Zile M H
Department of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, USA.
J Nutr. 2001 Mar;131(3):705-8. doi: 10.1093/jn/131.3.705.
Advances in molecular biology and retinoic acid receptor research have significantly contributed to the understanding of the role of vitamin A during vertebrate development. Examination of the function of this vitamin during very early developmental stages using the completely vitamin A-depleted avian embryo has revealed that the vitamin A requirement begins at the time of formation of the primitive heart, circulation and specification of hindbrain. The lack of vitamin A at this critical time results in gross abnormalities and early embryonic death. In rodent models, vitamin A deficiency can be targeted to later gestational windows and documents the need for vitamin A for more advanced stages of development. Major target tissues of vitamin A deficiency include the heart, central nervous system and structures derived from it, the circulatory, urogenital and respiratory systems, and the development of skull, skeleton and limbs. These abnormalities are also evident in mice mutants from retinoid receptor knockouts; they have revealed both morphological and molecular aspects of vitamin A function during development. Retinoic acid receptors (RAR) in partnership with retinoid X receptor (RXR)alpha appear to be the important retinoid receptor transcription factors regulating vitamin A function at the gene level during development via the physiologic ligand all-trans-retinoic acid. Homeostasis of retinoic acid is maintained by developmentally regulated vitamin A metabolism enzyme systems. Inadequate vitamin A nutrition during early pregnancy may account for some pediatric congenital abnormalities.
分子生物学和视黄酸受体研究的进展对理解维生素A在脊椎动物发育过程中的作用做出了重大贡献。利用完全缺乏维生素A的鸡胚对该维生素在非常早期发育阶段的功能进行研究发现,维生素A的需求始于原始心脏形成、循环系统出现以及后脑特化之时。在这个关键时期缺乏维生素A会导致严重畸形和胚胎早期死亡。在啮齿动物模型中,维生素A缺乏可针对妊娠后期阶段,这证明了发育更高级阶段对维生素A的需求。维生素A缺乏的主要靶组织包括心脏、中枢神经系统及其衍生结构、循环系统、泌尿生殖系统和呼吸系统,以及颅骨、骨骼和四肢的发育。这些异常在视黄酸受体基因敲除的小鼠突变体中也很明显;它们揭示了发育过程中维生素A功能的形态学和分子学方面。视黄酸受体(RAR)与视黄酸X受体(RXR)α协同作用,似乎是在发育过程中通过生理配体全反式视黄酸在基因水平调节维生素A功能的重要视黄酸受体转录因子。视黄酸的稳态由发育调控的维生素A代谢酶系统维持。妊娠早期维生素A营养不足可能是一些儿童先天性异常的原因。