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Stem cell functions are regulated by local cues present in their microenvironment including soluble growth factors,
extracellular matrix (ECM), cell-cell interactions, as well as mechanical signals such as the matrix rigidity. While the effect of individual type
of microenvironmental cues on stem cell behavior has been studied in great depth, little is known about how the complex interplay of multiple types
of signals would influence stem cell behavior. We are interested in understanding the effects of interactive signaling on stem cell in 3D and results
from such studies would help predict stem cell phenotype in vivo and direct rational design of stem cell niche for tissue engineering applications. |
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Advances in gene therapy provide a powerful tool to promote lineage-specific differentiation via directly
regulating the intrinsic signals of stem cells. Today, technology is being developed with the potential to either “turn on” a target gene,
through DNA delivery, or “turn off” a gene by siRNA delivery. However, such therapy has rarely found its way into the clinic due to the lack
of safe and efficient delivery systems that can stably regulate stem cells in vivo. Our goal is to develop a controlled release system
for sustained delivery of synergistic genetic signals to direct stem cells differentiation in situ. |
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Many disease processes are associated with abnormal blood supply, cell death and eventual loss of tissue structure and function.
Delivery of therapeutic factors directly to the affected tissues may intervene with the disease progression and start the tissue repair. However, effective targeting
and delivery to the disease site remains a great challenge. We are interested in engineering stem cells for targeting and delivery of therapeutic factors to restore normal vascularization and promote
tissue regeneration. Findings from such study would have great translational potential that may benefit patients in the future.
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