Gaston-Massuet Carles, Andoniadou Cynthia L, Signore Massimo, Sajedi Ezat, Bird Sophie, Turner James M A, Martinez-Barbera Juan Pedro
Neural Development Unit, Institute of Child Health, University College London, London, UK.
Dev Biol. 2008 Dec 15;324(2):322-33. doi: 10.1016/j.ydbio.2008.08.008. Epub 2008 Aug 18.
Hesx1 has been shown to be essential for normal pituitary development. The homeobox gene Six3 is expressed in the developing pituitary gland during mouse development but its function in this tissue has been precluded by the fact that in the Six3-deficient embryos the pituitary gland is not induced. To gain insights into the function of Six3 during pituitary development we have generated Six3+/- ;Hesx1Cre/+ double heterozygous mice. Strikingly, these mice show marked dwarfism, which is first detectable around weaning, and die by the 5th-6th week of age. Thyroid and gonad development is also impaired in these animals. Analysis of Six3+/- ;Hesx1Cre/+ compound embryos indicates that hypopituitarism is the likely cause of these defects since pituitary development is severely impaired in these mutants. Similar to the Hesx1-deficient embryos, Rathke's pouch is initially expanded in Six3+/- ;Hesx1Cre/+ compound embryos due to an increase in cell proliferation. Subsequently, the anterior pituitary gland appears bifurcated, dysmorphic and occasionally ectopically misplaced in the nasopharyngeal cavity, but cell differentiation is unaffected. Our research has revealed a role for Six3 in normal pituitary development, which has likely been conserved during evolution as SIX3 is also expressed in the pituitary gland of the human embryo.
研究表明,Hesx1对于正常垂体发育至关重要。同源盒基因Six3在小鼠发育过程中的垂体腺中表达,但其在该组织中的功能因Six3基因缺陷胚胎中垂体腺未被诱导这一事实而无法确定。为深入了解Six3在垂体发育过程中的功能,我们构建了Six3+/- ;Hesx1Cre/+双杂合小鼠。令人惊讶的是,这些小鼠表现出明显的侏儒症,在断奶左右首次可被检测到,并在5至6周龄时死亡。这些动物的甲状腺和性腺发育也受到损害。对Six3+/- ;Hesx1Cre/+复合胚胎的分析表明,垂体功能减退可能是这些缺陷的原因,因为这些突变体的垂体发育严重受损。与Hesx1基因缺陷胚胎相似,在Six3+/- ;Hesx1Cre/+复合胚胎中,Rathke囊最初因细胞增殖增加而扩张。随后,垂体前叶出现分叉、形态异常,偶尔在鼻咽腔中异位,但细胞分化未受影响。我们的研究揭示了Six3在正常垂体发育中的作用,由于SIX3也在人类胚胎的垂体腺中表达,这一作用可能在进化过程中得以保留。