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首页> 外文期刊>International Journal of Clinical and Experimental Medicine >Milk fat globule-EGF factor 8 mRNA expression in rat splanchnic tissues during postnatal development
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Milk fat globule-EGF factor 8 mRNA expression in rat splanchnic tissues during postnatal development

机译:产后发育过程中大鼠内脏组织中乳脂球EGF因子8 mRNA的表达

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Milk fat globule-EGF factor (MFG-E8) is a protein that binds to αvβ3/5 integrin and phosphatidylserine. It plays a role in apoptotic cell removal, tissue remodeling and intestinal epithelial wound-healing process. In the present study, we examined the expression of MFG-E8 mRNA in the small intestine, liver and lungs during postnatal development. Sprague-Dawley rats were sacrificed at different ages (E20, P0, P5, P10 and P21). Total RNA was extracted from various tissues including the small intestine, liver and lungs. The MFG-E8 mRNA expression was quantified by real-time PCR. We found that the MFG-E8 mRNA was expressed at a low level on E20 in the liver. Within 24 hours after birth, its expression was markedly increased. It was then stably expressed at high level during the postnatal period. In contrast, in the small intestine, MFG-E8 mRNA significantly decreased by more than 60% (p<0.001) within 24 hours after birth compared to E20, then it gradually regained E20 values by P10. It was persistently expressed until P21. In the lungs, MFG-E8 is constitutively expressed prenatally at E20. Its expression did not change during the postnatal period. In summary, our study indicated that MFG-E8 is extensively expressed in the small intestine, liver, and lungs. As opposed to other organs, the expression of intestinal MFG-E8 is decreased during the first week of life. It is possible that this could contribute to the predisposition of the neonatal intestine to inflammation.
机译:乳脂球EGF因子(MFG-E8)是一种与α vβ 3/5整联蛋白和磷脂酰丝氨酸结合的蛋白质。它在凋亡细胞去除,组织重塑和肠上皮伤口愈合过程中发挥作用。在本研究中,我们检查了产后发育过程中MFG-E8 mRNA在小肠,肝和肺中的表达。处死不同年龄(E20,P0,P5,P10和P21)的Sprague-Dawley大鼠。从包括小肠,肝和肺在内的各种组织中提取总RNA。通过实时PCR定量MFG-E8 mRNA表达。我们发现,MFG-E8 mRNA在肝脏中的E20上低水平表达。出生后24小时内,其表达明显增加。然后在产后稳定表达高水平。相反,在小肠中,与E20相比,MFG-E8 mRNA在出生后24小时内显着降低了60%以上(p< 0.001),然后通过P10逐渐恢复E20值。一直表达到P21。在肺中,MFG-E8在产前E20时组成性表达。它的表达在产后期间没有改变。总而言之,我们的研究表明MFG-E8在小肠,肝脏和肺中广泛表达。与其他器官相反,肠道MFG-E8的表达在生命的第一周下降。这可能会导致新生儿肠道易发炎。

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