Kim:Research

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<font face="trebuchet ms" size=4 style="color:#000">'''Research Overview: </font> <br> </div>
<font face="trebuchet ms" size=4 style="color:#000">'''Research Overview: </font> <br> </div>
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Our research focuses on investigating how the engineered microenvironments direct cell function and tissue regeneration. In particular, we are exploring extracellular matrix (topology, rigidity, dimensionality, etc) regulation of cell fate and function in developmental, physiological and pathological process. Several specific thrusts of the current research program include: microscale cardiovascular tissue engineering, BioMEMS for stem/progenitor cell niche engineering, microengineered platforms for cell-matrix mechanobiology, and mechanical regulation of cancer cell invasion and collective cell migration.  Here is a summary of our current research projects.  
Our research focuses on investigating how the engineered microenvironments direct cell function and tissue regeneration. In particular, we are exploring extracellular matrix (topology, rigidity, dimensionality, etc) regulation of cell fate and function in developmental, physiological and pathological process. Several specific thrusts of the current research program include: microscale cardiovascular tissue engineering, BioMEMS for stem/progenitor cell niche engineering, microengineered platforms for cell-matrix mechanobiology, and mechanical regulation of cancer cell invasion and collective cell migration.  Here is a summary of our current research projects.  
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<font face="trebuchet ms" size=4 style="color:#000">'''Technological:</font>  <font face="trebuchet ms" size=4 style="color:#00688B">Development of biomimetic cell/tissue microenvironments using micro and nano engineering techniques</font> <br> </div>
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<font face="trebuchet ms" size=4 style="color:#000">'''Technological:</font>  <font face="trebuchet ms" size=4 style="color:#00688B"> Biologically inspired, biomimetic materials, microsystems and cell/tissue microenvironments</font> <br> </div>
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Our current research focuses on engineering combinatorial cellular microenvironment through use of variable nano-patterns, and soluble and matrix-bound cell guidance cues in a single experiment, which better mimics the in vivo microenvironment under physiological conditions. For example, we are developing a microfluidics-based on chip assay integrated with complex nanoscale  topographic features to enable the analysis of concerted cell responses to composite gradients of precisely generated and aligned surface-bound ECM molecules and diffusible guidance cues or topographic guidance cues. Using these tools, we strive to systematically characterize live cells to wide spectra of dynamically changing combination of mechanical and chemical stimuli (e.g. ECM proteins, topographic, growth factors and signal transduction pathway inhibitors). The proposed measurements are highly resolved in time and space, using a variety of live cell probes and highly defined extracellular conditions. Using UV-assisted nanomolding and 3D nanofabrication techniques, we are developing nanotopographically-defined cell culture models and biomaterial tissue scaffolds for cell biology and tissue engineering. For high-throughput quantitative analysis, we are also working to combine a large area nanopatterned substrate with a traditional multi-well tissue culture plate. We aim to use these tools to gain new mechanistic insights into cell signaling and function, to design new therapies or diagnostic tests for cancer progression and cardiovascular diseases, and to establish organizing principles for development of precisely defined scaffolds for advanced tissue engineering applications.  
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Micro- and nanoengineering for stem cell biology: the promise with a caution (''Trends Biotechnol.'' '''29(8)''', 399-408 [2011])]]Our current research focuses on engineering combinatorial cellular microenvironment through use of variable nano-patterns, and soluble and matrix-bound cell guidance cues in a single experiment, which better mimics the in vivo microenvironment under physiological conditions. For example, we are developing a microfluidics-based on chip assay integrated with complex nanoscale  topographic features to enable the analysis of concerted cell responses to composite gradients of precisely generated and aligned surface-bound ECM molecules and diffusible guidance cues or topographic guidance cues. Using these tools, we strive to systematically characterize live cells to wide spectra of dynamically changing combination of mechanical and chemical stimuli (e.g. ECM proteins, topographic, growth factors and signal transduction pathway inhibitors). The proposed measurements are highly resolved in time and space, using a variety of live cell probes and highly defined extracellular conditions. Using UV-assisted nanomolding and 3D nanofabrication techniques, we are developing nanotopographically-defined cell culture models and biomaterial tissue scaffolds for cell biology and tissue engineering. For high-throughput quantitative analysis, we are also working to combine a large area nanopatterned substrate with a traditional multi-well tissue culture plate. We aim to use these tools to gain new mechanistic insights into cell signaling and function, to design new therapies or diagnostic tests for cancer progression and cardiovascular diseases, and to establish organizing principles for development of precisely defined scaffolds for advanced tissue engineering applications.
