Ashery-Padan Ruth, Zhou Xunlei, Marquardt Till, Herrera Pedro, Toube Leanne, Berry Asher, Gruss Peter
Department of Human Genetics and Molecular Medicine, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 69978 Israel.
Dev Biol. 2004 May 15;269(2):479-88. doi: 10.1016/j.ydbio.2004.01.040.
Pax6 transcription factor is required for islet cell number, morphology, and hormone gene expression. The perinatal lethality of Pax6 null mutants has restricted investigation of the role of Pax6 in normal endocrine cell function. Therefore, we devised the conditional inactivation of Pax6 using the Pdx1 and Pax6 regulatory domains to activate Cre in cells of either the entire pancreatic bud or only in endocrine cell lineages, respectively. Mutant pups died few days after birth, suffering from an overt diabetic phenotype that includes hyperglycemia, hypoinsulinemia, weight loss, and ketosis, indicating an essential role for Pax6 in beta cell function. Glucose-transporter type-2 expression was downregulated, but expression of several transcription factors essential for endocrine development was maintained. Our findings support a role for Pax6 activity in maintaining normal beta cell function after birth, but not for beta cell neogenesis during late embryonic development and early postnatal stages.
胰岛细胞数量、形态及激素基因表达均需要Pax6转录因子。Pax6基因敲除突变体在围产期致死,这限制了对Pax6在正常内分泌细胞功能中作用的研究。因此,我们利用Pdx1和Pax6调控域分别在整个胰腺芽细胞或仅在内分泌细胞谱系中激活Cre,设计了Pax6的条件性失活。突变幼崽出生后几天死亡,表现出明显的糖尿病表型,包括高血糖、低胰岛素血症、体重减轻和酮症,表明Pax6在β细胞功能中起关键作用。2型葡萄糖转运体表达下调,但维持了内分泌发育所需的几种转录因子的表达。我们的研究结果支持Pax6活性在出生后维持正常β细胞功能中发挥作用,但在胚胎发育后期和出生后早期阶段对β细胞新生没有作用。