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V-ATP酶/雷帕霉素靶蛋白信号通路调节巨膜蛋白介导的顶端内吞作用。

V-ATPase/mTOR signaling regulates megalin-mediated apical endocytosis.

作者信息

Gleixner Eva Maria, Canaud Guillaume, Hermle Tobias, Guida Maria Clara, Kretz Oliver, Helmstädter Martin, Huber Tobias B, Eimer Stefan, Terzi Fabiola, Simons Matias

机构信息

Center for Systems Biology (ZBSA), University of Freiburg, Habsburgerstrasse 49, 79104 Freiburg, Germany; Renal Division, University Hospital Freiburg, Hugstetter Strasse 55, 79106 Freiburg, Germany.

INSERM U845, Centre de Recherche "Croissance et Signalisation," Université Paris Descartes, Sorbonne Paris Cité, Hôpital Necker-Enfants Malades, 75015 Paris, France.

出版信息

Cell Rep. 2014 Jul 10;8(1):10-9. doi: 10.1016/j.celrep.2014.05.035. Epub 2014 Jun 19.

Abstract

mTOR kinase is a master growth regulator that can be stimulated by multiple signals, including amino acids and the lysosomal small GTPase Rheb. Recent studies have proposed an important role for the V-ATPase in the sensing of amino acids in the lysosomal lumen. Using the Drosophila wing as a model epithelium, we show here that the V-ATPase is required for Rheb-dependent epithelial growth. We further uncover a positive feedback loop for the control of apical protein uptake that depends on V-ATPase/mTOR signaling. This feedback loop includes Rheb-dependent transcriptional regulation of the multiligand receptor Megalin, which itself is required for Rheb-induced endocytosis. In addition, we provide evidence that long-term mTOR inhibition with rapamycin in mice causes reduction of Megalin levels and proteinuria in the proximal tubular epithelium of the kidney. Thus, our findings unravel a homeostatic mechanism that allows epithelial cells to promote protein uptake under normal conditions and to prevent uptake in lysosomal stress conditions.

摘要

mTOR激酶是一种主要的生长调节因子,可被多种信号激活,包括氨基酸和溶酶体小GTP酶Rheb。最近的研究表明,V-ATP酶在溶酶体腔内氨基酸感知中发挥重要作用。我们以果蝇翅膀作为模型上皮组织,在此表明V-ATP酶是Rheb依赖的上皮生长所必需的。我们进一步揭示了一个用于控制顶端蛋白摄取的正反馈回路,该回路依赖于V-ATP酶/mTOR信号传导。这个反馈回路包括Rheb依赖的多配体受体巨蛋白的转录调控,而巨蛋白本身是Rheb诱导的内吞作用所必需的。此外,我们提供的证据表明,在小鼠中用雷帕霉素长期抑制mTOR会导致肾脏近端小管上皮中巨蛋白水平降低和蛋白尿。因此,我们的研究结果揭示了一种稳态机制,该机制使上皮细胞能够在正常条件下促进蛋白摄取,并在溶酶体应激条件下阻止摄取。

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