User menu

Dynamics and Regulation of Insulin Secretion in Pancreatic Islets from Normal Young Children.

Bibliographic reference Henquin, Jean-Claude ; Nenquin, Myriam. Dynamics and Regulation of Insulin Secretion in Pancreatic Islets from Normal Young Children.. In: PLoS One, Vol. 11, no.11, p. e0165961 (2016)
Permanent URL
  1. Thomas P., Cote G., Wohllk N, Haddad B, Mathew P., Rabl W, Aguilar-Bryan L, Gagel R., Bryan J, Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy, 10.1126/science.7716548
  2. DUNNE M. J., Hyperinsulinism in Infancy: From Basic Science to Clinical Disease, 10.1152/physrev.00022.2003
  3. Stanley Charles A., Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders, 10.1210/jc.2015-3651
  4. Hattersley A. T., Ashcroft F. M., Activating Mutations in Kir6.2 and Neonatal Diabetes: New Clinical Syndromes, New Scientific Insights, and New Therapy, 10.2337/diabetes.54.9.2503
  5. Babenko Andrey P., Polak Michel, Cavé Hélène, Busiah Kanetee, Czernichow Paul, Scharfmann Raphael, Bryan Joseph, Aguilar-Bryan Lydia, Vaxillaire Martine, Froguel Philippe, Activating Mutations in theABCC8Gene in Neonatal Diabetes Mellitus, 10.1056/nejmoa055068
  6. P. Keskinen, S. Korhonen, A. Kupila, R. Veijola, S. Erkkilä, H. Savolainen, P. Arvilommi, T. Simell, J. Ilonen, M. Knip, O. Simell, First-phase insulin response in young healthy children at genetic and immunological risk for Type I diabetes, 10.1007/s00125-002-0981-8
  7. Rahier J., Wallon J., Henquin J.C., Cell populations in the endocrine pancreas of human neonates and infants, 10.1007/bf00252762
  8. Wirdnam P.K., Milner R.D.G., Quantitation of the B and A cell fractions in human pancreas from early fetal life to puberty, 10.1016/0378-3782(81)90037-2
  9. Stefan Y., Grasso S., Perrelet A., Orci L., A Quantitative Immunofluorescent Study of the Endocrine Cell Populations in the Developing Human Pancreas, 10.2337/diab.32.4.293
  10. Meier J. J., Butler A. E., Saisho Y., Monchamp T., Galasso R., Bhushan A., Rizza R. A., Butler P. C.,  -Cell Replication Is the Primary Mechanism Subserving the Postnatal Expansion of  -Cell Mass in Humans, 10.2337/db07-1369
  11. Gregg Brigid E., Moore Patrick C., Demozay Damien, Hall Ben A., Li Mei, Husain Aliya, Wright Amy J., Atkinson Mark A., Rhodes Christopher J., Formation of a Human β-Cell Population within Pancreatic Islets Is Set Early in Life, 10.1210/jc.2012-1206
  12. Hawdon J M, Aynsley-Green A, Alberti K G, Ward Platt M P, The role of pancreatic insulin secretion in neonatal glucoregulation. I. Healthy term and preterm infants., 10.1136/adc.68.3_spec_no.274
  13. Stumpp Christian, Beyerlein Andreas, Ziegler Anette-Gabriele, Bonifacio Ezio, Neonatal and infant beta cell hormone concentrations in relation to type 1 diabetes risk : Beta-cell hormones and autoimmunity, 10.1111/pedi.12122
  14. REITANO G., GRASSO S., DISTEFANO G., MESSINA A., The Serum Insulin and Growth Hormone Response to Arginine and to Arginine with Glucose in the Premature Infant, 10.1210/jcem-33-6-924
  15. Grasso S., Messina A., Distefano G., Vigo R., Reitano G., Insulin Secretion in the Premature Infant: Response to Glucose and Amino Acids, 10.2337/diab.22.5.349
  16. Falorni A., Fracassini F., Massi-Benedetti F., Maffei S., Glucose Metabolism and Insulin Secretion in the Newborn Infant: Comparisons Between the Responses Observed the First and Seventh Day of Life to Intravenous and Oral Glucose Tolerance Tests, 10.2337/diab.23.3.172
  17. Mericq V., Ong K. K., Bazaes R., Peña V., Avila A., Salazar T., Soto N., Iñiguez G., Dunger D. B., Longitudinal changes in insulin sensitivity and secretion from birth to age three years in small- and appropriate-for-gestational-age children, 10.1007/s00125-005-0036-z
  18. Robert J.-J., Deschamps I., Chevenne D., Roger M., Mogenet A., Boitard C., Relationship Between First-Phase Insulin Secretion and Age, HLA, Islet Cell Antibody Status, and Development of Type I Diabetes in 220 Juvenile First-Degree Relatives of Diabetic Patients, 10.2337/diacare.14.8.718
  19. Carel J C, Boitard C, Bougnères P F, Decreased insulin response to glucose in islet cell antibody-negative siblings of type 1 diabetic children., 10.1172/jci116595
  20. Caprio Sonia, Plewe Gerd, Diamond Michael P., Simonson Donald C., Boulware Susan D., Sherwin Robert S., Tamborlane William V., Increased insulin secretion in puberty: A compensatory response to reductions in insulin sensitivity, 10.1016/s0022-3476(89)80438-x