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Micro- and nanoengineering for stem cell biology: the promise with a caution (''Trends Biotechnol.'' '''29(8)''', 399-408 [2011])]]
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<font face="trebuchet ms" size=4 style="color:#000">'''Fundamental:</font>  <font face="trebuchet ms" size=4 style="color:#00688B"> Cellular mechanobiology and mechanotransduction in engineered tissue models </font> <br> </div>
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[[Image:Fundamental.gif|thumb|250x250px|Microengineered Platforms for Cell Mechanobiology (''Annu Rev Biomed Eng'' '''11''', 203-233 [2009])]]
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<font face="trebuchet ms" size=4 style="color:#000">'''Fundamental:</font>  <font face="trebuchet ms" size=4 style="color:#00688B"> Mechanobiology and mechanotransduction in engineered tissue models </font> <br> </div>
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[[Image:ADDR_Image.jpg|left|thumb|250x250px|Nanotopography-guided tissue engineering and regenerative medicine (''Advanced Drug Delivery Reviews'' '''65''', 536-558 [2013])]]<font size = 3>
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Mechanotransduction - from how cells sense mechanical forces in different tissues to how these mechanical forces are transduced into biochemical signals - is an essential biological process in development, normal physiology and disease. In this exciting area, we are particularly interested in investigating the role of mechano-biological processes associated with cell-cell and cell-matrix  adhesions (e.g. topography and rigidity of the extracellular matrix) in the regulation of collective and directed cell migration and tissue morphogenesis. Using a combination of various techniques, from molecular biology to nanotechnology and live cell imaging, for example, we have been accumulating interesting data suggesting that one of the most important factors distinguishing metastatic from non-metastatic cells could be their ability to collectively invade and migrate towards blood vessels by physically interacting with the surrounding extracellular matrices.  By experimenting with the nanotopographically-defined cell adhesion substratum (i.e. quasi 3D cell culture system) and 3D natural/synthetic extracellular matrices, we are investigating the biophysical and signaling mechanisms of collective cell migration driven by the hypothesis that the physical interaction of migrating cells with the surrounding ECM has a crucial role in the collective guidance of cell migration in the context of cancer invasion and wound healing. To test this hypothesis, we recently developed a micro/nanofabricated collective migration assay as an enabling tool for analysis and control of cancer cell invasion and epithelial/endothelial wound healing in a high-throughput, controlled manner. Using these tools, we also explore the potential role of mechanical guidance in the regulation of collective cell migration and tissue morphogenesis under the presence/absence of growth factor-induced signals, and test their biomedical implication by screening cytoskeletal and signal transduction pathways.
Mechanotransduction - from how cells sense mechanical forces in different tissues to how these mechanical forces are transduced into biochemical signals - is an essential biological process in development, normal physiology and disease. In this exciting area, we are particularly interested in investigating the role of mechano-biological processes associated with cell-cell and cell-matrix  adhesions (e.g. topography and rigidity of the extracellular matrix) in the regulation of collective and directed cell migration and tissue morphogenesis. Using a combination of various techniques, from molecular biology to nanotechnology and live cell imaging, for example, we have been accumulating interesting data suggesting that one of the most important factors distinguishing metastatic from non-metastatic cells could be their ability to collectively invade and migrate towards blood vessels by physically interacting with the surrounding extracellular matrices.  By experimenting with the nanotopographically-defined cell adhesion substratum (i.e. quasi 3D cell culture system) and 3D natural/synthetic extracellular matrices, we are investigating the biophysical and signaling mechanisms of collective cell migration driven by the hypothesis that the physical interaction of migrating cells with the surrounding ECM has a crucial role in the collective guidance of cell migration in the context of cancer invasion and wound healing. To test this hypothesis, we recently developed a micro/nanofabricated collective migration assay as an enabling tool for analysis and control of cancer cell invasion and epithelial/endothelial wound healing in a high-throughput, controlled manner. Using these tools, we also explore the potential role of mechanical guidance in the regulation of collective cell migration and tissue morphogenesis under the presence/absence of growth factor-induced signals, and test their biomedical implication by screening cytoskeletal and signal transduction pathways.
