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Amelia K. Linnemann, PhD
Associate Professor of Pediatrics
Adjunct Associate Professor of Anatomy, Cell Biology & Physiology
Adjunct Associate Professor of Biochemistry & Molecular Biology
- Phone
- (317) 274-1568
- Address
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16 Tech Bldg 1, 4103 C
PENB
IN
Indianapolis, IN - PubMed:
-
Bio
Dr. Amelia Linnemann received her Bachelor of Science in Biology from the University of Detroit Mercy and her PhD in Molecular Biology and Genetics from Wayne State University. She then completed postdoctoral training at the University of Wisconsin-Madison. Dr. Linnemann is now an Associate Professor (with tenure) in the Department of Pediatrics at Indiana University School of Medicine in Indianapolis, IN. She is a member of both the Herman B Wells Center for Pediatric Research and the National Institutes of Health-funded Indiana Center for Diabetes and Metabolic Diseases (CDMD). She is also the director of the CDMD Microscopy Core and the Associate Director of Pipeline Program Development at IU School of Medicine.
Dr. Linnemann is the prior recipient of a prestigious K01 Career Development Award from the National Institutes of Health, has maintained continuous extramural funding since establishing her lab in 2016, and is a member of the NIDDK-Human Islet Research Network (HIRN). Research in Dr. Linnemann’s laboratory is focused on the study of the insulin-producing pancreatic beta-cells under conditions of inflammatory stress. Dr. Linnemann is particularly interested in how higher-level metabolic signals contribute to molecular crosstalk within the islet and influence beta-cell adaptation to stress, specifically through studies focused on autophagy and the antioxidant response. Her team uses cutting-edge imaging approaches to study these pathways and has developed a series of novel tools for use with intravital microscopy. Her lab was the first group to demonstrate defective autophagy in human type 1 diabetes, and their observations suggested lysosomal dysfunction prior to diabetes onset in autoantibody positive individuals. Thus, many of the current studies in the lab are focused on biological processes in early diabetes development, as well as developing and optimizing tools for in vivo imaging of pancreatic islet function associated with diabetes pathogenesis.
Year | Degree | Institution |
---|---|---|
2012 | Postdoctoral Training | University of Wisconsin School of Medicine and Public Health |
2009 | PhD | Wayne State University |
2002 | BS | University of Detroit Mercy |
Research in the Linnemann lab is focused on diabetes; specifically the study of the insulin producing pancreatic beta-cells under conditions of inflammatory stress. The beta-cells must adapt rapidly to changing conditions in the body in order to maintain blood glucose within a normal range. When pancreatic islets are exposed to additional stress and demand due to factors such as inflammation or obesity, some beta-cells are better able to adapt and respond in such a way that allows them to survive. An inability to adapt contributes significantly to the development of diabetes. Thus, we are particularly interested in how higher level metabolic signals contribute to molecular crosstalk within the islet and influence beta-cell adaptation to stress. In an effort to develop therapies that prevent beta-cell failure in type 1 and type 2 diabetes, projects in the lab are focused on 3 major areas:
- Identifying mechanisms of adaptive stress response in the pancreatic islet that enable beta-cell survival.
- Studying paracrine signaling in the islet under conditions of stress and increased demand.
- Understanding the regulation of core mediators of autophagy and how this process contributes to beta-cell homeostasis and survivial.
Desc: Trustee Teaching Award
Scope: University
Date: 2020-05-01