Gatford Kathryn L, Mohammad Saidatul N B, Harland M Lyn, De Blasio Miles J, Fowden Abigail L, Robinson Jeffrey S, Owens Julie A
Research Centre for Early Origins of Adult Disease, Discipline of Obstetrics and Gynaecology, School of Paediatrics and Reproductive Health, University of Adelaide, South Australia 5005, Australia.
Endocrinology. 2008 Oct;149(10):5118-27. doi: 10.1210/en.2008-0233. Epub 2008 Jun 5.
Poor growth before birth increases the risk of non-insulin-dependent diabetes mellitus (NIDDM) and impairs insulin secretion relative to sensitivity. We investigated the effects of intrauterine growth restriction in sheep on insulin secretion, beta-cell mass, and function from before birth to young adulthood and its molecular basis. Pancreas was collected from control and placentally restricted sheep as fetuses (d 143 gestation), lambs (aged 42 d), and young adults (aged 556 d), following independent measures of in vivo insulin secretion and sensitivity. beta-Cells and islets were counted after immunohistochemical staining for insulin. In lambs, gene expression was measured by RT-PCR and expressed relative to 18S. beta-Cell mass correlated positively with fetal weight but negatively with birth weight in adult males. Glucose-stimulated insulin disposition and beta-cell function correlated negatively with fetal weight but positively with birth weight in adult males. Placental restriction increased pancreatic expression of IGF-II and IGF-I but decreased that of voltage-gated calcium channel, alpha1D subunit (CACNA1D) in lambs. In male lambs, pancreatic IGF-II and insulin receptor expression correlated strongly and positively with beta-cell mass and CACNA1D expression with glucose-stimulated insulin disposition. Restricted growth before birth in the sheep does not impair insulin secretion, relative to sensitivity, before birth or in young offspring. IGF-II and insulin receptor are implicated as key molecular regulators of beta-cell mass compensation, whereas impaired expression of the voltage-gated calcium channel may underlie impaired beta-cell function after intrauterine growth restriction. With aging, the insulin secretory capacity of the beta-cell is impaired in males, and their increases in beta-cell mass are inadequate to maintain adequate insulin secretion relative to sensitivity.
出生前生长发育不良会增加非胰岛素依赖型糖尿病(NIDDM)的风险,并相对于敏感性损害胰岛素分泌。我们研究了绵羊子宫内生长受限对从出生前到青年期胰岛素分泌、β细胞质量和功能的影响及其分子基础。在对体内胰岛素分泌和敏感性进行独立测量后,从对照羊和胎盘受限羊中收集胰腺,分别作为胎儿(妊娠143天)、羔羊(42日龄)和青年羊(556日龄)。对胰岛素进行免疫组织化学染色后,对β细胞和胰岛进行计数。在羔羊中,通过RT-PCR测量基因表达,并相对于18S进行表达。成年雄性中,β细胞质量与胎儿体重呈正相关,但与出生体重呈负相关。葡萄糖刺激的胰岛素处置和β细胞功能与胎儿体重呈负相关,但与成年雄性的出生体重呈正相关。胎盘受限增加了羔羊胰腺中IGF-II和IGF-I的表达,但降低了电压门控钙通道α1D亚基(CACNA1D)的表达。在雄性羔羊中,胰腺IGF-II和胰岛素受体表达与β细胞质量呈强正相关,而CACNA1D表达与葡萄糖刺激的胰岛素处置呈正相关。绵羊出生前生长受限相对于敏感性而言,在出生前或幼年后代中不会损害胰岛素分泌。IGF-II和胰岛素受体被认为是β细胞质量补偿的关键分子调节因子,而电压门控钙通道表达受损可能是子宫内生长受限后β细胞功能受损的基础。随着年龄增长,雄性β细胞的胰岛素分泌能力受损,其β细胞质量的增加不足以维持相对于敏感性而言足够的胰岛素分泌。