Fischell Department of Bioengineering

Permanent URI for this communityhttp://hdl.handle.net/1903/6626

null

Browse

Subject: search.filters.subject.tissue engineering

Search Results

Now showing 1 - 3 of 3
  • Thumbnail Image
    Item
    Engineering Cell Surfaces with Polyelectrolyte Materials for Translational Applications
    (MDPI, 2017-01-28) Zhang, Peipei; Bookstaver, Michelle L.; Jewell, Christopher M.
    Engineering cell surfaces with natural or synthetic materials is a unique and powerful strategy for biomedical applications. Cells exhibit more sophisticated migration, control, and functional capabilities compared to nanoparticles, scaffolds, viruses, and other engineered materials or agents commonly used in the biomedical field. Over the past decade, modification of cell surfaces with natural or synthetic materials has been studied to exploit this complexity for both fundamental and translational goals. In this review we present the existing biomedical technologies for engineering cell surfaces with one important class of materials, polyelectrolytes. We begin by introducing the challenges facing the cell surface engineering field. We then discuss the features of polyelectrolytes and how these properties can be harnessed to solve challenges in cell therapy, tissue engineering, cell-based drug delivery, sensing and tracking, and immune modulation. Throughout the review, we highlight opportunities to drive the field forward by bridging new knowledge of polyelectrolytes with existing translational challenges.
  • Thumbnail Image
    Item
    DETERMINING THE EFFECT OF EXTRACELLULAR MICROENVIRONMENT ON TROPHOBLAST INVASION USING A BIOPRINTED PLACENTA MODEL
    (2017) Kuo, Che-Ying; Fisher, John P; Kim, Peter CW; Bioengineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Preeclampsia is a leading cause of maternal and perinatal morbidity and mortality, affecting 8% of all pregnancies. Currently, the only effective treatment for preeclampsia is the premature delivery of the fetus and placenta resulting in significant fetal morbidity. In early pregnancy, fetal trophoblast cells invade and remodel maternal spiral arteries in the uterine wall to create the high capacitance organ of placenta. The uterine spiral arteries in preeclampsia, however, remain narrow and poorly remodeled. The exact mechanisms of how trophoblast invade and remodel the spiral arteriole are not known, and there is a paucity of relevant experimental models to study the mechanisms in human pregnancy. The goal of this work was to develop a dynamic bioprinted placenta model and use it to determine the role of extracellular microenvironment in preeclampsia. We began by developing a 3D placenta model that could quantify trophoblast invasion rates through bioprinting. Then we used decellularization techniques to isolate and established the necessary role of placental basement membrane protein to achieve effective trophoblast invasion. Finally, we used the dynamic bioprinted placenta model and found trophoblast impairs the flow-induced angiogenesis of endothelial cells, a process that plays a central role in preeclampsia. Overall, we described the significant impact of the extracellular microenvironment on the behavior trophoblast and/or endothelial cells, an area that is less investigated but appeared to be critical in the pathogenesis of preeclampsia. Moreover, the approach presented in this work can be used to screen and develop novel therapeutics and biomarkers not only for preeclampsia but also other diseases such as cancer metastasis and wound healing.
  • Thumbnail Image
    Item
    ORBITAL FLOOR REGENERATION USING CYCLIC ACETAL HYDROGELS THROUGH ENHANCED OSTEOGENIC CELL SIGNALING OF MESENCHYMAL STEM CELLS
    (2009) Betz, Martha Wheaton; Fisher, John P; Bioengineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Orbital floor fractures are a serious consequence of craniofacial trauma and account for approximately 60-70% of all orbital fractures. Unfortunately, the body's natural response to orbital floor defects generally does not restore proper function and facial aesthetics which is complicated by the thin bone and adjacent sinuses. We propose using a tissue engineering strategy to regenerate orbital floor bone. To this end, a functional biomaterial was investigated to enhance orbital floor regeneration. First, a bone marrow stromal cell population was isolated and differentiation assessed via coculture with chondrocytes and osteogenic media supplements. A cyclic acetal biomaterial composed of the cyclic acetal monomer 5-ethyl-5-(hydroxymethyl)-β,β-dimethyl-1,3-dioxane-2-ethanol diacrylate (EHD) and poly(ethylene glycol) diacrylate (PEGDA) was then developed for cell encapsulation. The previously investigated bone marrow stromal cells were then used to determine the effects of the ammonium persulfate/N,N,N',N'-tetramethylethylenediamine initiator system used to crosslink the EH-PEG hydrogels on cell viability, metabolic activity, and osteogenic differentiation. Next, EH-PEG hydrogels were implanted into orbital floor defects with bone morphogenetic protein-2, where tissue response and surrounding bone growth was analyzed. To improve surrounding tissue interaction and cell infiltration, macroporous EH-PEG hydrogels were created using porogen-leaching. These hydrogels were characterized using optical coherence tomography for pore size, porosity, and cell viability. In addition, these macroporous hydrogels were created with varying architecture to analyze the effects on osteogenic signaling and differentiation. This work outlines the potential application of EH-PEG hydrogels for use in orbital floor repair.