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首页> 外文期刊>Acta Biochimica Polonica >Expression of cellular retinoic acid-binding protein I and II (CRABP I and II) in embryonic mouse hearts treated with retinoic acid
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Expression of cellular retinoic acid-binding protein I and II (CRABP I and II) in embryonic mouse hearts treated with retinoic acid

机译:维甲酸处理的胚胎小鼠心脏中细胞维甲酸结合蛋白I和II(CRABP I和II)的表达

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摘要

Cellular retinoic acid binding proteins are considered to be involved in retinoic acid (RA) signaling pathways. Our aim was to compare the expression and localization of cellular retinoic acid binding proteins I and II (CRABP I and II) in embryonic mouse hearts during normal development and after a single teratogenic dose of RA. Techniques such as real-time PCR, RT-PCR, Western blots and immunostaining were employed to examine hearts from embryos at 9-17 dpc. RA treatment at 8.5dpc affects production of CRABP I and II in the heart in the 48-h period. Changes in expression of mRNA for retinaldehyde dehydrogenase II (Raldh2), Crabp1 and Crabp2 genes also occur within the same time window (i.e. 10-11dpc) after RA treatment. In the embryonic control heart these proteins are localized in groups of cells within the outflow tract (OT), and the atrioventricular endocardial cushions. A gradient of labeling is observed with CRABP II but not for CRABP I along the myocardium of the looped heart at 11 dpc; this gradient is abolished in hearts treated with RA, whereas an increase of RALDH2 staining has been observed at 10 dpc in RA-treated hearts. Some populations of endocardial endothelial cells were intensively stained with anti-CRABP II whereas CRABP I was negative in these structures. These results suggest that CRABP I and II are independently regulated during heart development, playing different roles in RA signaling, essential for early remodeling of the heart tube and alignment of the great arteries to their respective ventricles.
机译:细胞视黄酸结合蛋白被认为与视黄酸(RA)信号通路有关。我们的目的是比较在正常发育过程中和单剂量致畸剂量的RA后胚胎小鼠心脏中细胞视黄酸结合蛋白I和II(CRABP I和II)的表达和定位。实时PCR,RT-PCR,Western印迹和免疫染色等技术被用来检查9-17 dpc的胚胎心脏。 8.5dpc的RA治疗会在48小时内影响心脏中CRABP I和II的产生。视黄醛脱氢酶II(Raldh2),Crabp1和Crabp2基因的mRNA表达变化也发生在RA治疗后的同一时间范围内(即10-11dpc)。在胚胎控制心脏中,这些蛋白质位于流出道(OT)和房室心内膜垫中的细胞组中。 CRABP II在11 dpc时沿环状心脏的心肌观察到标记梯度,但CRABP I观察不到。在用RA治疗的心脏中,这种梯度消失了,而在用RA治疗的心脏中,在10 dpc处观察到RALDH2染色的增加。一些心内膜内皮细胞群体被抗CRABP II强烈染色,而CRABP I在这些结构中呈阴性。这些结果表明,CRABP I和II在心脏发育过程中受到独立调节,在RA信号传导中发挥不同的作用,这对于心管的早期重塑以及大动脉与其各自心室的对齐至关重要。

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