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叙利亚仓鼠和亚美尼亚仓鼠在血清淀粉样蛋白A基因表达上存在差异。新型叙利亚仓鼠血清淀粉样蛋白A亚型的鉴定。

Syrian and Armenian hamsters differ in serum amyloid A gene expression. Identification of novel Syrian hamster serum amyloid A subtypes.

作者信息

de Beer M C, de Beer F C, Beach C M, Gonnerman W A, Carreras I, Sipe J D

机构信息

Department of Medicine, University of Kentucky College of Medicine, Lexington 40536-0084.

出版信息

J Immunol. 1993 Jun 15;150(12):5361-70.

PMID:8515064
Abstract

Amyloid A (AA) amyloidosis is widespread throughout the animal kingdom. Several factors including: 1) precursor production; 2) precursor structure; 3) precursor degradation; and 4) precursor/product interaction with the pentraxin serum amyloid P have been implicated in amyloidogenesis, but the exact sequence of events leading to AA fibril formation and deposition remains unclear. Most models of experimental amyloidosis, including golden Syrian hamsters (Mesocricetus auratus), involve massive and repeated inflammatory stimulation; however, the model of spontaneous amyloidosis with aging in female, but not male, Syrian hamsters permits analysis of amyloidogenic factors in the absence of inflammation. Another genus, the Armenian hamster (Cricetulus migratorius), differs from Syrian hamsters both in gender-specific serum amyloid P expression and susceptibility to AA amyloidosis. In this study, we describe novel SAA molecules in the Syrian hamster in the presence and absence of inflammation. We demonstrate that, based on isoelectric separation, the Syrian hamster SAA proteins can be separated into two broad subfamilies. Plasma SAA concentration in female Syrian hamsters increases spontaneously with age, and fragments of a basic SAA isotype expressed both hepatically and extrahepatically are selectively deposited as AA fibrils. After inflammatory stimulation, the patterns of SAA gene expression in Syrian and Armenian hamsters differ. In Syrian hamsters, both hepatic SAA mRNA and the high density lipoprotein apoSAA content increase approximately 1000-fold; in Armenian hamsters, hepatic SAA mRNA is limited in quantity and different in structure; and although plasma SAA proteins increase three- to fivefold, apoSAA is not detectable in high density lipoprotein. The results suggest that regulation and site of precursor production as well as precursor structure influence AA amyloidogenesis in these two hamster genera.

摘要

淀粉样蛋白A(AA)淀粉样变性在动物界广泛存在。包括以下几个因素:1)前体产生;2)前体结构;3)前体降解;4)前体/产物与五聚体血清淀粉样蛋白P的相互作用都与淀粉样蛋白生成有关,但导致AA纤维形成和沉积的确切事件顺序仍不清楚。大多数实验性淀粉样变性模型,包括金黄仓鼠(Mesocricetus auratus),都涉及大量且反复的炎症刺激;然而,雌性叙利亚仓鼠而非雄性叙利亚仓鼠随年龄增长出现的自发性淀粉样变性模型,允许在无炎症的情况下分析淀粉样蛋白生成因子。另一个属,亚美尼亚仓鼠(Cricetulus migratorius),在性别特异性血清淀粉样蛋白P表达和对AA淀粉样变性的易感性方面与叙利亚仓鼠不同。在本研究中,我们描述了叙利亚仓鼠在有炎症和无炎症情况下的新型血清淀粉样蛋白A(SAA)分子。我们证明,基于等电分离,叙利亚仓鼠SAA蛋白可分为两个广泛的亚家族。雌性叙利亚仓鼠的血浆SAA浓度随年龄自发增加,肝脏和肝外表达的一种碱性SAA同种型的片段被选择性地沉积为AA纤维。炎症刺激后,叙利亚仓鼠和亚美尼亚仓鼠的SAA基因表达模式不同。在叙利亚仓鼠中,肝脏SAA mRNA和高密度脂蛋白载脂蛋白SAA(apoSAA)含量均增加约1000倍;在亚美尼亚仓鼠中,肝脏SAA mRNA数量有限且结构不同;尽管血浆SAA蛋白增加了三到五倍,但在高密度脂蛋白中未检测到apoSAA。结果表明,前体产生的调节和部位以及前体结构影响这两个仓鼠属中的AA淀粉样蛋白生成。

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