Skip to main content

Advertisement

Log in

Impact of Sur1 gene inactivation on the morphology of mouse pancreatic endocrine tissue

  • Regular Article
  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Abstract

In congenital hyperinsulinism of infancy (CHI), the loss of K-ATP channels (composed of Kir6.2 and SUR1 subunits) in β cells induces permanent insulin secretion and severe hypoglycaemia. By contrast, Sur1 −/− mice do not present such defects. We have investigated the impact of Sur1 gene inactivation on mouse islet cell morphology, structure and basic physiology. Pancreata were collected from young, adult and old wild-type (WT) and Sur1 −/− mice. After immunostaining for hormone, the total endocrine tissue, cell proportion, cell size and intra-insular distribution, hormone content and Glut-2 expression were quantified by morphometry. Basic physiological parameters were also measured. In young Sur1 −/− mice, the total endocrine tissue and proportion of β cells were higher (P<0.05) than in WT mice, whereas the proportion of δ cells was lower (P<0.01). In old Sur1 −/− mice, α cells were frequently located in the central regions of islets (unlike WT islets) and their proportion was increased (P<0.05). Glut-2 protein and mRNA levels were lower in old Sur1 −/− islets (P<0.02). Insulinaemia, fasting insulin and glucagon contents were equivalent in both groups of pancreata. Thus, the islets of Sur1 −/− mice present morphological modifications that have not been described in CHI and that might reflect an adaptive mechanism controlling insulin secretion in these mice.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Aguilar-Bryan L, Nichols CG, Wechsler SW, Clement JP 4th, Boyd AE 3rd, González G, Herrera-Sosa H, Nguy K, Bryan J, Nelson DA (1995) Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion. Science 268:423–426

    Article  PubMed  CAS  Google Scholar 

  • Ashcroft FM, Gribble FM (1998) Correlating structure and function in ATP-sensitive K+ channels. Trends Neurosci 21:288–294

    Article  PubMed  CAS  Google Scholar 

  • Bokvist K, Olsen HL, Hoy M, Gotfredsen CF, Holmes WF, Buschard K, Rorsman P, Gromada J (1999) Characterisation of sulphonylurea and ATP-regulated K+ channels in rat pancreatic A-cells. Pflügers Arch Eur J Physiol 438:428–436

    Article  CAS  Google Scholar 

  • Bosco D, Orci L, Meda P (1989) Homologous but not heterologous contact increases the insulin secretion of individual pancreatic beta-cells. Exp Cell Res 184:72–80

    Article  PubMed  CAS  Google Scholar 

  • Bouwens L, Rooman I (2005) Regulation of pancreatic beta-cell mass. Physiol Rev 85:1255–1270

    Article  PubMed  CAS  Google Scholar 

  • Brereton HC, Carvell MJ, Asare-Anane H, Graham R, Michael RC, Shanta JP, Peter MJ (2006) Homotypic cell contact enhances insulin but not glucagon secretion. Biochem Biophys Res Commun 344:995–1000

    Article  PubMed  CAS  Google Scholar 

  • Brissova M, Fowler MJ, Nicholson WE, Chu A, Hirshberg B, Harlan DM, Powers AC (2005) Assessment of human pancreatic islet architecture and composition by laser scanning confocal microscopy. J Histochem Cytochem 53:1087–1097

    Article  PubMed  CAS  Google Scholar 

  • Cabrera O, Berman DM, Kenyon NS, Ricordi C, Berggren PO, Caicedo A (2006) The unique cytoarchitecture of human pancreatic islets has implications for islet cell function. Proc Natl Acad Sci USA 103:2334–2339

    Article  PubMed  CAS  Google Scholar 

  • Detimary P, Jonas JC, Henquin JC (1996) Stable and diffusible pools of nucleotides in pancreatic islet cells. Endocrinology 137:4671–4676

    Article  PubMed  CAS  Google Scholar 

  • Dunne MJ, Kane C, Shepherd RM, Sanchez JA, James RF, Johnson PR, Aynsley-Green A, Lu S, Clement J, Lindley KJ, Seino S, Aguilar-Bryan L (1997) Familial persistent hyperinsulinaemic hypoglycaemia of infancy and mutations in the sulfonylurea receptor. N Engl Med 336:703–706

