首页> 外文期刊>Molecular and Cellular Endocrinology >Expression of the two isoforms of prostaglandin endoperoxide synthase (PGHS-1 and PGHS-2) during adipose cell differentiation.
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Expression of the two isoforms of prostaglandin endoperoxide synthase (PGHS-1 and PGHS-2) during adipose cell differentiation.

机译:脂肪细胞分化过程中前列腺素内过氧化物合酶(PGHS-1和PGHS-2)的两种同工型的表达。

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摘要

Expression of mRNAs encoding the two prostaglandin endoperoxide synthase (PGHS) isoenzymes (PGHS-1 and -2) was investigated in differentiating clonal Ob1771 mouse preadipocytes and in mouse adipose tissues. Northern analysis revealed that the expression level of PGHS-1 mRNA was reduced by 98+/-0.2% (P <0.01) during differentiation of Ob1771 cells, whereas PGHS-2 mRNA was not detected. By reverse transcriptase-polymerase chain reaction analysis, however, both PGHS-1 and -2 mRNA was detected in Ob1771 preadipose cells. In addition. mRNAs encoding both isoforms were markedly expressed in primary adipose precursor cells with considerably lower expression levels in mature adipocytes (56 75% reduction, P<0.01). Furthermore, exposure to dexamethasone (10 nM) for both 24 h (explants of adipose tissue) and 48 h (Ob1771 adipose cells) resulted in enhanced expression of PGHS-1 mRNA. whereas expression of PGHS-2 mRNA in explants of adipose tissue (24 h incubation) was reduced by 83 +/- 9% (P<0.05). In contrast, exposure to angiotensin II (100 nM) enhanced expression of PGHS-1 mRNA both in mature adipocytes (4 h incubation) and explants of adipose tissue (24 h incubation), and elevated PGHS-2 mRNA expression in mature adipocytes (4 h incubation). In conclusion, this report suggests a differential expression of PGHS mRNAs during adipose cell differentiation, and further suggests that the machinery for prostaglandin synthesis in mature adipocytes may be induced by various hormones.
机译:在分化的克隆Ob1771小鼠前脂肪细胞和小鼠脂肪组织中研究了编码这两种前列腺素内过氧化物合酶(PGHS)同工酶(PGHS-1和-2)的mRNA的表达。 Northern分析表明,在Ob1771细胞分化过程中,PGHS-1 mRNA的表达水平降低了98 +/- 0.2%(P <0.01),而未检测到PGHS-2 mRNA。但是,通过逆转录酶-聚合酶链反应分析,在Ob1771脂肪细胞中同时检测到PGHS-1和-2 mRNA。此外。编码这两种同工型的mRNA在原发性脂肪前体细胞中显着表达,而在成熟脂肪细胞中的表达水平则显着降低(降低56 75%,P <0.01)。此外,暴露于地塞米松(10 nM)24小时(脂肪组织外植体)和48小时(Ob1771脂肪细胞)均导致PGHS-1 mRNA表达增强。而PGHS-2 mRNA在脂肪组织(培养24小时)中的表达降低了83 +/- 9%(P <0.05)。相反,暴露于血管紧张素II(100 nM)会增强成熟脂肪细胞(培养4小时)和脂肪组织外植体(培养24小时)中PGHS-1 mRNA的表达,并增加成熟脂肪细胞中PGHS-2 mRNA的表达(4 h孵育)。总之,该报告表明在脂肪细胞分化过程中PGHS mRNA的差异表达,并进一步表明,成熟脂肪细胞中前列腺素合成的机制可能是由多种激素诱导的。

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