No abstract

Vitamin A is essential for normal embryonic cardiogenesis. The vitamin A-deficient phenotype in the avian embryo includes an abnormal heart tube closed at the sinus venosus and the absence of large vessels that normally connect the embryonic heart to the developing circulatory system. In vitamin A-deficient embryos the expression of cardiomyocyte differentiation genes, including atrial-specific myosin heavy chain, ventricular-specific myosin, and sarcomeric myosins as well as the putative cardiomyocyte specification gene Nkx-2.5, is not altered. However, the expression of transcription factor GATA-4 is severely decreased in the heart-forming regions of vitamin A-deficient stage 7-10 embryos. Significantly, GATA-4 transcripts are completely lacking in the lateral mesoderm posterior to the heart, in the area of the developing cardiac inflow tract that later displays prominent morphological defects, including a closed nonseptated heart lacking a sinus venosus. The administration of retinol to the vitamin A-deficient embryo restores GATA-4 expression and completely rescues the vitamin A-deficient phenotype. Our results indicate that GATA-4 is a component of the retinoid-mediated cardiogenic pathway unlinked to cardiomyocyte differentiation, but involved in the morphogenesis of the posterior heart tube and the development of the cardiac inflow tract.

Vitamin A-deficient (VAD) quail embryos have severe abnormalities, including a high incidence of reversed cardiac situs. Using this model we examined in vivo the physiological function of vitamin A in the left/right (L/R) cardiac asymmetry pathway. Molecular analysis reveals the expression of early asymmetry genes activin receptor IIa, sonic hedgehog, Caronte, Lefty-1, and Fgf8 to be unaffected by the lack of retinoids, while expression of the downstream genes nodal-related, snail-related (cSnR), and Pitx2 is altered. In VAD embryos nodal expression in left lateral plate mesoderm (LPM) is severely downregulated and the expression domain altered during neurulation. Similarly, the expression of cSnR in the right LPM and of Pitx2 in the left side posterior heart-forming region (HFR) is downregulated in the VAD embryos. The lack of retinoids does not cause randomization or ectopic expression of nodal, cSnR, or Pitx2. At the six- to eight-somite stage nodal is expressed transiently in the left posterior HFR of normal quail embryos; this expression is missing in VAD embryos and may be linked to the loss of Pitx2 expression in this region of VAD quail embryos. Administration of retinoids to VAD embryos prior to the six-somite stage rescues the expression of nodal, cSnR, and Pitx2 as well as the randomized VAD cardiac phenotype. There is an absolute requirement for retinoids at the four- to five-somite developmental window for cardiogenesis and cardiac L/R specification to proceed normally. We conclude that retinoids do not regulate the left/right-specific sidedness assignments for expression of genes on the vertebrate cardiac asymmetry pathway, but are required during neurulation for the maintenance of adequate levels of their expression and for the development of the posterior heart tube and a loopable heart. Cardiac asymmetry may be but one of several critical events regulated by retinoid signaling in the retinoid-sensitive developmental window.

Vitamin A requirement for early embryonic development is clearly evident in the gross cardiovascular and central nervous system abnormalities and an early death of the vitamin A-deficient quail embryo. This retinoid knockout model system was used to examine the biological activity of various natural retinoids in early cardiovascular development. We demonstrate that all-trans-, 9-cis-, 4-oxo-, and didehydroretinoic acids, and didehydroretinol and all-trans-retinol induce and maintain normal cardiovascular development as well as induce expression of the retinoic acid receptor beta2 in the vitamin A-deficient quail embryo. The expression of RARbeta2 is at the same level and at the same sites where it is expressed in the normal embryo. Retinoids provided to the vitamin A-deficient embryo up to the 5-somite stage of development, but not later, completely rescue embryonic development, suggesting the 5-somite stage as a critical retinoid-sensitive time point during early avian embryogenesis. Retinoid receptors RARalpha, RARgamma, and RXRalpha are expressed in both the precardiac endoderm and mesoderm in the normal and the vitamin A-deficient quail embryo, while the expression of RXRgamma is restricted to precardiac endoderm. Vitamin A deficiency downregulates the expression of RARalpha and RARbeta. Our studies provide strong evidence for a narrow retinoid-requiring developmental window during early embryogenesis, in which the presence of bioactive retinoids and their receptors is essential for a subsequent normal embryonic development.

Vitamin A requirement for early embryonic development is clearly evident in the gross cardiovascular and central nervous system abnormalities and an early death of the vitamin A‐deficient quail embryo. This retinoid knockout model system was used to examine the biological activity of various natural retinoids in early cardiovascular development. We demonstrate that all‐trans‐, 9‐cis‐, 4‐oxo‐, and didehydroretinoic acids, and didehydroretinol and all‐trans‐retinol induce and maintain normal cardiovascular development as well as induce expression of the retinoic acid receptor β2 in the vitamin A‐deficient quail embryo. The expression of RARβ2 is at the same level and at the same sites where it is expressed in the normal embryo. Retinoids provided to the vitamin A‐deficient embryo up to the 5‐somite stage of development, but not later, completely rescue embryonic development, suggesting the 5‐somite stage as a critical retinoid‐sensitive time point during early avian embryogenesis. Retinoid receptors RARα, RARγ, and RXRα are expressed in both the precardiac endoderm and mesoderm in the normal and the vitamin A‐deficient quail embryo, while the expression of RXRγ is restricted to precardiac endoderm. Vitamin A deficiency downregulates the expression of RARα and RARβ. Our studies provide strong evidence for a narrow retinoid‐requiring developmental window during early embryogenesis, in which the presence of bioactive retinoids and their receptors is essential for a subsequent normal embryonic development. Dev. Dyn. 1998;213:188–198. © 1998 Wiley‐Liss, Inc.

Модель ретиноїдного нокауту використано для перевірки біологічної активності деяких природних ретиноїдів під час ембріонального розвитку серцево-судинної системи. Показано, що all-trans-, 9-cis-, 4-оксо-та дидегідро-ретиноєва кислоти, а також all-trans-ретинол здатні самостійно підтримувати її нормальний розвиток. Дефіцитні за вітаміном А ембріони розвивалися нормаль но лише за умови, якщо ретоноїди додавали на ранніх етапах ембріогенезу, не пізніше формування п'ятого соміту. Дефіцит вітаміну А протягом ембріонального розвитку суттєво знижує рівень експресії рецептора ретиноєвої кислоти ЯАНвг як у серці, так і в центральній нервовій системі. ,Всі використані нами ретиоїди індукують експресію ЯАНвг у вітамін А-дефіцитних ембріонів куріпок в тих же ембріональних структурах, що і в нормальних ембріонів, але на різному рівні. Таким чином, наші дані вказують на цілковиту залежність раннього ембріогенезу птахів від наявності відповідних ретиноїдів, а також їхніх рецепторів. Ключові слова серцево-судинна система, ретиноїди, дефіцит вітаміну А, рецептор ретиноєвої кислоти, ранній ембріогенез.