DIABETES & PANCREATITIS Role of the SIK2-p35-PJA2 Complex in Pancreatic ß-Cell Functional Compensation Researchers delineate a complex consisting of the AMP-activated protein kinase-related kinase SIK2, the CDK5 activator CDK5R1 and the E3 ligase PJA2 essential for ß-cell functional compensation. [Nat Cell Biol] Abstract Islet Microenvironment, Modulated by Vascular Endothelial Growth Factor-A Signaling, Promotes ß Cell Regeneration Researchers transiently increased vascular endothelial growth factor-A (VEGF-A) production by ß cells. VEGF-A induction dramatically increased the number of intra-islet endothelial cell but led to ß cell loss. [Cell Metab] Abstract | Graphical Abstract Syntaxin 4 Upregulation Increases Efficiency of Insulin Release in Pancreatic Islets from Humans with and without Type 2 Diabetes Mellitus Human islets from type 2 diabetic and healthy individuals transduced to over-express Syntaxin 4 were examined by perifusion analysis. Streptozotocin-induced diabetic recipient mice transplanted with Syntaxin 4-enriched or normal islets were assessed for rescue of diabetes in vivo. [J Clin Endocrinol Metab] Abstract IGF-I Stimulates CCN5/WISP2 Gene Expression in Pancreatic ß-Cells, which Promotes Cell Proliferation and Survival against Streptozotocin To define the role of CCN5 in islet cell biology, scientists stably overexpressed its cDNA in insulinoma MIN6 cells and detected a two-fold increase in the proliferation of MIN6-CCN5 compared to control cells that correlated with significant elevations in the levels of cyclin D1 and the phosphorylation of Akt and Erk2. [Endocrinology] Abstract High Oxygen Condition Facilitates the Differentiation of Mouse and Human Pluripotent Stem Cells into Pancreatic Progenitors and Insulin-Producing Cells Researchers tried to establish an effective method for the differentiation of induced pluripotent stem cells into insulin-producing cells by culturing under high oxygen (O2) conditions. They found that a high O2 condition repressed Notch-dependent gene Hes1 expression and increased Ngn3 expression at the stage of pancreatic progenitors. [J Biol Chem] Abstract | Full Article Calcium Co-Regulates Oxidative Metabolism and ATP-Synthase Dependent Respiration in Pancreatic Beta-Cells Investigators have studied glucose-induced calcium signaling and energy metabolism, in INS-1E insulinoma cells and human islet beta-cells. [J Biol Chem] Abstract | Full Article Silencing of the Fibroblast Growth Factor 21 Gene Is an Underlying Cause of Acinar Cell Injury in Mice Lacking MIST1 Researchers examined the regulation and function of fibroblast growth factor 21 in acinar cell injury, specifically in a mouse model of pancreatic injury (Mist1-/-). Mist1-/- mice exhibit acinar cell disorganization, decreased acinar cell communication and exocytosis, and increased sensitivity to cerulein-induced pancreatitis. [Am J Physiol Endocrinol Metab] Abstract PANCREATIC CANCER Analysis of the Tumor-Initiating and Metastatic Capacity of PDX1-Positive Cells from the Adult Pancreas Scientists sought to determine which subsets of pancreatic and duodenal homeobox 1 (PDX1)+ cells may be responsible for tumor growth. Using the Lox-Stop-Lox-KrasG12D genetic mouse model of pancreatic carcinogenesis, they isolated a population of KrasG12D-expressing PDX1+ cells with an inherent capacity to metastasize. [Proc Natl Acad Sci USA] Abstract Transcriptional Regulation of Fibronectin by p21-Activated Kinase-1 Modulates Pancreatic Tumorigenesis Scientists analyzed the expression of p21-activated kinase 1 in human pancreatic cancer tissues and found that Pak1 levels are significantly upregulated in pancreatic ductal adenocarcinoma samples as compared with adjacent normals. [Oncogene] Abstract Anticancer Effects of Gemcitabine Are Enhanced by Co-Administered iRGD Peptide in Murine Pancreatic Cancer Models that Overexpressed Neuropilin-1 Researchers identified a subset of pancreatic cancer models that showed neuropilin-1 overexpression sensitive to internalized-RGD (iRGD) co-administration. [Br J Cancer] Abstract LSD1 Sustains Pancreatic Cancer Growth via Maintaining HIF1a-Dependent Glycolytic Process Using in vitro and in vivo models, researchers demonstrated that knock-down of lysine specific demethylase 1 (LSD1) repressed proliferation and tumorigenicity of pancreatic cancer cells. [Cancer Lett] Abstract |