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Why and How Do Cells Sense Mechanical Load

Why and How Do Cells Sense Mechanical Load. Biophysics Frontiers 9/11/2013. Outline. Context of Cellular Biophysics / Mechanobiology Story of Brenton Hoffman Interesting aspects of mechanotransduction Studying Mechanotransduction

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Why and How Do Cells Sense Mechanical Load

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  1. Why and How Do Cells Sense Mechanical Load Biophysics Frontiers 9/11/2013

  2. Outline • Context of Cellular Biophysics / Mechanobiology • Story of Brenton Hoffman • Interesting aspects of mechanotransduction • Studying Mechanotransduction • Development and use of a FRET-based molecular tension sensor

  3. What is a Cell? • The basic functional units of life • Variety of cell types with distinct components, structures, and functions • Comprised of numerous components and structures • Topic of next couples classes One Cell (fertilized egg) Whole bunch of divisions 1013 specialized cells (human) Sea Urchin Mouse Seaweed

  4. A Cell to Biologist / Chemist “Cells are considered the basic units of life in part because they come in discrete and easily recognizable packages. That's because all cells are surrounded by a structure called the cell membrane. http://www.nature.com/scitable/topicpage/what-is-a-cell-14023083

  5. Corresponding Picture of a Human Oxygen Carbon Hydogen Nitrogen Calcium Phosphorous Other We have a characteristic shape A boundary (skin) Are made of characteristic set of elements Pretty effective picture, when you get sick, you get a pill

  6. A More Complete Picture of the Cell Organs: ER, Golgi, Nucleus… Skeleton and Muscles: Actin and Myosin Skin: Plasma Membrane

  7. Cell Migration: Cells generate forces Human neutrophil chasing bacteria and avoiding red blood cells

  8. Main Point • Traditionally cell regarded as largely biochemically-based system • Bags full of chemicals • Cells generate forces, so more to the story…

  9. The Story of Brenton Hoffman • 1997: Enrolled at Lehigh University • To play football • To study Chemical Engineering because, “I liked chemistry in high school, but really don’t want to spend all my time in a lab.” • 2001: Enrolled at University of Pennsylvania • Get PhD in Chemical Engineering • Interview: “I really want to do something practical. I think I will study the process control of industrial bioreactors. That way I can get a nice job at Merck.”

  10. The Story of Brenton Hoffman • First Week on campus, 2001: met Prof. John Crocker, a Polymer Physicist study cell mechanics • “I have no idea what this stuff is… This is awesome.” • Cell Mechanics • Cells resist deformation • Cells generate forces • Cells “sense” mechanical variables Generally, we don’t know how these processes work on the molecular level Very important in many disease states…

  11. Cell are not like “Normal” Materials Cells also generate forces, called active materials Heart Cells – Cardiomyocyte Courtesy of NenadBursac, Duke BME http://www.youtube.com/watch?v=SDWmVn6ScKI

  12. Cellular Microrheology Microrheology: the quantification of jiggle Cell Polymeric Material Particle motion is determined by Brownian motion and mechanical stiffness Particle motion is determined motor activity and mechanical stiffness

  13. Kinesin and dynein activity Observe molecular processes with microscopy Endogenous particles tracked with ~ 3 nm and 90 s spatial resolution Notice pulse-like temporal nature of the trafficking. Observe 8 nm steps, with some larger steps, exactly as expected

  14. The Story of Brenton Hoffman • 2005: Department changes its name to Chemical and Biomolecular Engineering • 2007: Finish PhD in Chemical and Biomolecular Engineering • Want to be a Professor • Need to do a Post-doc, but on what… Apply knowledge of cell mechanics to mechanotransduction

  15. What is Mechanotransduction?

  16. Mechanotransduction Conversion of mechanical stimuli (applied forces, shear stress, or extracellular rigidity) into biochemically detectable information Simplified Schematic of Rho GTPase regulation of actin structures Force Stress Mechanical Environment ? Academically interesting b/c we don’t know how it works