  21. Chase H.Peter, Cuthbertson David D., Dolan Lawrence M., Kaufman Francine, Krischer Jeffrey P., Schatz Desmond A., White Neil H., Wilson Darrell M., Wolfsdorf Joseph, First-phase insulin release during the intravenous glucose tolerance test as a risk factor for type 1 diabetes, 10.1067/mpd.2001.111274
  22. S Arslanian, J Clin Endocrinol Metab, 82, 1923 (1997)
  24. Agren A., Andersson A., Bjorken C., Groth C. G., Gunnarsson R., Hellerstrom C., Lindmark G., Lundqvist G., Petersson B., Swenne I., Culture and Function in Vitro, 10.2337/diab.29.1.s64
  25. H Jahr, Diabetes Metab, 7, 71 (1981)
  26. Hoffman L., Mandel T.E., Carter W.M., Koulmanda M., Martin F.I.R., Insulin secretion by fetal human pancreas in organ culture, 10.1007/bf00260956
  27. Otonkoski T, Hayek A, Constitution of a biphasic insulin response to glucose in human fetal pancreatic beta-cells with glucagon-like peptide 1., 10.1210/jcem.80.12.8530635
  28. J Tu, J Clin Endocrinol Metab, 82, 943 (1997)
  29. Otonkoski T., Andersson S., Knip M., Simell O., Maturation of Insulin Response to Glucose During Human Fetal and Neonatal Development: Studies with Perifusion of Pancreatic Isletlike Cell Clusters, 10.2337/diab.37.3.286
  30. Balamurugan A. N., Chang Y., Bertera S., Sands A., Shankar V., Trucco M., Bottino R., Suitability of human juvenile pancreatic islets for clinical use, 10.1007/s00125-006-0318-0
  31. Henquin Jean-Claude, Nenquin Myriam, Sempoux Christine, Guiot Yves, Bellanné-Chantelot Christine, Otonkoski Timo, de Lonlay Pascale, Nihoul-Fékété Claire, Rahier Jacques, In vitro insulin secretion by pancreatic tissue from infants with diazoxide-resistant congenital hyperinsulinism deviates from model predictions, 10.1172/jci58400
  32. Fox Jocelyn E. Manning, Seeberger Karen, Dai Xiao Qing, Lyon James, Spigelman Aliya F., Kolic Jelena, Hajmrle Catherine, Joseph Jamie W., Kin Tatsuya, Shapiro A.M. James, Korbutt Gregory, MacDonald Patrick E., Functional Plasticity of the Human Infant β-Cell Exocytotic Phenotype, 10.1210/en.2012-1934
  33. Henquin J.-C., Dufrane D., Nenquin M., Nutrient Control of Insulin Secretion in Isolated Normal Human Islets, 10.2337/db06-0868
  34. Henquin Jean-Claude, Dufrane Denis, Kerr-Conte Julie, Nenquin Myriam, Dynamics of glucose-induced insulin secretion in normal human islets, 10.1152/ajpendo.00251.2015
  35. Detimary P, Jonas J C, Henquin J C, Stable and diffusible pools of nucleotides in pancreatic islet cells., 10.1210/endo.137.11.8895332
  36. Ishiyama N., Dual mechanism of the potentiation by glucose of insulin secretion induced by arginine and tolbutamide in mouse islets, 10.1152/ajpendo.00032.2005
  37. Sato Yoshihiko, Anello Marcello, Henquin Jean-Claude, Glucose Regulation of Insulin Secretion Independent of the Opening or Closure of Adenosine Triphosphate-Sensitive K+Channels in β Cells1, 10.1210/endo.140.5.6729
  38. C Sempoux, Mod Pathol, 11, 444 (1998)
  39. Kassem S. A., Ariel I., Thornton P. S., Scheimberg I., Glaser B., Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy, 10.2337/diabetes.49.8.1325
  40. R Jaffe, Perspect Pediatr Pathol, 7, 137 (1982)
  41. Atiya A, Intraislet somatostatin inhibits insulin (via a subtype-2 somatostatin receptor) but not islet amyloid polypeptide secretion in the isolated perfused human pancreas,, 10.1016/s1091-255x(97)80117-5
  42. Hauge-Evans A. C., King A. J., Carmignac D., Richardson C. C., Robinson I. C.A.F., Low M. J., Christie M. R., Persaud S. J., Jones P. M., Somatostatin Secreted by Islet  -Cells Fulfills Multiple Roles as a Paracrine Regulator of Islet Function, 10.2337/db08-0792
  43. CC Richardson, Diabetologia, 50, 1000 (2007)
  44. Henquin J.-C., Sempoux C., Marchandise J., Godecharles S., Guiot Y., Nenquin M., Rahier J., Congenital Hyperinsulinism Caused by Hexokinase I Expression or Glucokinase-Activating Mutation in a Subset of  -Cells, 10.2337/db12-1414
  45. Stolovich-Rain Miri, Enk Jonatan, Vikesa Jonas, Nielsen Finn Cilius, Saada Ann, Glaser Benjamin, Dor Yuval, Weaning Triggers a Maturation Step of Pancreatic β Cells, 10.1016/j.devcel.2015.01.002
  46. Dhawan Sangeeta, Tschen Shuen-Ing, Zeng Chun, Guo Tingxia, Hebrok Matthias, Matveyenko Aleksey, Bhushan Anil, DNA methylation directs functional maturation of pancreatic β cells, 10.1172/jci79956
  47. Jacovetti Cécile, Matkovich Scot J., Rodriguez-Trejo Adriana, Guay Claudiane, Regazzi Romano, Postnatal β-cell maturation is associated with islet-specific microRNA changes induced by nutrient shifts at weaning, 10.1038/ncomms9084