    Article  CAS  Google Scholar 

  • Esni F, Täljedal IB, Perl AK, Cremer H, Christofori G, Semb H (1999) Neural cell adhesion molecule (N-CAM) is required for cell type segregation and normal ultrastructure in pancreatic islets. J Cell Biol 144:325–337

    Article  PubMed  CAS  Google Scholar 

  • Falkmer S, Søvik O, Vidnes J (1981) Immunohistochemical, morphometric, and clinical studies of the pancreatic islets in infants with persistent neonatal hypoglycemia of familial type with hyperinsulinism and nesidioblastosis. Acta Biol Med Ger 40:39–54

    PubMed  CAS  Google Scholar 

  • Fournet JC, Junien C (2004) Genetics of congenital hyperinsulinism. Endocr Pathol 15:233–240

    Article  PubMed  Google Scholar 

  • Glaser B, Kesavan P, Heyman M, Davis E, Cuesta A, Buchs A, Stanley CA, Thornton PS, Permutt MA, Matschinsky FM, Herold KC (1998) Familial hyperinsulinism caused by an activating glucokinase mutation. N Engl J Med 338:226–230

    Article  PubMed  CAS  Google Scholar 

  • Goossens A, Gepts W, Saudubray JM, Bonnefont JP, Nihoul-Fékété C, Heitz PU, Klöppel G (1989) Diffuse and focal nesidioblastosis: a clinicipathological study of 24 patients with persistent neonatal hyperinsulinaemic hypoglycaemia. Am J Surg Pathol 13:766–775

    Article  PubMed  CAS  Google Scholar 

  • Göpel SO, Kanno T, Barg S, Rorsman P (2000) Patch-clamp characterisation of somatostatin-secreting δ-cells in intact mouse pancreatic islets. J Physiol (Lond) 528:497–507

    Article  Google Scholar 

  • Gromada J, Ma X, Hoy M, Bokvist K, Salehi A, Berggren PO, Rorsman P (2004) ATP-sensitive K+ channel-dependent regulation of glucagon release and electrical activity by glucose in wild-type and SUR1−/− mouse α-cells. Diabetes 53:S181–S189

    Article  PubMed  CAS  Google Scholar 

  • Guiot Y, Henquin JC, Rahier J (1994) Effects of glibenclamide on pancreatic beta-cell proliferation in vivo. Eur J Pharmacol 261:157–161

    Article  PubMed  CAS  Google Scholar 

  • Guiot Y, Stevens M, Marhfour I, Stiernet P, Mikhailov M, Ashcroft SJH, Rahier J, Henquin JC, Sempoux C (2007) Morphological localisation of sulfonylurea receptor 1 in endocrine cells of human, mouse and rat pancreas. Diabetologia 50:1889–1899

    Article  PubMed  CAS  Google Scholar 

  • Hamaguchi K, Utsunomiya N, Takaki R, Yoshimatsu H, Sakata T (2003) Cellular interaction between mouse pancreatic alpha-cell and beta-cell lines: possible contact-dependent inhibition of insulin secretion. Exp Biol Med 228:1227–1233

    CAS  Google Scholar 

  • Hauge-Evans AC, Squires PE, Persaud SJ, Jones PM (1999) Pancreatic beta-cell-to-beta-cell interactions are required for integrated responses to nutrient stimuli: enhanced Ca2+ and insulin secretory responses of MIN6 pseudoislets. Diabetes 48:1402–1408

    Article  PubMed  CAS  Google Scholar 

  • Henquin JC (2000) Triggering and amplifying pathways of regulation of insulin secretion by glucose. Diabetes 49:1751–1760

    Article  PubMed  CAS  Google Scholar 

  • Johnson JD, Ahmed NT, Luciani DS, Han Z, Tran H, Fujita J, Misler S, Edlund H, Polonsky KS (2003) Increased islet apoptosis in Pdx1+/− mice. J Clin Invest 111:1147–1160

    PubMed  CAS  Google Scholar 

  • Ku SK, Lee HS, Lee JH (2002) An immunohistochemical study on the pancreatic endocrine cells of the C57BL/6 mouse. J Vet Sci 3:327–333

    PubMed  Google Scholar 

  • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods 25:402–408

    Article  PubMed  CAS  Google Scholar 

  • Lonlay P de, Fournet JC, Rahier J, Gross-Morand MS, Poggi F, Foussier V, Bonnefont JP, Brusset MC, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C (1997) Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinaemic hypoglycaemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy. J Clin Invest 100:802–807

