Engineering Stem Cell Microenvironments

Author: ccrosby (Page 4 of 6)

The Zoldan Lab Welcomes Christine Wei!

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The Zoldan Lab welcomes Christine Wei, a junior at UT Austin who will be helping Cody Crosby and Julie Strickland with the development of their hydrogel-liposome system.

I wanted to join the Zoldan Lab, because of its work with stem cell research. This research has so much potential, and even the smallest amount of progress in understanding these cells will be revolutionary in the medical field. In this lab, I hope to better understand how stem cells function and react, and to help work toward developing medical applications that can help patients in the future- Christine Wei

Chengyi publishes in Integrative Biology!

Congratulations to Chengyi Tu, who published his work “Monitoring protein synthesis in live cancer cells” in the journal Integrative Biology. The abstract is shown below:

Protein synthesis is generally under sophisticated and dynamic regulation to meet the ever-changing demands of a cell. Global up or down-regulation of protein synthesis and the shift of protein synthesis location (as shown, for example, during cellular stress or viral infection) are recognized as cellular responses to environmental changes such as nutrient/oxygen deprivation or to alterations such as pathological mutations in cancer cells. Monitoring protein synthesis in single live cells can be a powerful tool for cancer research. Here we employed a microfluidic platform to perform high throughput delivery of fluorescent labeled tRNAs into multiple myeloma cells with high transfection efficiency (∼45%) and high viability (>80%). We show that the delivered tRNAs were actively recruited to the ER for protein synthesis and that treatment with puromycin effectively disrupted this process. Interestingly, we observed the scattered distribution of tRNAs in cells undergoing mitosis, which has not been previously reported. Fluorescence lifetime analysis detected extensive FRET signals generated from tRNAs labeled as FRET pairs, further confirming that the delivered tRNAs were used by active ribosomes for protein translation. Our work demonstrates that the microfluidic delivery of FRET labeled tRNAs into living cancer cells can provide new insights into basic cancer metabolism and has the potential to serve as a platform for drug screening, diagnostics, or personalized medication.


Zoldan Lab participates in Explore UT!

The Zoldan Lab participated in Explore UT, an event meant to showcase the University of Texas at Austin’s education, research, and outreach. The lab members presented on the interaction of stem cells and biomaterials and how this research might be leveraged to create personalized stem cell therapies. Highlights included the exhibition of beating cardiomyocytes and a working cotton candy machine (to explain fiber extrusion). FullSizeRender (5)

iPSC-Derived Tissue Constructs

Challenges in the field of iPSCs-derived tissue engineering include the construction of thick and complex tissue structures. Combining therapies using iPSCs and growth factor release from polymeric scaffolds tailored to promote angiogenesis and cardiogenesis, we develop vascularized cardiac grafts for therapeutic applications.  The pluripotency of stem cells is used to create multi-cellular tissue-structures and induce tissue organization during cellular differentiation.

TissueConstructs

Mimicking the Cardiac Niche

CardiacNicheWe design 3D-engineered matrices which tune physical, chemical, and biological properties such as control signals, to create a cellular microenvironment better representative of natural developmental processes. We study how these physical cues guide complex behavior such as stem cell differentiation and work to determine the role of cytoskeleton and adhesion sites in these processes.

Directing iPSC Differentiation

Utilizing a unique microfluidic device to deliver proteins into the cytoplasm of iPSCs, we direct iPSC differentiation into cardiac lineages to develop safe, efficient, and robust production of patient-specific cell lines for cell replacement therapies and cardiovascular tissue engineering applications. The microfluidic device contains constrictions which induce membrane pore formation in stem cells due to rapid mechanical deformation, allowing for cytosolic protein delivery. Delivered proteins will be chosen by proteomic analysis of cardiovascular lineages and derivation of protein interactions maps.

DirectingiSPCDiff

Undergraduate Students

Shreya Ramesh

B.S. Biomedical Engineering (in progress)
The University of Texas at Austin

shreyar@utexas.edu

Jasmine Pok

B.S. Biomedical Engineering (in progress)
The University of Texas at Austin

socheatapok@utexas.edu

Katelyn Dockery

B.S. Biomedical Engineering (in progress)
The University of Texas at Austin

katelyndockery@utexas.edu

Ali Moshin

B.S. Biomedical Engineering (in progress)
The University of Texas at Austin

alimohsin2000jp@utexas.edu

Postdoctoral Scholars

Dr. Nima Momtahan

Ph.D. Biomedical Engineering,
Brigham Young University

nima.momtahan@gmail.com

Project: Biomaterials and Cardiac Tissue Engineering.

Fun Fact: When I want people to remember my name, I say my name is Nima, like Nemo the fish!

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