  17. Why study mechanotransduction? Force sensing is important in many disease states Atherogenesis Laminar Flow Atheroresistant Disturbed Flow Atheroprone Hahn, Nat Rev Mol Cell Bio, 2008 DeBakey, Annals of Surgery, 1985

  18. Why study mechanotransduction? Force sensing is important in many disease states Cancer Anyone know the primary means of identifying breast cancer? Butcher, Nat Rev Cancer, 2009

  19. Why study mechanotransduction? • Industrial Relevance • Tissue Engineering Manipulate cell behavior by controlling physical environment Mesenchymal stem cells plated on different rigidity substrates Engler, Cell, 2006

  20. Why studying Mechanotransduction? • Industrial Relevance: Tissue Engineering • A major problem in vascular engineering creating vessels that can withstand physical forces due to blood flow and support proper cell function • Current approaches copying the mechanical environment of the embryo • “Smooth muscles cells, which comprise vessel wall, were stimulated with pulsatile radial stress at 165 beats/min and 5% radial distension to mimic embryonic heart.”

  21. Bioreactors with Mechanical Stimulation Human muscle cells are attached to strands of collagen, or connective tissue. They are then subjected to cyclic stretching (“exercise”) in a bioreactor, which is a system designed to simulate the conditions of the human body. The pre-conditioning allows the cells to align in one direction, fuse to form muscle bundles, and function like normal muscle. http://www.wakehealth.edu/video/MultiMedia.aspx?id=38832

  22. Story of Brenton Hoffman • 2007: Starting Post-doc with Martin Schwartz, Physical Chemist PhD who is a world renown expert in Cell Biology and Mechanotransduction • Project: Make a molecular tension sensor

  23. Now Begin More Formal

  24. Mechanotransduction: Molecular Level How can force effect molecules? Conformational Change Hoffman, Nature, 2011

  25. Mechanotransduction: Cell Level What cellular structures bear force? Structural: Membrane and cytoskeleton Adhesive: Focal Adhesions and Cell-cell contacts Vascular Smooth Muscle Cell Structures are also signaling centers Hoffman, Nature, 2011

  26. Mechanotransduction: Cell Level Identified proteins that change activity level / localization in response to mechanical stimuli, such as Src Src Biosensor Force applied with laser trap through bead attached to integrins w/o force 1 min force 5 min force Wang, Nature, 2005

  27. Mechanotransduction: Molecular Level Talin Rod Cryptic Vinculin binding cites Vinculin Fluorescence Intensity Time (sec) Conversion of physical force into biochemical information Del Rio, Science, 2009

  28. Current Challenges What is relationship between single molecule events and cell behavior? When and where are forces exerted across proteins in cells? Are forces in cells large enough to cause conformation changes? ? Need Molecular Tension Sensor

  29. Outline • Design of a Molecular Tension Sensor • Picking the pieces • Calibration • Study of force mediated focal adhesion dynamics • Molecular tension across vinculin mediates focal adhesion assembly • On going projects

  30. Design Criteria • Genetically encoded • Applicable to multiple proteins • Analog Signal • Not just two state system • Sensitive to spatio-temporal variations • Reversible • Compatible with standard microscopy techniques • Sensitive to pico-Newton forces

  31. Picking the pieces: Technology Forster Resonance Energy Transfer Simple Picture FRET is exquisitely distance sensitive

  32. Argon Laser Lines 514 nm 458 nm Wavelength (nm) Picking the Pieces: Fluorophores Strongest, brightest genetically encoded FRET pair mTFP1 and Venus Forster Distance = 6.0 nm Cy3 – Cy5 = 6.0 nm Day, J Biomed Optics, 2008

  33. FRET Tension Sensor Concept A calibrated spring between two fluorophores would be a molecular tension sensor FRET is inversely related to force

