also influences cell membrane shape during cell migration, interacting with cytoskeleton proteins.
- Myosin II is crucial for maintaining cell morphology and driving cellular movement.
Purpose of the Study:
- To investigate the potential relationship between dynamin II and myosin II.
- To explore the role of dynamin II and myosin II in cell migration signaling.
Main Methods:
- Reciprocal immunoprecipitation to detect protein interactions.
- Confocal microscopy to visualize protein localization.
- Co-expression studies in NIH3T3 cells (normal and Ras-transformed).
- Treatment with platelet-derived growth factor (PDGF).
Main Results:
- Dynamin II and myosin II were found to interact.
- Dynamin II expression was elevated when co-expressed with myosin II in Ras-transformed cells.
- Platelet-derived growth factor treatment altered dynamin II and myosin II interaction and localization, inducing lamellipodia and cell migration.
- Grb2 adaptor protein associated with dynamin II and myosin II gene expression in Ras-transformed cells.
Conclusions:
- Dynamin II and myosin II interact and are involved in PDGF-induced cell migration.
- Dynamin II may act as an intermediate messenger in the Ras signal transduction pathway.
- The dynamin II-myosin II complex influences membrane ruffling and cell migration.
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