Na, SungsooWan, QiaoqiaoLi, JiliangYokota, Hiroki2013-09-052013-09-052013-09-05https://hdl.handle.net/1805/3520http://dx.doi.org/10.7912/C2/1335Indiana University-Purdue University Indianapolis (IUPUI)Mechanical force environment is a major factor that influences cellular homeostasis and remodeling. The prevailing wisdom in this field demonstrated that a threshold of mechanical forces or deformation was required to affect cell signaling. However, by using a fluorescence resonance energy transfer (FRET)-based approach, we found that C28/I2 chondrocytes exhibited an increase in RhoA activities in response to high shear stress (10 or 20 dyn/cm2), while they showed a decrease in their RhoA activities to intermediate shear stress at 5 dyn/cm2. No changes were observed under low shear stress (2 dyn/ cm2). The observed two-level switch of RhoA activities was closely linked to the shear stress-induced alterations in actin cytoskeleton and traction forces. In the presence of constitutively active RhoA (RhoA-V14), intermediate shear stress suppressed RhoA activities, while high shear stress failed to activate them. Collectively, these results herein suggest that intensities of shear stress are critical in differential activation and inhibition of RhoA activities in chondrocytes.en-USBiomedical EngineeringBiomedical engineering -- ResearchCartilage cellsActinCytoskeleton -- FormationCell differentiationCellular signal transduction -- Research -- MethodologyShear (Mechanics) -- AnalysisCell adhesion -- ResearchThesis