?Project(1((Goldman) In this project, we are testing the hypothesis that the assembly states and mechanical properties of the type III intermediate filament network composed of vimentin is an important component of the cytoskeleton in regulating the micromechanical properties of cells in response to mechanical stress and in signal transduction and cell motility. Vimentin is the major intermediate filament protein expressed in mesenchymal cells and is critically important for cell migration, wound healing, the epithelial-mesenchymal-transition in normal development and in cancer, and in the response of cells to mechanical stress. We propose to use several microscopy methods including 3D-structured illumination, total internal reflection, and cryo-electron tomography to investigate the structure of vimentin in cells. We will use a wound healing model to identify steps in the process of vimentin network assembly/disassembly in the response of fibroblasts to mechanical stress, including the regulation of vimentin synthesis. These studies will also include the identification and characterization of interactions among vimentin, microtubules, and actin stress fibers, as well as the details of the interactions of vimentin with focal adhesions. The effects of different vimentin network assembly states on whole cell and subcellular mechanical properties will also be examined by micro-rheological methods and atomic force microscopy. Finally, the role of vimentin phosphorylation on network assembly, wound healing, interactions with other cytoskeletal components and cellular structures, and cellular mechanics will also be examined using both whole cell and biochemical approaches.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
2P01GM096971-06A1
Application #
9491497
Study Section
Special Emphasis Panel (ZRG1)
Project Start
Project End
Budget Start
2018-09-01
Budget End
2019-03-31
Support Year
6
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Type
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Wu, Pei-Hsun; Aroush, Dikla Raz-Ben; Asnacios, Atef et al. (2018) A comparison of methods to assess cell mechanical properties. Nat Methods 15:491-498
Robert, Amélie; Tian, Peirun; Adam, Stephen A et al. (2018) Kinesin-dependent transport of keratin filaments: a unified mechanism for intermediate filament transport. FASEB J :fj201800604R
Li, Wen; Zhang, Liyuan; Ge, Xuehui et al. (2018) Microfluidic fabrication of microparticles for biomedical applications. Chem Soc Rev 47:5646-5683
Wang, Zheng; Divanyan, Alex; Jourd'heuil, Frances L et al. (2018) Vimentin expression is required for the development of EMT-related renal fibrosis following unilateral ureteral obstruction in mice. Am J Physiol Renal Physiol 315:F769-F780
Wang, Liqun; Xia, Jing; Li, Jonathan et al. (2018) Tissue and cellular rigidity and mechanosensitive signaling activation in Alexander disease. Nat Commun 9:1899
Bucki, Robert; Durna?, Bonita; W?tek, Marzena et al. (2018) Targeting polyelectrolyte networks in purulent body fluids to modulate bactericidal properties of some antibiotics. Infect Drug Resist 11:77-86
Prakadan, Sanjay M; Shalek, Alex K; Weitz, David A (2017) Scaling by shrinking: empowering single-cell 'omics' with microfluidic devices. Nat Rev Genet 18:345-361
Costigliola, Nancy; Ding, Liya; Burckhardt, Christoph J et al. (2017) Vimentin fibers orient traction stress. Proc Natl Acad Sci U S A 114:5195-5200
Zaritsky, Assaf; Obolski, Uri; Gan, Zhuo et al. (2017) Decoupling global biases and local interactions between cell biological variables. Elife 6:
Roudot, Philippe; Liya Ding; Jaqaman, Khuloud et al. (2017) Piecewise-Stationary Motion Modeling and Iterative Smoothing to Track Heterogeneous Particle Motions in Dense Environments. IEEE Trans Image Process 26:5395-5410

Showing the most recent 10 out of 53 publications