Association of childhood type 1 diabetes mellitus with a variant of PAX4:: possible link to beta cell regenerative capacity

被引:51
作者
Biason-Lauber, A
Boehm, B
Lang-Muritano, M
Gauthier, BR
Brun, T
Wollheim, CB
Schoenle, EJ
机构
[1] Univ Zurich, Childrens Hosp, Dept Paediat Endocrinol Diabetol, CH-8032 Zurich, Switzerland
[2] Univ Ulm, Ulm, Germany
[3] Univ Geneva, Ctr Med, CH-1211 Geneva, Switzerland
关键词
diabetes mellitus; type; 1; pancreas; regeneration;
D O I
10.1007/s00125-005-1723-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis: Loss of pancreatic beta cells is the crucial event in the development of type 1 diabetes. It is the result of an imbalance between autoimmune destruction and insufficient regeneration of islet cells. To study the role of islet cell regeneration in the pathogenesis of type 1 diabetes, we focused on PAX4, a paired homeodomain transcriptional repressor that is involved in islet cell growth. Methods: The study included 379 diabetic children and 1,070 controls from two distinct populations, and a cohort of children who had not developed type 1 diabetes, despite the presence of islet cell antibodies. Genomic DNA analysis of PAX4 was carried out via direct sequencing of PCR-amplified fragments and allelic discrimination. We compared the transrepression potential of the PAX4 variants in beta TC3 cells and analysed their influence on beta cell growth. Results: The type 1 diabetic subjects are different from the normal individuals in terms of the genotype distribution of the A1168C single nucleotide polymorphism in PAX4. The C/C genotype is frequent among type 1 diabetic children (73%) and rare among the control population (32%). Conversely, the A/C genotype is prevalent among control subjects (62%) and antibody-positive children without type 1 diabetes (73.6%), but uncommon among subjects with type 1 diabetes (17.5%). The combination of PAX4A and PAX4C is functionally more active than PAX4C alone (the 'diabetic' variant). Beta cells expressing PAX4A and PAX4C efficiently proliferate when stimulated with glucose, whereas cells expressing the PAX4C variant alone do not. Conclusions/interpretation: We have identified a link between beta cell regenerative capacity and susceptibility to type 1 diabetes. This finding could explain the fact that not all of the individuals who develop autoimmunity against beta cells actually contract the disease. The C/C genotype of the A1168C polymorphism in PAX4 can be viewed as a predisposition marker that can help to detect individuals prone to develop type 1 diabetes.
引用
收藏
页码:900 / 905
页数:6
相关论文
共 28 条
  • [1] Loss of kinase activity in a patient with Wolcott-Rallison syndrome caused by a novel mutation in the EIF2AK3 gene
    Biason-Lauber, A
    Lang-Muritano, M
    Vaccaro, T
    Schoenle, EJ
    [J]. DIABETES, 2002, 51 (07) : 2301 - 2305
  • [2] Life and death of the pancreatic β cells
    Bonner-Weir, S
    [J]. TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2000, 11 (09) : 375 - 378
  • [3] The diabetes-linked transcription factor PAX4 promotes β-cell proliferation and survival in rat and human islets
    Brun, T
    Franklin, I
    St-Onge, L
    Biason-Louber, A
    Schoenle, EJ
    Wollheim, CB
    Gauthier, BR
    [J]. JOURNAL OF CELL BIOLOGY, 2004, 167 (06) : 1123 - 1135
  • [4] Inhibitory effect of Pax4 on the human insulin and islet amyloid polypeptide (IAPP) promoters
    Campbell, SC
    Cragg, H
    Elrick, LJ
    Macfarlane, WM
    Shennan, KIJ
    Docherty, K
    [J]. FEBS LETTERS, 1999, 463 (1-2): : 53 - 57
  • [5] COOKE A, 1990, CURR TOP MICROBIOL, V164, P125
  • [6] Onset of type I diabetes - A dynamical instability
    De Blasio, BF
    Bak, P
    Pociot, F
    Karlsen, AE
    Nerup, J
    [J]. DIABETES, 1999, 48 (09) : 1677 - 1685
  • [7] A role for activin A and betacellulin in human fetal pancreatic cell differentiation and growth
    Demeterco, C
    Beattie, GM
    Dib, SA
    Lopez, AD
    Hayek, A
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (10) : 3892 - 3897
  • [8] Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation
    Dor, Y
    Brown, J
    Martinez, OI
    Melton, DA
    [J]. NATURE, 2004, 429 (6987) : 41 - 46
  • [9] No evidence of linkage or diabetes-associated mutations in the transcription factors BETA2/NEUROD1 and PAX4 in Type II diabetes in France
    Dupont, S
    Vionnet, N
    Chèvre, JC
    Gallina, S
    Dina, C
    Seino, Y
    Yamada, Y
    Froguel, P
    [J]. DIABETOLOGIA, 1999, 42 (04) : 480 - 484
  • [10] Fujitani Y, 1999, MOL CELL BIOL, V19, P8281