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Live Cell Imaging to Investigate Bone Marrow Stromal Cell Adhesion and Migration on Titanium Surfaces: A Micro-Incubator in vitro Model

Jensen, Rebecca Leah

Abstract Details

2013, Master of Science in Chemical Engineering, Cleveland State University, Fenn College of Engineering.
Under this research, live cell imaging of osteoblast-like marrow stromal cells has been carried out on polished and nanotextured (NaOH-etched) medical-grade titanium alloy (Ti-6Al-4V) surfaces to examine cellular adhesion and migration. The purpose of this research was to: 1) Build and assemble suitable hardware and software to conduct live cell imaging in a micro-incubator over an extended period of time. 2) Monitor and record live osteoblast-like marrow stromal cells on polished and NaOH-etched titanium alloy surfaces from cell inoculation to about one week of culture. 3) Measure location, area and perimeter of individual cells as a function of time, and examine if, as compared / contrasted with the polished titanium surface, that the NaOH-etched titanium surface promotes adhesion and migration of cells. This was achieved by describing the mobility, morphology and overall behavior of osteoblast-like marrow stromal cells. During the cell growth cycles, data generated from image analysis included the cells’ center of mass (X,Y), their area, perimeter and shape as a function of incubation time. From the change in center of mass after each 15-minute interval, the real time speed of the cells was obtained. Major observations to support comparison studies between the surfaces determined that compared with polished titanium, NaOH-etched titanium promotes cellular filopodia growth, thus, promotes attachment. Filopodia provide cellular anchoring support and when prevalent, make cells more angular in shape. The median aspect ratio (length / width) of cells was found to be 1.38 on polished and 2.36 on NaOH-etched titanium. This, in addition to lower mean circularity shape factor values of 0.26 ± 0.03 on polished and 0.11 ± 0.01 on NaOH-etched titanium imply that the nanotextured surface promotes growth of cells more anchored to the substrate. This is also confirmed by increased perimeters of cells found on the NaOH-etched surface (950.92 ± 84.88 μm) compared with perimeter lengths of cells on the polished surface (668.55 ± 22.55 μm). Lastly, lower real time cell migration speed of 9 ± 1.2 μm / hour also suggests improved attachment of cells on NaOH-etched titanium with values speeds on the polished surface being 65 ± 19 μm / hour.
Surendra Tewari, PhD (Committee Chair)
Joanne Belovich, PhD (Committee Member)
Ronald Midura, PhD (Committee Member)
145 p.

Recommended Citations

Citations

  • Jensen, R. L. (2013). Live Cell Imaging to Investigate Bone Marrow Stromal Cell Adhesion and Migration on Titanium Surfaces: A Micro-Incubator in vitro Model [Master's thesis, Cleveland State University]. OhioLINK Electronic Theses and Dissertations Center. http://rave.ohiolink.edu/etdc/view?acc_num=csu1391128419

    APA Style (7th edition)

  • Jensen, Rebecca. Live Cell Imaging to Investigate Bone Marrow Stromal Cell Adhesion and Migration on Titanium Surfaces: A Micro-Incubator in vitro Model. 2013. Cleveland State University, Master's thesis. OhioLINK Electronic Theses and Dissertations Center, http://rave.ohiolink.edu/etdc/view?acc_num=csu1391128419.

    MLA Style (8th edition)

  • Jensen, Rebecca. "Live Cell Imaging to Investigate Bone Marrow Stromal Cell Adhesion and Migration on Titanium Surfaces: A Micro-Incubator in vitro Model." Master's thesis, Cleveland State University, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=csu1391128419

    Chicago Manual of Style (17th edition)