College

Buchtel College of Arts and Sciences

Date of Last Revision

2025-04-29 12:38:47

Major

Biomedical Science

Honors Course

BIOL

Number of Credits

5

Degree Name

Bachelor of Science

Date of Expected Graduation

Spring 2025

Abstract

Among glial cells, astrocytes have a prevalent influence on supporting neuronal function and overall brain health. Specifically targeting this cell type for disease treatment is an existing issue. Other cell types tend to express the desired treatment, which is not always wanted and can lead to unintended, negative consequences. Astrocytes contribute largely to maintaining the blood brain barrier, which is disrupted in Parkinson’s disease. Certain genes are thought to be the reason for this disruption, so if they can be specifically targeted in astrocytes with a specific enhancer, the disruption of the disease could be reversed. In our experiment, we will use Golden-Gate cloning to insert separate enhancer genes, Slc28 and Stom2, into a plasmid with a DL5 reporter gene. In our analysis of specificity results, SOX9 will be used to identify the nuclei of the astrocytes and DAPI will be used to identify all nuclei present in that tissue sample. Specifically, the cortex and striatum will be the brain regions of interest. Our results will show that Slc28 was not evident to be astrocyte specific in either brain region; Stom2 is relatively astrocyte specific in the striatum’s astrocytes but not for the cortex. The result of the research will be whether the enhancers of interest would be beneficial in potential future treatment options that involve astrocyte gene expression. We suspect that by enhancing expression in certain cell types in the nervous system, potential treatments for neurodegenerative disorders can be utilized.

Research Sponsor

Dr. Brian Bagatto

First Reader

Andreas Pfenning

Second Reader

Zhexi Li

Honors Faculty Advisor

Brian Bagatto

Proprietary and/or Confidential Information

No

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