Defining Alpha and Beta-Cell Crosstalk for the Treatment and Prevention of Diabetes

Abstract

During this funding period we have bred up mice for study, have begun to enroll mice into study and generate samples for analysis in both aims 1 and 2. The primary finding to report at this time is our work in sham and VSG-operated MIPCre+ and MIPCre- mice that do not contain the floxed GLP-1R allele. These additional control groups demonstrate that the MIPCre allele does not alter our glucoregulatory findings after VSG in mice. In addition, as a complementary approach, we have developed a new single cell RNA-sequencing method for the study of islets. We have used this approach to study islets treated with and without a GLP-1 receptor agonist from healthy human donors. These data reveal that GLP-1 receptor signaling in human islets increases alpha cell expression of the prohormone convertase needed for GLP-1 production, demonstrating that our model of beta cell GLP-1R function has translational relevance in humans.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2019
Accession Number
AD1094164

Entities

People

  • Bethany P. Cummings

Organizations

  • Cornell University

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Acquisition
  • Bariatrics
  • Bile
  • Biomedical Research
  • Body Weight
  • Breeding
  • Co-Channel Interference
  • Culture Media
  • Culture Techniques
  • Diabetes
  • Diabetes Mellitus
  • Digestive System Processes
  • Hormones
  • Medical Personnel
  • Rna Sequence Analysis
  • Students
  • Type 2 Diabetes

Fields of Study

  • Biology

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