|
|
| (5 intermediate revisions by the same user not shown) |
| Line 4: |
Line 4: |
| |width=735px class="MainPageBG" style="border: 5px solid #330000; color: #000000; background-color: #FFFFFF"| | | |width=735px class="MainPageBG" style="border: 5px solid #330000; color: #000000; background-color: #FFFFFF"| |
| <div style="padding: .4em .9em .9em"> | | <div style="padding: .4em .9em .9em"> |
| __NOTOC__
| |
| == Matrix Physicochemical Cues as Chemotherapeutic Protective Agents in Hepatocellular Carcinoma ==
| |
| ''Thuy Nguyen''<br>
| |
| Thuy is building a highthroughput biomaterial system in which to quantify how cancer cells respond to drugs in the presence of physiologically relevent stiffness and adhesive protein cues.
| |
|
| |
|
| [[Image:Thuy_wordle.jpg|left|300px]]
| | ==We Have Moved!== |
| [[Image:PhRMA.jpg|right|300px]]
| |
|
| |
|
| <br>
| | Check out [http://www.peytonlab.org Peytonlab.Org] |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| | |
| | |
| | |
| | |
| | |
| | |
| == Inflammatory Feedback Loops in Cardiovascular Disease ==
| |
| ''Will Herrick''<br>
| |
| '''Funding: ICE IGERT'''<br>
| |
| We are investigating the ability of matrix state to trigger SMC motility and invasion via stiffness changes during atherosclerosis and the presence of infiltrating macrophages.
| |
| | |
| [[Image:Will_wordle.jpg|left|300px]] | |
| [[Image:EAM_SETUP.png|right|300px]]
| |
| | |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| | |
| == Stiffness Sensing as a Metastatic Indicator ==
| |
| ''Dannielle Ryman, in collaboration with Al Crosby in PSE''<br>
| |
| '''Funding: MRSEC'''<br>
| |
| We are working with Yuri Ebata and Yujie Liu from Al Crosby's lab in PSE to make novel substrates with unique presentation of stiffness arrays and mechanical length scales. We are visualizing how breast cancer cells of varying known metastatic capability sense and respond (namely, migration and mitosis) to these changes in stiffness.
| |
| | |
| [[Image:DRyman_Screenshot.png|center|200px]]
| |
| | |
| == Predicting Tissue Tropism in Metastasis ==
| |
| ''Lauren Barney and Erinn Dandley, in Collaboration with Todd Emrick in PSE and Nick Reich in Public Health''<br>
| |
| Erinn and Lauren are creating both 2D and 3D models of tissues that are most often recipient of breast cancer metastasis. They are quantifying how breast cancer cells migrate and invade in these diverse environments, in the hope that we can identify physical mechanisms by which breast cancer spreads.
| |
| | |
| [[Image:NSF_PESO_wordle.jpg|left|300px]]
| |
| [[Image:NSF_PESO_intro.png|right|350px]]
| |
| | |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| <br>
| |
| | |
| == Anomalous Diffusion Methods to Predict 3D Stem Cell Motility in Porous Scaffolds ==
| |
| ''Tyler Vlass, in Collaboration with Josh Cohen at MIT and Ryan Hayward in PSE''<br>
| |
| Tyler and Josh are both outstanding undergraduates that the Peyton lab is lucky to work with. Tyler is leading experimental efforts to quantify how adult stem cells migrate in response to physical properties of 2D and 3D scaffolds. Josh works with us from MIT and is developing new computational approaches to describe and predict stem cell migration in these scaffolds.
| |
| | |
| [[Image:MSC_Peyton_wordle.tiff|left|300px]]
| |
| [[Image:3D_scaffold.jpg|center|300px]]
| |
