Insulin receptor knockout mice

被引:178
作者
Kitamura, T [1 ]
Kahn, CR
Accili, E
机构
[1] Columbia Univ, Coll Phys & Surg, Naomi Berrie Diabet Ctr, Dept Med, New York, NY 10032 USA
[2] Harvard Univ, Sch Med, Joslin Diabet Ctr, Boston, MA 02215 USA
关键词
diabetes; genetics; signal transduction; beta-cell; animal models;
D O I
10.1146/annurev.physiol.65.092101.142540
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
To examine the role of the insulin receptor in fuel homeostasis, we and others have carried out genetic ablation studies in mice. Mice lacking insulin receptors are born. with normal features, but develop early postnatal diabetes and die of ketoacidosis. In contrast, mice lacking insulin receptors in specific cell types as a result of conditional mutagenesis develop mild metabolic and reproductive abnormalities. These experiments have uncovered novel functions of insulin receptors in tissues such as brain and pancreatic beta-cells. Combined knockout studies of insulin and Igf1 receptors indicate that the insulin receptor also promotes embryonic growth. Experimental crosses of mice with insulin receptor haploinsufficiency have been instrumental to the genetic analysis of insulin action by enabling us to assign specific roles to different insulin receptor substrates and identify novel elements in insulin signaling.
引用
收藏
页码:313 / 332
页数:22
相关论文
共 129 条
  • [31] Fisher SJ, 2001, DIABETES, V50, pA50
  • [32] Insulin receptor isoform A, a newly recognized, high-affinity insulin-like growth factor II receptor in fetal and cancer cells
    Frasca, F
    Pandini, C
    Scalia, P
    Sciacca, L
    Mineo, R
    Costantino, A
    Goldfine, ID
    Belfiore, A
    Vigneri, R
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1999, 19 (05) : 3278 - 3288
  • [33] REVERSIBILITY OF DEFECTIVE ADIPOCYTE INSULIN-RECEPTOR KINASE-ACTIVITY IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS - EFFECT OF WEIGHT-LOSS
    FREIDENBERG, GR
    REICHART, D
    OLEFSKY, JM
    HENRY, RR
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (04) : 1398 - 1406
  • [34] Hypoglycaemia, liver necrosis and perinatal death in mice lacking all isoforms of phosphoinositide 3-kinase p85α
    Fruman, DA
    Mauvais-Jarvis, F
    Pollard, DA
    Yballe, CM
    Brazil, D
    Bronson, RT
    Kahn, CR
    Cantley, LC
    [J]. NATURE GENETICS, 2000, 26 (03) : 379 - 382
  • [35] Ghosh S, 1996, ANNU REV MED, V47, P333
  • [36] ADAPTATIONS OF GLUCOSE AND FATTY-ACID METABOLISM DURING PERINATAL-PERIOD AND SUCKLING-WEANING TRANSITION
    GIRARD, J
    FERRE, P
    PEGORIER, JP
    DUEE, PH
    [J]. PHYSIOLOGICAL REVIEWS, 1992, 72 (02) : 507 - 562
  • [37] FACTORS AFFECTING SECRETION OF INSULIN AND GLUCAGON BY RAT FETUS
    GIRARD, JR
    KERVRAN, A
    SOUFFLET, E
    ASSAN, R
    [J]. DIABETES, 1974, 23 (04) : 310 - 317
  • [38] OXIDATIVE AND NON-OXIDATIVE GLUCOSE-METABOLISM IN NON-OBESE TYPE-2 (NON-INSULIN-DEPENDENT) DIABETIC-PATIENTS
    GOLAY, A
    DEFRONZO, RA
    FERRANNINI, E
    SIMONSON, DC
    THORIN, D
    ACHESON, K
    THIEBAUD, D
    CURCHOD, B
    JEQUIER, E
    FELBER, JP
    [J]. DIABETOLOGIA, 1988, 31 (08) : 585 - 591
  • [39] GOTTLIEB S, 1994, GENETICS, V137, P107
  • [40] TRANSGENIC KNOCKOUTS REVEAL A CRITICAL REQUIREMENT FOR PANCREATIC BETA-CELL GLUCOKINASE IN MAINTAINING GLUCOSE-HOMEOSTASIS
    GRUPE, A
    HULTGREN, B
    RYAN, A
    MA, YH
    BAUER, M
    STEWART, TA
    [J]. CELL, 1995, 83 (01) : 69 - 78