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异丙肾上腺素对大鼠腮腺中他汀类相关基因表达的下调作用。

Isoproterenol downregulation of statin-related gene expression in the rat parotid gland.

作者信息

Ann D K, Wechsler A, Lin H H, Wang E

机构信息

Department of Pharmacology, University of Minnesota, Medical School, Minneapolis 55455.

出版信息

J Cell Sci. 1991 Nov;100 ( Pt 3):641-7. doi: 10.1242/jcs.100.3.641.

Abstract

Statin, a 57 kilodalton (kDa) nuclear protein, is characteristically found in nonproliferating cells in culture as well as nondividing cells of a wide range of highly differentiated tissues. Moreover, cells in culture that are statin positive lose this statin expression when re-entering the cell-cycle traverse. In this work, statin expression was investigated in the parotid gland of untreated rats and those treated with isoproterenol (IPR), a proliferation-inducing catecholamine. Indirect immunofluorescence microscopy revealed specific nuclear staining with anti-statin monoclonal antibody (S-44) in the acinar and ducts cells of the untreated rats but significantly reduced in those induced with isoproterenol. To characterize the protein recognized by S-44, protein extracts from both tissues were immunoblotted and incubated with S-44. The antibody reacted specifically with a 48 kDa protein in the extract of the parotid glands from untreated rats while no reaction was detected in that of the proliferation-induced ones. These observations along with the result that a statin-like (S1) transcript is downregulated by isoproterenol in the parotid glands further support the notion that the disappearance of statin-related expression is associated with the IPR-induced proliferation in the rat parotid glands. The discrepancy between the apparent molecular mass of the protein identified by S-44 in nonproliferating parotid cells and that of statin originally found in fibroblasts, suggests that either a modified form of statin may be present in the parotid gland, or this 48 kDa protein may be a member of the nonproliferative statin-like family.

摘要

他汀蛋白是一种57千道尔顿(kDa)的核蛋白,其特征在于在培养的非增殖细胞以及广泛高度分化组织的非分裂细胞中被发现。此外,培养中呈他汀蛋白阳性的细胞在重新进入细胞周期进程时会失去这种他汀蛋白表达。在这项研究中,研究了未处理大鼠以及用异丙肾上腺素(IPR,一种诱导增殖的儿茶酚胺)处理的大鼠腮腺中的他汀蛋白表达。间接免疫荧光显微镜显示,未处理大鼠的腺泡细胞和导管细胞中用抗他汀蛋白单克隆抗体(S - 44)进行特异性核染色,但在用异丙肾上腺素诱导的大鼠中显著减少。为了鉴定被S - 44识别的蛋白质,对来自两种组织的蛋白质提取物进行免疫印迹并与S - 44孵育。该抗体与未处理大鼠腮腺提取物中的一种48 kDa蛋白质特异性反应,而在增殖诱导大鼠的提取物中未检测到反应。这些观察结果以及腮腺中一种类他汀(S1)转录本被异丙肾上腺素下调的结果进一步支持了这样的观点,即他汀蛋白相关表达的消失与大鼠腮腺中IPR诱导的增殖有关。S - 44在非增殖腮腺细胞中鉴定出的蛋白质表观分子量与最初在成纤维细胞中发现的他汀蛋白分子量之间的差异,表明要么腮腺中可能存在他汀蛋白的修饰形式,要么这种48 kDa蛋白质可能是非增殖性类他汀家族的成员。

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