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肺铁蛋白:高氧肺损伤对亚基mRNA水平的不同影响。

Pulmonary ferritin: differential effects of hyperoxic lung injury on subunit mRNA levels.

作者信息

Ryan T P, Krzesicki R F, Blakeman D P, Chin J E, Griffin R L, Richards I M, Aust S D, Petry T W

机构信息

Upjohn Laboratories, Kalamazoo, MI 49001, USA.

出版信息

Free Radic Biol Med. 1997;22(5):901-8. doi: 10.1016/s0891-5849(96)00483-2.

Abstract

Ferritin is an iron storage protein that is regulated at the transcriptional and transcriptional levels, resulting in a complex mixture of tissue- and condition-specific isoforms. The protein shell of ferritin is composed of 24 subunits of two types (heavy or light), which are encoded by two distinct and independently regulated genes. In the present studies, the isoform profile for lung ferritin differed from other tissues (liver, spleen, and heart) as determined by isoelectric focusing (IEF) and polyacrylamide gel electrophoresis (PAGE). Lung ferritin was composed of equal amounts of heavy and light subunits. Differences in isoform profiles were the result of tissue-specific differential expression of the ferritin subunit genes as demonstrated by Northern blot analyses. Like heart ferritin, lung ferritin exhibited a low iron content that did not increase extensively in response to iron challenge, which contrasts with ferritins isolated from liver or spleen. When animals were exposed to hyperoxic conditions (95% oxygen for up to 60 h), ferritin heavy subunit mRNA levels did not markedly change at any of the investigated time points. In contrast, ferritin light subunit mRNA increased severalfold in response to hyperoxic exposure. Investigation of the cytoplasmic distribution of ferritin mRNA showed that a substantial portion was associated with the ribonucleoprotein (RNP) fraction of the cytosol, suggesting that a pool of untranslated ferritin mRNA exists in the lung. Upon hyperoxic insult, all ferritin light subunit mRNA pools (RNP, monosomal, polysomal) were elevated, although a specific shift from RNP to polysomal pools was not evident. Therefore, the increase in translatable ferritin mRNA in response to hyperoxia resulted from transcriptional rather than specific translational activation. The observed pattern of light chain-specific transcriptional induction of ferritin is consistent with the hypothesis that hyperoxic lung injury is at least partially iron mediated.

摘要

铁蛋白是一种铁储存蛋白,其在转录和转录后水平受到调控,导致形成组织和条件特异性异构体的复杂混合物。铁蛋白的蛋白质外壳由两种类型(重链或轻链)的24个亚基组成,这两种亚基由两个不同且独立调控的基因编码。在本研究中,通过等电聚焦(IEF)和聚丙烯酰胺凝胶电泳(PAGE)测定,肺铁蛋白的异构体谱与其他组织(肝脏、脾脏和心脏)不同。肺铁蛋白由等量的重链和轻链亚基组成。如Northern印迹分析所示,异构体谱的差异是铁蛋白亚基基因组织特异性差异表达的结果。与心脏铁蛋白一样,肺铁蛋白的铁含量较低,对铁刺激没有明显增加,这与从肝脏或脾脏分离的铁蛋白形成对比。当动物暴露于高氧条件(95%氧气,长达60小时)时,在任何研究时间点铁蛋白重链亚基mRNA水平均无明显变化。相反,铁蛋白轻链亚基mRNA在高氧暴露后增加了几倍。对铁蛋白mRNA胞质分布的研究表明,相当一部分与细胞质的核糖核蛋白(RNP)部分相关,这表明肺中存在未翻译的铁蛋白mRNA池。在高氧损伤后,所有铁蛋白轻链亚基mRNA池(RNP、单体、多聚体)均升高,尽管从RNP池到多聚体池的特异性转变并不明显。因此,高氧反应中可翻译铁蛋白mRNA的增加是由转录而非特异性翻译激活引起的。观察到的铁蛋白轻链特异性转录诱导模式与高氧肺损伤至少部分由铁介导的假说一致。

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