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The Yi laboratory is interested in the research of pancreatic beta cells in Type 1 and Type 2 diabetes. The laboratory uses a multidisciplinary approach to study pancreatic beta cell regeneration, function, stress and protection against autoimmune destruction in Type 1 Diabetes. Our goal is to discover and study novel therapeutic targets and improve the treatment of both Type 1 and Type 2 diabetes.

 Dr. Peng Yi is originally from Shandong, China, graduated from the University of Science and Technology of China. He was trained by Dr. Eric Olson and received his Ph.D. degree in UT Southwestern Medical Center. He then worked in Dr. Doug Melton’s lab in Harvard University as a postdoc fellow. In 2013, Dr. Yi become an Assistant Investigator in Joslin Diabetes Center. Currently, he is also the director of Joslin Diabetes Center CRISPR screen core laboratory.

  1. The mechanism of pancreatic beta cell replication.

 We are interested in studying gene networks and signaling pathways that control pancreatic beta cell replication under insulin resistance. The laboratory set up an acute insulin resistance mouse model by infusion of an insulin receptor antagonist, S961, which induces dramatic and specific pancreatic beta-cell replication. Our major focus is using this model to search for novel factors, secreted proteins and hormones from various organs/tissues, as well as beta-cell genes that control pancreatic beta-cell proliferation. We also use this model to study cross-organ communication that regulates beta cell functions.

  1. The mechanism of pancreatic beta cell neogenesis from pancreatic duct cells.

 Pancreatic beta cells can be trans-differentiated from other cell types, such as pancreatic duct cells (beta cell neogenesis from duct cells). Many evidences suggest that pancreatic duct cells have the potential to serve as beta cell progenitor cells under certain conditions, but the underlying mechanism is poorly understood. Our laboratory uses genome-wide CRISPR screen trying to identify novel genes and signal pathways that control the trans-differentiation of pancreatic duct cells into beta or beta-like cells.

  1. Genetic protection of pancreatic beta-cells against autoimmune destruction in Type 1 Diabetes.

 The laboratory is using whole-genome gain-of-function and loss-of-function in vivo CRISPR screens to investigate the mechanism of pancreatic beta-cell tolerance and vulnerability in Type 1 Diabetes. We recently discovered 11 novel genes, the mutation of which can render beta-cells resistant to autoimmune killing.  We currently focus on the study of one of these genes, RNLS, a Type 1 Diabetes GWAS gene. We also identified an FDA approved drug, pargyline, that is able to target RNLS and protect pancreatic beta cells in Type 1 Diabetes mouse model.

  1. Genome-wide CRISPR screens to study various questions in beta cell biology.

 The laboratory is applying a genome-wide CRISPR screen technique to investigate various questions in beta cell biology, including beta-cell stress, function, allotransplantation tolerance, as well as human beta-cell proliferation.

Contact Information

Office Phone

(617) 309-2627

peng.yi [at] joslin.harvard.edu

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Protecting beta cells against stress may guard against type 1 diabetes

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