    Article  PubMed  Google Scholar 

  • MacDonald PE, De Marinis YZ, Ramracheya R, Salehi A, Ma X, Johnson PR, Cox R, Eliasson L, Rorsman P (2007) A K ATP channel-dependent pathway within alpha cells regulates glucagon release from both rodent and human islets of Langerhans. PLoS Biol 15:233–240

    Google Scholar 

  • Miki T, Tashiro F, Iwanaga T, Nagashima K, Yoshitomi H, Aihara H, Gonoi T, Inagaki N, Miyazaki J, Seino S (1997) Abnormalities of the pancreatic islets by targeted expression of a dominant-negative KATP channel. Proc Natl Acad Sci 94:11969–11973

    Article  PubMed  CAS  Google Scholar 

  • Miki T, Nagashima K, Tashiro F, Kotake K, Yoshitomi H, Tamamoto A, Gonoi T, Iwanaga T, Miyazaki J, Seino S (1998) Defective insulin secretion and enhanced insulin action in KATP channel-deficient mice. Proc Natl Acad Sci USA 95:10402–10406

    Article  PubMed  CAS  Google Scholar 

  • Nenquin M, Szollosi A, Aguillar-Bryan L, Bryan J, Henquin JC (2004) Both triggering and amplifying pathways contribute to fuel-induced insulin secretion in the absence of sulfonylurea receptor-1 in pancreatic beta-cells. J Biol Chem 279:32316–32324

    Article  PubMed  CAS  Google Scholar 

  • Norman M, Moldovan S, Seghers V, Wang XP, DeMayo FJ, Brunicardi FC (2002) Sulfonylurea receptor knockout causes glucose intolerance in mice that is not alleviated by concomitant somatostatin subtype receptor 5 knockout. Ann Surg 235:767–774

    Article  PubMed  Google Scholar 

  • Rahier J, Wallon J, Henquin JC (1981) Cell populations in the endocrine pancreas of human neonates and infants. Diabetologia 20:540–546

    Article  PubMed  CAS  Google Scholar 

  • Rahier J, Fält K, Müntefering H, Becker K, Gepts W, Falkmer S (1984) The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: deficiency of pancreatic D cells or hyperactivity of B cells? Diabetologia 26:282–289

    Article  PubMed  CAS  Google Scholar 

  • Rahier J, Stevens M, De Menten Y, Henquin JC (1989) Determination of antigen concentration in tissue sections by immunodensitometry. Lab Invest 61:357–363

    PubMed  CAS  Google Scholar 

  • Rahier J, Guiot Y, Sempoux C (2000) Persistent hyperinsulinaemic hypoglycaemia of infancy: a heterogeneous syndrome unrelated to nesidioblastosis. Arch Dis Child Fetal Neonatal Ed 82:F108–F112

    Article  PubMed  CAS  Google Scholar 

  • Seghers V, Nakazaki M, DeMayo F, Aguillar-Bryan L, Bryan J (2000) Sur1 knockout mice: a model for KATP channel-independent regulation of insulin secretion. J Biol Chem 275:9270–9277

    Article  PubMed  CAS  Google Scholar 

  • Seino S, Miki T (2003) Physiological and pathophysiological roles of ATP-sensitive K+ channels. Prog Biophys Mol Biol 81:133–176

    Article  PubMed  CAS  Google Scholar 

  • Seino S, Iwanaga T, Nagashima K, Miki T (2000) Diverse roles of KATP channels learned from Kir6.2 genetically engineered mice. Diabetes 49:311–318

    Article  PubMed  CAS  Google Scholar 

  • Sempoux C, Guiot Y, Lefèvre A, Nihoul-Fékété C, Jaubert F, Saudubray JM, Rahier J (1998) Neonatal hyperinsulinaemic hypoglycaemia: heterogeneity of the syndrome and keys for differential diagnosis. J Clin Endocrinol Metab 83:1455–1461

    Article  PubMed  CAS  Google Scholar 

  • Sempoux C, Guiot Y, Noel H, Jaubert F, Rahier J (2002) Persistent hyperinsulinemic hypoglycemia of infancy: the pathologist’s experience. Ann Pathol 22:375–386

