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Instructions

Student presentations must have a faculty sponsor.

Abstracts must include a title and a description of the research, scholarship, or creative work. The description should be 150-225 words in length and constructed in a format or style appropriate for the presenter’s discipline.

The following points should be addressed within the selected format or style for the abstract:

  • A clear statement of the problem or question you pursued, or the scholarly goal or creative theme achieved in your work.
  • A brief comment about the significance or uniqueness of the work.
  • A clear description of the methods used to achieve the purpose or goals for the work.
  • A statement of the conclusions, results, outcomes, or recommendations, or if the work is still in progress, the results you expect to report at the event.

Presenter photographs should be head and shoulder shots comparable to passport photos.

Additional Information

More information is available at carthage.edu/celebration-scholars/. The following are members of the Research, Scholarship, and Creativity Committee who are eager to listen to ideas and answer questions:

  • Jun Wang
  • Kim Instenes
  • John Kirk
  • Nora Nickels
  • Andrew Pustina
  • James Ripley

THE EFFECTS OF POTASSIUM CHLORIDE ON REACTIVE ASTROCYTOSIS IN AXON GROWTH PERMISSIVE AND INHIBITORY ASTROCYTE CELL LINES

Name: Victoria Lumbert
Major: Neruoscience and Biology
Hometown: Oswego, IL
Faculty Sponsor:
Other Sponsors:  
Type of research: Independent research

Name: Leslie Krause
Major: Neuroscience and Psychology
Hometown: Kenosha, WI
Faculty Sponsor:
Other Sponsors:  
Type of research: Independent research

Name: Allison Rendon
Major: Neuroscience and Psychology
Hometown: Chicago, IL
Faculty Sponsor:
Other Sponsors:  
Type of research: Independent research

Abstract

In response to central nervous system (CNS) injury such as a stroke, astrocytes undergo a series of cellular and molecular changes referred to as reactive astrocytosis. These changes range from mild to severe hypertrophy, proliferation, and upregulation of glial fibrillary acid protein (GFAP) expression, and may be modeled in cell culture by disrupting potassium homeostasis. The role of reactive astrocytosis in CNS injury remains debatable, with previous research suggesting that it may have beneficial effects, such as sequestering inflammation, and detrimental effects, such as inhibiting axon regeneration. To further our understanding of reactive astrocytosis, our studies characterize this process in two complementary CNS astrocyte cell lines: A7 cells, which are axon growth permissive, and Neu7 cells, which are axon growth inhibitory. Consistent with the role of reactive astrocytosis in inhibiting axon regeneration, we hypothesized that inhibitory Neu7 cells would be reactive under standard culture conditions and less susceptible to astrocytosis induced by increased extracellular potassium chloride. Conversely, we hypothesized that permissive A7 cells would be more susceptible to potassium chloride. Our results suggest that exposure to potassium chloride produces time- and dose-dependent increases in hypertrophy, proliferation, and GFAP expression in A7 and Neu7 cells. Continued characterization of reactive astrocytosis in A7 and Neu7 cells may provide unique models for defining the role of astrocytes in CNS injury, including elucidation of novel therapeutic targets for stroke.

Poster file

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