Home > Seminars > The Design of Biomaterials to Investigate Healthy and Impaired Liver Function

The Design of Biomaterials to Investigate Healthy and Impaired Liver Function

Start:

11/8/2016 at 12:30PM

End:

11/8/2016 at 1:30PM

Location:

155 DeBartolo Hall

Host:

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Jeremiah Zartman

Jeremiah  Zartman

VIEW FULL PROFILE Email: jzartman@nd.edu
Phone: 574-631-0455
Website: http://www.nd.edu/~jzartman/
Office: 122C Cushing Hall

Affiliations

College of Engineering Assistant Professor
Bioengineering Graduate Program Assistant Professor
Developing new strategies for building tissues and treating degenerative tissue diseases requires investigating animal development from an engineering perspective. Probing animal development with quantitative tools can potentially improve traditional methods of tissue engineering as well as ...
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The liver plays a critical role in metabolism, biotransformation and detoxification. The design of in vitro models that mimic the stratified multi-cellular hepatic structure continues to be challenging. Hepatic cells rapidly lose their functions in culture, underscoring the need to recreate their microenvironment found in vivo. We have assembled a novel 3D organotypic liver model incorporating three different primary cell types (hepatocytes, liver sinusoidal endothelial, and Kupffer cells) and a polymeric membrane that mimics the Space of Disse. The polymeric membranes are detachable, optically transparent, and derived from self-assembled biopolymer multilayers. The mechanical properties of the polymeric membranes can be varied to mimic basement membranes that exhibit a wide range of physical properties. In our studies, only the 3D liver models simultaneously maintained hepatic phenotype and elicited proliferation while achieving cellular ratios found in vivo. Ongoing investigations using these liver models are focused on understanding inter-cellular communications between hepatic parenchymal and non-parenchymal cells, and, responsiveness to toxicants.

Chronic liver diseases, often associated with alcoholism, hepatitis and other health conditions can lead to hepatic fibrosis and eventually cirrhosis. As hepatic fibrosis occurs, an abundance of extracellular matrix proteins are produced. This buildup of proteins causes changes in the liver microarchitecture and can result in a six-fold increase in liver stiffness. We are designing biomaterial substrates that mimic fibrotic liver tissues. We are investigating the effects of substrate elasticity on liver endothelial cell function. Our results demonstrate changes in endothelial cell fenestrae diameter, stellate cell markers and hepatic function.

Seminar Speaker:

Padma Rajagopalan

Padma Rajagopalan

Virginia Tech

Dr. Rajagopalan is the Robert E. Hord Jr. Professor in the Department of Chemical Engineering at Virginia Tech. She is a core faculty member in the School of Biomedical Engineering and Sciences. Dr. Rajagopalan earned her bachelor’s degree from the Indian Institute of Technology, Kharagpur, India and obtained her Ph.D. from Brown University.   In 2010, Dr. Rajagopalan was the recipient of the NSF Faculty Early Career Development Award (CAREER).  She currently serves as the co-director for the Center on Systems Biology of Engineered Tissues and as the Program Director for an Interdisciplinary Graduate Education Program on Computational Tissue Engineering. 

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