Date Approved

11-2015

Degree Type

Open Access Thesis

Degree Name

Master of Science (MS)

Department

Biology

Committee Member

Dr. Robert Winning, Ph.D., Chair

Committee Member

Dr. Linda Samuelson, Ph.D., Project Supervisor

Committee Member

Dr. Anne Casper, Ph.D.

Committee Member

Dr. Glenn Walker, Ph.D.

Abstract

Very few genetic markers for gastric stem cells are currently described. Identifying new markers is important for increasing our basic understanding of gastric tissues and studying mechanisms of cancer development. Gastric and intestinal tissues share a common developmental program. Thus, intestinal stem cell genetic drivers were investigated for putative expression in gastric stem cells, utilizing Cre/Lox technology for lineage tracing. The recombination efficiencies of reporters with intestinal drivers and the effect of tamoxifen-induced tissue damage were also investigated.

It was discovered that higher doses of tamoxifen do not increase reporter activation in the intestine but induce gastric tissue damage. It was also determined that Bmil1and Lrig1 are markers for stem cells throughout the glandular stomach. Thus, two new gastric stem cell drivers have been identified that will be useful for genetic manipulation of gastric epithelium.

Included in

Biology Commons

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