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肌醇1,4,5-三磷酸受体定位于内核膜,这证明了肌醇1,4,5-三磷酸对核钙信号的调节作用。磷酸肌醇受体在内核膜和外核膜上的分布是离散的。

Inositol 1,4,5-trisphosphate receptor is located to the inner nuclear membrane vindicating regulation of nuclear calcium signaling by inositol 1,4,5-trisphosphate. Discrete distribution of inositol phosphate receptors to inner and outer nuclear membranes.

作者信息

Humbert J P, Matter N, Artault J C, Köppler P, Malviya A N

机构信息

Laboratoire de Neurobiologie Moléculaire des Interactions Cellulaires, Centre National de la Recherche Scientifique, Strasbourg, France.

出版信息

J Biol Chem. 1996 Jan 5;271(1):478-85. doi: 10.1074/jbc.271.1.478.

Abstract

Transient rise in nuclear calcium concentration is implicated in the regulation of events controlling gene expression. Mechanism by which calcium is transported to the nucleus is vehemently debated. Inositol 1,4,5-trisphosphate (InsP3) and inositol-1,3,4,5-tetrakisphosphate (InsP4) receptors have been located to the nucleus and their role in nuclear calcium signaling has been proposed. Outer nuclear membrane was separated from the inner membrane. The two membrane preparations were, as best as possible, devoid of cross contamination as attested by marker enzyme activity, Western blotting with antilamin antibody, and electron microscopy. InsP4 receptor and Ca(2+)-ATPase were located to the outer nuclear membrane. InsP3 receptor was located to the inner nuclear membrane. ATP or InsP4 induced nuclear calcium uptake. External free calcium concentration, in the medium bathing the nuclei, determined the choice for ATP or InsP4-mediated calcium transport. We present a mechanistic model for nuclear calcium transport. According to this model, calcium can reach the nucleus envelope either by the action of ATP or InsP4. However, the calcium release from the nucleus envelope to the nucleoplasm is mediated by InsP3 through the activation of InsP3 receptor, which is located to the inner nuclear membrane. The action of InsP3 in this process was instantaneous and transient and was sensitive to heparin.

摘要

核钙浓度的短暂升高与控制基因表达的事件调节有关。钙被转运至细胞核的机制一直存在激烈争论。肌醇1,4,5-三磷酸(InsP3)和肌醇-1,3,4,5-四磷酸(InsP4)受体已定位至细胞核,并且有人提出了它们在核钙信号传导中的作用。外核膜与内核膜分离。通过标记酶活性、抗层粘连蛋白抗体的蛋白质印迹法和电子显微镜证实,这两种膜制剂尽可能没有交叉污染。InsP4受体和Ca(2+)-ATP酶定位在外核膜上。InsP3受体定位在内核膜上。ATP或InsP4诱导核钙摄取。细胞核周围培养基中的细胞外游离钙浓度决定了是选择ATP还是InsP4介导的钙转运。我们提出了一个核钙转运的机制模型。根据这个模型,钙可以通过ATP或InsP4的作用到达核膜。然而,钙从核膜释放到核质是由InsP3通过激活位于内核膜上的InsP3受体介导的。InsP3在此过程中的作用是瞬时的和短暂的,并且对肝素敏感。

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