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<font face="trebuchet ms" size=4 style="color:#000">'''Translational:</font>  <font face="trebuchet ms" size=4 style="color:#00688B"> Stem cell niche engineering and functional tissue engineering </font> <br> </div>
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<font face="trebuchet ms" size=4 style="color:#000">'''Translational:</font>  <font face="trebuchet ms" size=4 style="color:#00688B"> Microenvironmental stem cell niche engineering and functional tissue engineering </font> <br> </div>
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With advances in nanofabrication and biomaterials, scaffolding materials can be designed to integrate biomimetic structural and mechanical cues present in the in vivo ECM environment. Based on ultrastructural analyses of the native heart tissue, we are developing a bio-inspired model cardiac tissue to better understand cardiac tissue structure-function relationships, and to seek applications in stem cell-based therapies for cardiac tissue repair and regeneration. The ultimate goal of this project is to develop nanopatterned functional cardiac patches for treating the damaged heart tissue (e.g. myocardial infarction). The working hypothesis is that cultivation of cardiac cells and/or stem cells on novel biomaterials scaffolds integrated with nanotopographic cues promotes biomimetic anisotropic assembly of uniformly contractile engineered muscle, while simultaneously enabling control over local cell alignment. We further envision that integrating the transplantable stem cells with the proposed nano-grafting techniques have therapeutic potential in repairing cardiac tissue damage and may prevent the onset of heart failure. In order to test these hypotheses, our research focuses on elucidating the relationships between scaffold-mediated nanostructural cues and tissue engineered cardiac graft contractility and function. In addition, the therapeutic potential of a nanopatterned cardiac stem cell graft will be studied in vitro and in vivo (implantation onto the left ventricle in an adult rat model of myocardial infarction). Tissue structure and function will be characterized at various hierarchical scales (molecular, structural, functional) and the obtained experimental data will be used to tailor the conditions and duration of cultivation, leading to engineering implantable grafts.  
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[[Image:Translational.tif|thumb|200x200px|Nanoscale cues regulate the structure and function of macroscopic cardiac tissue constructs (''PNAS'' '''107''', 565-570 [2010])]]With advances in nanofabrication and biomaterials, scaffolding materials can be designed to integrate biomimetic structural and mechanical cues present in the in vivo ECM environment. Based on ultrastructural analyses of the native heart tissue, we are developing a bio-inspired model cardiac tissue to better understand cardiac tissue structure-function relationships, and to seek applications in stem cell-based therapies for cardiac tissue repair and regeneration. The ultimate goal of this project is to develop nanopatterned functional cardiac patches for treating the damaged heart tissue (e.g. myocardial infarction). The working hypothesis is that cultivation of cardiac cells and/or stem cells on novel biomaterials scaffolds integrated with nanotopographic cues promotes biomimetic anisotropic assembly of uniformly contractile engineered muscle, while simultaneously enabling control over local cell alignment. We further envision that integrating the transplantable stem cells with the proposed nano-grafting techniques have therapeutic potential in repairing cardiac tissue damage and may prevent the onset of heart failure. In order to test these hypotheses, our research focuses on elucidating the relationships between scaffold-mediated nanostructural cues and tissue engineered cardiac graft contractility and function. In addition, the therapeutic potential of a nanopatterned cardiac stem cell graft will be studied in vitro and in vivo (implantation onto the left ventricle in an adult rat model of myocardial infarction). Tissue structure and function will be characterized at various hierarchical scales (molecular, structural, functional) and the obtained experimental data will be used to tailor the conditions and duration of cultivation, leading to engineering implantable grafts.  
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<font size = 3> '''Funding Sources''':
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<font size = 3>Our research would not be possible without the the generous support of the following public and private organizations. <br>
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[[Image:Translational.tif|thumb|180x180px|Nanoscale cues regulate the structure and function of macroscopic cardiac tissue constructs (''PNAS'' '''107''', 565-570 [2010])]]
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<font size = 3> '''Funding Sources''': <br>
 