  34. Picking the Pieces: Elastic Linker Design Criteria • Extremely extensible • Extremely Reversible • Modular (Length Control) • Known / understandable mechanical properties Flagelliform • Main Component of spider silk • Based on a five amino acid sequence • Weakly helical • Spider silk has been investigated with AFM and simulations • Responds to pN to nN forces Becker, Nat Mat, 2003

  35. Tension Sensing Module • Genetically encoded • Applicable to multiple proteins • Analog Signal • Sensitive to pico-Newton forces • Sensitive to spatio-temporal variations • Compatible with standard microscopy techniques

  36. Force Sensitivity Set by linker composition and length and properties of fluorophores Choose single molecule approach ? FRET Efficiency Force (pN)

  37. TSMod Calibration Empirical Conversion Analog Signal, Reversible, Force Sensitivity 1-6 pN TJ Ha, Micheal Brenner, and Ruobo Zhou, University of Illinois Grashoff, Hoffman, Nature, 2010

  38. Tension Sensing Module • Genetically encoded • Applicable to multiple proteins • Analog Signal • Sensitive to pico-Newton forces • Sensitive to spatio-temporal variations • Compatible with standard microscopy techniques

  39. Outline • Design of a Molecular Tension Sensor • Picking the pieces • Calibration • Study of force mediated focal adhesion dynamics • Molecular tension across vinculin mediates focal adhesion assembly • On going project • Next Generation Tension Sensors

  40. Cell migration is a multi-step process involving force generation and spatio-temporally regulated cell adhesion Leading Edge Picking a Problem Trailing Edge Important in many aspects of human health (wound healing, fighting infection…) human disease (metastatic cell migration, atheroslcerotic development…) Parsons, Nat Rev Mol Cell Bio, 2010

  41. Leading Edge Trailing Edge Picking a Problem Focal adhesions are mechano-sensitive sub-cellular structures that mediate cell adhesion and mechanotransduction Fluorescently labeled focal adhesions What is the molecular switch?

  42. Picking a Protein: Vinculin Function: Molecular Clutch Fast Actin Flow Slow Cell Movement Low Force Transmission Slow Actin Flow High Cell Movement High Force Transmission Cells must exert force to migrate. Forces are generated by F-actin cytoskeleton and transmitted through focal adhesions (FAs) to the extracellular matrix (ECM). Vinculin is a critical linkage in this process

  43. Vinculin Tension Sensor Grashoff, Hoffman, Nature, 2010

  44. Forces: FLIM-FRET of VinTS Calibration Average force across vinculin in stationary FAs is ~2.5 pN With Maddy Parsons, King’s College, London Grashoff, Hoffman, Nature, 2010

  45. Vinculin Tension During Cell Migration Individual FAs segmented and averaged FRET Index Migrating Bovine Aortic Endothelial Cells Low molecular tension at back is surprising Grashoff, Hoffman, Nature, 2010

  46. Force Across Vinculin Determines FA Dynamics Leading Edge High Tension Across Vinculin Low Tension Across Vinculin Trailing Edge

  47. Conclusions Have created a FRET-based molecular tension sensor for vinculin • Genetically encoded • Applicable to multiple proteins • Analog Signal • Sensitive to spatio-temporal variations • Compatible with standard microscopy techniques • Sensitive to pico-Newton forces

  48. Revealed an unexpected regulatory mechanism in which the ability of vinculin to bear force determines whether adhesions assemble or disassemble under tension. Conclusions High Tension Across Vinculin Low Tension Across Vinculin

  49. The Story of Brenton Hoffman • 2010: Publish this work in Nature • 2011: Wrote the review of Mechanotransduction you read • 2012: Start at Duke as a BME Prof.

  50. Lab Overview • Determining force-sensitive signaling pathways mediating focal adhesion dynamics • With tension sensor for the first time can see where a protein is under force. • Mapping relationship between protein tension and protein dynamics • Combining FRET and FRAP • How are do molecular forces across cellular adhesion structures mediate collective cell migration? • How are sources of applied force integrated?

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