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首页> 外文期刊>BMC Developmental Biology >Reduced-folate carrier (RFC) is expressed in placenta and yolk sac, as well as in cells of the developing forebrain, hindbrain, neural tube, craniofacial region, eye, limb buds and heart
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Reduced-folate carrier (RFC) is expressed in placenta and yolk sac, as well as in cells of the developing forebrain, hindbrain, neural tube, craniofacial region, eye, limb buds and heart

机译:减少叶酸的载体(RFC)在胎盘和卵黄囊以及发育中的前脑,后脑,神经管,颅面区域,眼睛,四肢芽和心脏的细胞中表达

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Background Folate is essential for cellular proliferation and tissue regeneration. As mammalian cells cannot synthesize folates de novo, tightly regulated cellular uptake processes have evolved to sustain sufficient levels of intracellular tetrahydrofolate cofactors to support biosynthesis of purines, pyrimidines, and some amino acids (serine, methionine). Though reduced-folate carrier (RFC) is one of the major proteins mediating folate transport, knowledge of the developmental expression of RFC is lacking. We utilized in situ hybridization and immunolocalization to determine the developmental distribution of RFC message and protein, respectively. Results In the mouse, RFC transcripts and protein are expressed in the E10.0 placenta and yolk sac. In the E9.0 to E11.5 mouse embryo RFC is widely detectable, with intense signal localized to cell populations in the neural tube, craniofacial region, limb buds and heart. During early development, RFC is expressed throughout the eye, but by E12.5, RFC protein becomes localized to the retinal pigment epithelium (RPE). Conclusions Clinical studies show a statistical decrease in the number of neural tube defects, craniofacial abnormalities, cardiovascular defects and limb abnormalities detected in offspring of female patients given supplementary folate during pregnancy. The mechanism, however, by which folate supplementation ameliorates the occurrence of developmental defects is unclear. The present work demonstrates that RFC is present in placenta and yolk sac and provides the first evidence that it is expressed in the neural tube, craniofacial region, limb buds and heart during organogenesis. These findings suggest that rapidly dividing cells in the developing neural tube, craniofacial region, limb buds and heart may be particularly susceptible to folate deficiency.
机译:背景叶酸对于细胞增殖和组织再生至关重要。由于哺乳动物细胞无法从头合成叶酸,因此严格控制的细胞摄取过程已发展为维持足够水平的细胞内四氢叶酸辅因子以支持嘌呤,嘧啶和某些氨基酸(丝氨酸,蛋氨酸)的生物合成。尽管还原叶酸载体(RFC)是介导叶酸转运的主要蛋白质之一,但缺乏有关RFC发育表达的知识。我们利用原位杂交和免疫定位分别确定RFC消息和蛋白质的发育分布。结果在小鼠中,RFC转录本和蛋白质在E10.0胎盘和卵黄囊中表达。在E9.0至E11.5中,可广泛检测到RFC的小鼠胚胎,其强烈信号位于神经管,颅面区域,肢芽和心脏的细胞群体中。在早期发育期间,RFC在整个眼睛中表达,但是通过E12.5,RFC蛋白变得局限于视网膜色素上皮(RPE)。结论临床研究表明,在妊娠期间补充叶酸的女性患者的后代中发现的神经管缺陷,颅面异常,心血管缺陷和肢体异常的数量有统计学意义的减少。然而,叶酸补充改善发育缺陷发生的机理尚不清楚。目前的工作表明,RFC存在于胎盘和卵黄囊中,并提供了第一个证据,表明它在器官发生过程中在神经管,颅面区域,肢芽和心脏中表达。这些发现表明,在发育中的神经管,颅面区域,肢芽和心脏中快速分裂的细胞可能特别易受叶酸缺乏的影响。

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