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离子转运蛋白 NKCC1 通过抑制 mTORC1 将细胞体积与细胞质量调节联系起来。

The Ion Transporter NKCC1 Links Cell Volume to Cell Mass Regulation by Suppressing mTORC1.

机构信息

Program in Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; Biochemistry Department, University of Toronto, Toronto, ON M5S 1A8, Canada.

Program in Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.

出版信息

Cell Rep. 2019 May 7;27(6):1886-1896.e6. doi: 10.1016/j.celrep.2019.04.034.

Abstract

mTORC1 regulates cellular growth and is activated by growth factors and by essential amino acids such as Leu. Leu enters cells via the Leu transporter LAT1-4F2hc (LAT1). Here we show that the Na/K/2Cl cotransporter NKCC1 (SLC12A2), a known regulator of cell volume, is present in complex with LAT1. We further show that NKCC1 depletion or deletion enhances LAT1 activity, as well as activation of Akt and Erk, leading to activation of mTORC1 in cells, colonic organoids, and mouse colon. Moreover, NKCC1 depletion reduces intracellular Na concentration and cell volume (size) and mass and stimulates cell proliferation. NKCC1, therefore, suppresses mTORC1 by inhibiting its key activating signaling pathways. Importantly, by linking ion transport and cell volume regulation to mTORC1 function, NKCC1 provides a long-sought link connecting cell volume (size) to cell mass regulation.

摘要

mTORC1 调节细胞生长,受生长因子和亮氨酸等必需氨基酸激活。亮氨酸通过亮氨酸转运体 LAT1-4F2hc(LAT1)进入细胞。在这里,我们表明,已知调节细胞体积的 Na+/K+/2Cl-共转运体 NKCC1(SLC12A2)与 LAT1 形成复合物。我们进一步表明,NKCC1 的耗竭或缺失增强了 LAT1 的活性,以及 Akt 和 Erk 的激活,导致细胞、结肠类器官和小鼠结肠中 mTORC1 的激活。此外,NKCC1 的耗竭降低了细胞内 Na+浓度和细胞体积(大小)和质量,并刺激细胞增殖。因此,NKCC1 通过抑制其关键激活信号通路来抑制 mTORC1。重要的是,通过将离子转运和细胞体积调节与 mTORC1 功能联系起来,NKCC1 提供了一个长期以来寻求的将细胞体积(大小)与细胞质量调节联系起来的途径。

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