Agata Jurczyk PhD
|Institution||University of Massachusetts Medical School|
|Department||Program in Molecular Medicine|
|Address||University of Massachusetts Medical School|
368 Plantation Street, AS7-2046
Worcester MA 01605
- Elms College, Chicopee Massachusetts - B.A. in Bio/Chem/Math Magna Cum Laude
- Smith College, Northampton, Massachusetts - M.A. in Plant Biology
- University of Massachusetts Medical School, Worcester, Massachusetts - Ph.D. in Cell Biology
My research is focused on mechanisms of insulin secretion in pancreatic beta cells. I am a cell biologist with expertise inmicroscopy and image analysis, molecular biology and cellular biology. Recently, I have uncovered an unexpected rolefor the centrosomal protein pericentrin in maintaining normal insulin storageand secretion. This research led me to discover a link between centrosomeproteins and diabetes. I am currently trying to understand the molecular mechanism(s)behind high prevalence of diabetes among patients with centrosome and ciliadefects.
It is known that patients with centrosomeand cilia defects have an elevated risk of developing diabetes, yet themolecular mechanisms underlying this association are not understood. Thecentrosome protein DISC1 (Disrupted in Schizophrenia 1) is a centrosome proteinthat also localizes to primary cilia and it is mutated in schizophrenicpatients who also have elevated predisposition to diabetes. The importance of DISC1in brain development and function is well recognized; however, nothing is knownabout its role in pancreatic beta cells, where it is also highly expressed.Since DISC1 is a direct interacting protein of pericentrin, and we have alreadyshown the importance of pericentrin for insulin secretion, I hypothesized thatdefects in DISC1 function or regulation in pancreatic beta cells may contributeto the development of diabetes. We anticipate that our studies will reveal thenormal function of DISC1 in pancreatic beta cells as well as provide insightsinto the high concordance of diabetes in schizophrenic patients.
Bardet-Biedl Syndrome (BBS) is a pleiotropicciliopathy characterized by a unique phenotype including obesity, type II diabetesand neurological impairments. The specific link between BBS and the developmentof type II diabetes among BBS patients is not currently understood. My researchexamines how loss of the Bardet-Biedl Syndrome 2 gene affects the function of pancreaticislets. The role of ciliary proteins in pancreatic islets will provide newinsights into the pathogenesis of diabetes and reveal potential new therapy fortreatments.
For assistance with using Profiles, please refer to the online tutorials
or contact UMMS Help Desk
or call 508-856-8643.
Click the "See All" links for more information and interactive visualizations!
People who are also in this person's primary department.