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用BAPTA-AM装载神经元会激活xbp1加工过程,这表明内质网应激被诱导。

Loading neurons with BAPTA-AM activates xbp1 processing indicative of induction of endoplasmic reticulum stress.

作者信息

Paschen Wulf, Hotop Svenja, Aufenberg Christoph

机构信息

Department of Experimental Neurology, Max-Planck-Institute for Neurological Research, Gleuelerstr 50, Cologne 50931, Köln, Germany.

出版信息

Cell Calcium. 2003 Feb;33(2):83-9. doi: 10.1016/s0143-4160(02)00195-1.

Abstract

Loading cells with the calcium chelator BAPTA-AM is an analytical tool which has been used to suppress a rise in cytoplasmic calcium activity under various experimental conditions and thus, to evaluate the role of elevated cytoplasmic calcium levels in the process under investigation. BAPTA-AM may, however, not only have an isolated effect on cytoplasmic processes but also on functions of other subcellular compartments such as the endoplasmic reticulum (ER). Under conditions associated with ER dysfunction, the unfolded protein response is activated which is characterized by suppression of translation and processing of xbp1 mRNA, resulting in activation of the expression of genes coding for ER stress proteins. To investigate whether BAPTA-AM causes ER stress, primary neuronal cell cultures were loaded with varying amounts of BAPTA-AM. Exposure of cells to BAPTA-AM induced a marked rise in processed xbp1 mRNA levels, correlating with exposure times and BAPTA-AM concentrations in the medium used for loading. The increase in processed xbp1 mRNA was associated with suppression of protein synthesis and induction of cell injury. The results of this study indicate that loading primary neuronal cell cultures with BAPTA-AM activates xbp1 processing, implying that this calcium chelator does not have an isolated effect on cytoplasmic calcium activity but also an affect on ER function.

摘要

用钙螯合剂BAPTA-AM处理细胞是一种分析工具,已被用于在各种实验条件下抑制细胞质钙活性的升高,从而评估细胞质钙水平升高在研究过程中的作用。然而,BAPTA-AM不仅可能对细胞质过程有单独的影响,还可能对其他亚细胞区室如内质网(ER)的功能产生影响。在与内质网功能障碍相关的条件下,未折叠蛋白反应被激活,其特征是xbp1 mRNA的翻译和加工受到抑制,导致编码内质网应激蛋白的基因表达激活。为了研究BAPTA-AM是否会引起内质网应激,将不同量的BAPTA-AM加载到原代神经元细胞培养物中。细胞暴露于BAPTA-AM会导致加工后的xbp1 mRNA水平显著升高,这与加载所用培养基中的暴露时间和BAPTA-AM浓度相关。加工后的xbp1 mRNA的增加与蛋白质合成的抑制和细胞损伤的诱导有关。这项研究的结果表明,用BAPTA-AM处理原代神经元细胞培养物会激活xbp1的加工,这意味着这种钙螯合剂不仅对细胞质钙活性有单独的影响,还会对内质网功能产生影响。

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