Tanmay Lele
Ph.D., 2002, Purdue University
Assistant Professor
Ph : 352-392-0317
tlele@che.ufl.edu
329 Chemical Engineering Building
Faculty Web Page
Areas
Cell mechano-transduction
Cytoskeletal force generation
Nano-biotechnology
 
Cell mechano-transduction
Hydrodynamic shear due to blood flow or deformation of tissue exerts forces on cells. Cells transduce these forces into an intracellular response through a process called mechano-transduction. The molecular level mechanisms of mechano-transduction are poorly understood. We develop and apply new engineering technologies for mechanical manipulation and simultaneous visualization of molecular processes inside living cells. This research has applications in understanding diseases of mechano-transduction, such as atherosclerosis and myopathies.
 
Cytoskeletal force generation
The cytoskeleton inside cells is a protein-based polymeric network that generates mechanical pushing and pulling forces. Forces generated in the cytoskeleton allow cells to spread, move and divide. We study the molecular mechanisms of force generation in the microtubule and acto-myosin cytoskeleton. We use a combination of imaging techniques including femtosecond laser ablation and fluorescence photo-bleaching along with computational modeling.
Research Research Research Research
Microtubules Intermediate Filaments Centrosome (green) with nucleus(blue) Actin(green) with (red) and necleus(blue)
 
Nano-biotechnology
To improve the performance of current biomedical implants, it is necessary to achieve control over the fate of cells that interact with the implants. We are developing novel strategies of modulating the surface of devices using nano-structured coatings. The nanostructures modulate cells by influencing molecular-level processes during cell-surface adhesion. We also study the molecular mechanisms by which cell adhesion is modulated by nano-structures.

Research

SEM micrographs of cells on nanorods. Cells are unable
to spread on nanorods. White arrows are filopodia-like
structures. Scale bar of (A) is 3 µm &1 µm(inset).
Scale bar of (B) is 5 µm & 2 µm (inset).
 
Recent Publications
1. Wu, J., Lee, K.C., Dickinson, R.B., and Lele, T.P., How dynein and microtubules rotate the nucleus. J Cell Physiol, 2011. In press.
2. Russell, R.J., Grubbs, A.Y., Mangroo, S.P., Nakasone, S.E., Dickinson, R.B., and Lele, T.P., Sarcomere length fluctuations and flow in capillary endothelial cells. Cytoskeleton, 2011. In press.
3 Lee, J., Wang, Y.L., Ren, F., and Lele, T.P., Stamp Wound Assay for Studying Coupled Cell Migration and Cell Debris Clearance. Langmuir, 2010. 26(22): p. 16672-16676.
4. Chancellor, T.J., Lee, J., Thodeti, C.K., and Lele, T., Actomyosin tension exerted on the nucleus through nesprin-1 connections influences endothelial cell adhesion, migration, and cyclic strain-induced reorientation. Biophys J, 2010. 99(1): p. 115-123.
5. Russell, R.J., Xia, S.L., Dickinson, R.B., and Lele, T.P., Sarcomere mechanics in capillary endothelial cells. Biophys J, 2009. 97(6): p. 1578-1585.