    PubMed  Google Scholar 

  • Sempoux C, Guiot Y, Dahan K, Moulin P, Stevens M, Lambot V, Lonlay P de, Fournet JC, Junien C, Jaubert F, Nihoul-Fékété C, Saudubray JM, Rahier J (2003) The focal form of persistent hyperinsulinaemic hypoglycaemia of infancy: morphological and molecular studies show structural and functional differences with insulinoma. Diabetes 52:784–794

    Article  PubMed  CAS  Google Scholar 

  • Shih DQ, Heimesaat M, Kuwajima S, Stein R, Wright CV, Stoffel M (2002) Profound defects in pancreatic β-cell function in mice with combined heterozygous mutations in Pdx-1, Hnf-1α and Hnf-3 β. Proc Natl Acad Sci USA 99:3818–3823

    Article  PubMed  CAS  Google Scholar 

  • Shyng S, Nichols CG (1997) Octameric stoichiometry of the KATP channel complex. J Gen Physiol 110:655–664

    Article  PubMed  CAS  Google Scholar 

  • Stanley CA, Lieu YK, Hsu BY, Burlina AB, Greenberg CR, Hopwood NJ, Perlman K, Rich BH, Zammarchi E, Poncz M (1998) Hyperinsulinism and hyperammonemia in infant with regulatory mutations of the glutamate dehydrogenase gene. N Engl J Med 338:1352–1357

    Article  PubMed  CAS  Google Scholar 

  • Szollosi A, Nenquin M, Henquin JC (2007) Overnight culture unmasks glucose-induced insulin secretion in mouse islets lacking ATP-sensitive K+ channels by improving the triggering Ca2+ signal. J Biol Chem 282:14768–14776

    Article  PubMed  CAS  Google Scholar 

  • Thomas P, Ye Y, Lightner E (1996) Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet 5:1809–1812

    Article  PubMed  CAS  Google Scholar 

  • Tornovsky S, Crane A, Cosgrove KE, Hussain K, Lavie J, Heyman M, Nesher Y, Kuchinski N, Ben-Shushan E, Shatz O, Nahari E, Potikha T, Zangen D, Tenenbaum-Rakover Y, Vries L de, Argente J, Gracia R, Landau H, Eliakim A, Lindley K, Dunne MJ, Aguilar-Bryan L, Glaser B (2004) Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity. J Clin Endocrinol Metab 89:6224–6234

    Article  PubMed  CAS  Google Scholar 

  • Winarto A, Miki T, Seino S, Iwanaga T (2001) Morphological changes in pancreatic islets of KATP channel-deficient mice: the involvement of KATP channels in the survival of insulin cells and the maintenance of islet architecture. Arch Histol Cytol 64:59–67

    Article  PubMed  CAS  Google Scholar 

  • Yamagata K, Nammo T, Moriwaki M, Ihara A, Lizuka K, Yang Q, Satoh T, Li M, Uenaka R, Okita K, Iwahashi H, Zhu Q, Cao Y, Imagawa A, Tochino Y, Hanafusa T, Miyagawa JI, Matsuzawa Y (2002) Overexpression of dominant-negative mutant hepatocyte nuclear factor-1α in pancreatic β-cells causes abnormal islet architecture with decreased expression of e-cadherin, reduced β-cell proliferation, and diabetes. Diabetes 51:114–123

    Article  PubMed  CAS  Google Scholar 

  • Zhang C, Moriguchi T, Kajihara M, Esaki R, Harada A, Shimohata H, Oishi H, Hamada M, Morito N, Hasegawa K, Kudo T, Engel JD, Yamamoto M, Takahashi S (2005) MafA is a key regulator of glucose-stimulated insulin secretion. Mol Cell Biol 25:4969–4976

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We thank M. Stevens and M. Nenquin for expert technical assistance and Dr. C. de Burbure for revising the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yves Guiot.

Additional information

This work was supported by grants 3.4616.05 (J.R.) and 9.4559.04 (C.S.) from the Fonds National de la Recherche Scientifique, Brussels, and by grant ARC 05/10–328 (I.M. and C.S.) from the Direction de la Recherche Scientifique de la Communauté Française de Belgique.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Marhfour, I., Moulin, P., Marchandise, J. et al. Impact of Sur1 gene inactivation on the morphology of mouse pancreatic endocrine tissue. Cell Tissue Res 335, 505–515 (2009). https://doi.org/10.1007/s00441-008-0733-2

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00441-008-0733-2

Keywords

Navigation