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<font size = 2>Our research would not be possible without the the generous support of the following public and private organizations. <br>
 
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[[Image:KSEAlogo.jpg|200px|link = http://www.ksea.org/2013/]] &emsp;&emsp; <br>
 

Revision as of 04:57, 6 April 2014

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Research Overview:

Our research focuses on investigating how the engineered microenvironments direct cell function and tissue regeneration. In particular, we are exploring extracellular matrix (topology, rigidity, dimensionality, etc) regulation of cell fate and function in developmental, physiological and pathological process. Several specific thrusts of the current research program include: microscale cardiovascular tissue engineering, BioMEMS for stem/progenitor cell niche engineering, microengineered platforms for cell-matrix mechanobiology, and mechanical regulation of cancer cell invasion and collective cell migration. Here is a summary of our current research projects.

Technological: Biologically inspired, biomimetic materials, microsystems and cell/tissue microenvironments
Micro- and nanoengineering for stem cell biology: the promise with a caution (Trends Biotechnol. 29(8), 399-408 [2011])
Micro- and nanoengineering for stem cell biology: the promise with a caution (Trends Biotechnol. 29(8), 399-408 [2011])
Our current research focuses on engineering combinatorial cellular microenvironment through use of variable nano-patterns, and soluble and matrix-bound cell guidance cues in a single experiment, which better mimics the in vivo microenvironment under physiological conditions. For example, we are developing a microfluidics-based on chip assay integrated with complex nanoscale topographic features to enable the analysis of concerted cell responses to composite gradients of precisely generated and aligned surface-bound ECM molecules and diffusible guidance cues or topographic guidance cues. Using these tools, we strive to systematically characterize live cells to wide spectra of dynamically changing combination of mechanical and chemical stimuli (e.g. ECM proteins, topographic, growth factors and signal transduction pathway inhibitors). The proposed measurements are highly resolved in time and space, using a variety of live cell probes and highly defined extracellular conditions. Using UV-assisted nanomolding and 3D nanofabrication techniques, we are developing nanotopographically-defined cell culture models and biomaterial tissue scaffolds for cell biology and tissue engineering. For high-throughput quantitative analysis, we are also working to combine a large area nanopatterned substrate with a traditional multi-well tissue culture plate. We aim to use these tools to gain new mechanistic insights into cell signaling and function, to design new therapies or diagnostic tests for cancer progression and cardiovascular diseases, and to establish organizing principles for development of precisely defined scaffolds for advanced tissue engineering applications.
Fundamental: Cellular mechanobiology and mechanotransduction in engineered tissue models
Nanotopography-guided tissue engineering and regenerative medicine (Advanced Drug Delivery Reviews 65, 536-558 [2013])
Nanotopography-guided tissue engineering and regenerative medicine (Advanced Drug Delivery Reviews 65, 536-558 [2013])
Mechanotransduction - from how cells sense mechanical forces in different tissues to how these mechanical forces are transduced into biochemical signals - is an essential biological process in development, normal physiology and disease. In this exciting area, we are particularly interested in investigating the role of mechano-biological processes associated with cell-cell and cell-matrix adhesions (e.g. topography and rigidity of the extracellular matrix) in the regulation of collective and directed cell migration and tissue morphogenesis. Using a combination of various techniques, from molecular biology to nanotechnology and live cell imaging, for example, we have been accumulating interesting data suggesting that one of the most important factors distinguishing metastatic from non-metastatic cells could be their ability to collectively invade and migrate towards blood vessels by physically interacting with the surrounding extracellular matrices. By experimenting with the nanotopographically-defined cell adhesion substratum (i.e. quasi 3D cell culture system) and 3D natural/synthetic extracellular matrices, we are investigating the biophysical and signaling mechanisms of collective cell migration driven by the hypothesis that the physical interaction of migrating cells with the surrounding ECM has a crucial role in the collective guidance of cell migration in the context of cancer invasion and wound healing. To test this hypothesis, we recently developed a micro/nanofabricated collective migration assay as an enabling tool for analysis and control of cancer cell invasion and epithelial/endothelial wound healing in a high-throughput, controlled manner. Using these tools, we also explore the potential role of mechanical guidance in the regulation of collective cell migration and tissue morphogenesis under the presence/absence of growth factor-induced signals, and test their biomedical implication by screening cytoskeletal and signal transduction pathways.
Translational: Microenvironmental stem cell niche engineering and functional tissue engineering

Nanoscale cues regulate the structure and function of macroscopic cardiac tissue constructs (PNAS 107, 565-570 [2010])
Nanoscale cues regulate the structure and function of macroscopic cardiac tissue constructs (PNAS 107, 565-570 [2010])
With advances in nanofabrication and biomaterials, scaffolding materials can be designed to integrate biomimetic structural and mechanical cues present in the in vivo ECM environment. Based on ultrastructural analyses of the native heart tissue, we are developing a bio-inspired model cardiac tissue to better understand cardiac tissue structure-function relationships, and to seek applications in stem cell-based therapies for cardiac tissue repair and regeneration. The ultimate goal of this project is to develop nanopatterned functional cardiac patches for treating the damaged heart tissue (e.g. myocardial infarction). The working hypothesis is that cultivation of cardiac cells and/or stem cells on novel biomaterials scaffolds integrated with nanotopographic cues promotes biomimetic anisotropic assembly of uniformly contractile engineered muscle, while simultaneously enabling control over local cell alignment. We further envision that integrating the transplantable stem cells with the proposed nano-grafting techniques have therapeutic potential in repairing cardiac tissue damage and may prevent the onset of heart failure. In order to test these hypotheses, our research focuses on elucidating the relationships between scaffold-mediated nanostructural cues and tissue engineered cardiac graft contractility and function. In addition, the therapeutic potential of a nanopatterned cardiac stem cell graft will be studied in vitro and in vivo (implantation onto the left ventricle in an adult rat model of myocardial infarction). Tissue structure and function will be characterized at various hierarchical scales (molecular, structural, functional) and the obtained experimental data will be used to tailor the conditions and duration of cultivation, leading to engineering implantable grafts.


Funding Sources:
Our research would not be possible without the the generous support of the following public and private organizations.

link="http://mda.org/"    link = http://www.nih.gov/    link = http://www.heart.org/HEARTORG/    link=http://mda.org/    link=http://www.mke.go.kr/language/eng/   
link =http://www.whcf.org/    link = http://depts.washington.edu/uwc4c/      link = http://www.lsdfa.org/    link = http://www.washington.edu/    link = http://www.ksea.org/2013/   

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