Thioredoxin binding protein-2 inhibits excessive fetal hypoglycemia during maternal starvation by suppressing insulin secretion in mice

Pediatr Res. 2010 Feb;67(2):138-43. doi: 10.1203/PDR.0b013e3181c2f4cc.

Abstract

Glucose is a major fuel for fetal development. Fetal blood glucose level is mainly dependent on maternal blood glucose concentration, though it is also regulated by fetal insulin level. Thioredoxin binding protein-2 (TBP-2), which is identical to vitamin D3 up-regulated protein (VDUP1) and thioredoxin interacting protein (Txnip), was recently reported to be a key transcriptional factor controlling glucose metabolism. Here, we elucidated the functions of TBP-2 in maintaining blood glucose homeostasis during the fetal period. TBP-2(+/-) female mice were mated with TBP-2(+/-) male mice; beginning 16.5-d post coitum, pregnant mice were fed or fasted for 24 h. Under conditions of maternal starvation, the blood glucose levels of TBP-2(-/-) fetuses were significantly lower than those of TBP-2(+/+) fetuses, corresponding to the elevated plasma insulin levels of TBP-2(-/-) fetuses compared with those of TBP-2(+/+) fetuses. There was no difference between TBP-2(+/+) and TBP-2(-/-) fetuses in terms of their pancreatic beta-cell masses or the expression of placental glucose transporters under conditions of either maternal feeding or fasting. Thus, during maternal fasting, fetal TBP-2 suppresses excessive insulin secretion to maintain the fetus's glucose levels, implying that TBP-2 is a critical molecule in mediating fetal glucose homeostasis depending on nutrient availability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animal Nutritional Physiological Phenomena*
  • Animals
  • Blood Glucose / metabolism*
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Disease Models, Animal
  • Down-Regulation
  • Female
  • Fetal Blood / metabolism
  • Fetal Nutrition Disorders / blood
  • Fetal Nutrition Disorders / genetics
  • Fetal Nutrition Disorders / prevention & control*
  • Fetal Weight
  • Gene Expression Regulation
  • Gestational Age
  • Gluconeogenesis / genetics
  • Homeostasis
  • Hypoglycemia / blood
  • Hypoglycemia / embryology
  • Hypoglycemia / genetics
  • Hypoglycemia / prevention & control*
  • Insulin / blood*
  • Insulin-Secreting Cells / metabolism
  • Lactic Acid / blood
  • Liver / embryology
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Pancreas / embryology
  • Pancreas / metabolism
  • Placenta / pathology
  • Pregnancy
  • Prenatal Nutritional Physiological Phenomena*
  • Starvation / blood
  • Starvation / complications*
  • Starvation / genetics
  • Thioredoxins / genetics
  • Thioredoxins / metabolism*

Substances

  • Blood Glucose
  • Carrier Proteins
  • Insulin
  • Txnip protein, mouse
  • Lactic Acid
  • Thioredoxins