Abstract
Islet transplantation can cure type 1 diabetes, but peri-transplant beta cell death limits this procedure to those with low insulin requirements. Improving human beta cell survival or proliferation may make islet transplantation a possibility for more type 1 patients. To identify novel regulators of beta cell survival and proliferation, we conducted a pooled small hairpin RNA (shRNA) screen in primary human beta cells transplanted into immunocompromised mice. shRNAs targeting several cyclin dependent kinase inhibitors were enriched after transplant. Here, we focused on the Gi/o-coupled GPCR, serotonin 1F receptor ( HTR1F, 5-HT (1F) ) which our screen identified as a negative regulator of beta cell numbers after transplant. In vitro , 5-HT (1F) knockdown induced human beta cell proliferation but only when combined with harmine and exendin-4. In vivo , knockdown of 5-HT (1F) reduced beta cell death during transplant. To demonstrate the feasibility of targeting 5-HT (1F) in islet transplant, we identified and validated a small molecule 5-HT (1F) antagonist. This antagonist increased glucose stimulated insulin secretion from primary human islets and cAMP accumulation in primary human beta cells. Finally, the 5-HT (1F) antagonist improved glycemia in marginal mass, human islet transplants into immunocompromised mice. We identify 5-HT (1F) as a novel druggable target to improve human beta cell survival in the setting of islet transplantation. ONE SENTENCE SUMMARY: Serotonin 1F receptor (5-HT (1F) ) negatively regulates insulin secretion and beta cell survival during transplant.