The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes

被引:43
|
作者
Castonguay, Jan [1 ]
Orth, Joachim H. C. [1 ]
Mueller, Thomas [1 ]
Sleman, Faten [1 ]
Grimm, Christian [1 ,5 ,6 ]
Wahl-Schott, Christian [5 ,6 ]
Biel, Martin [5 ,6 ]
Mallmann, Robert Theodor [1 ]
Bildl, Wolfgang [2 ]
Schulte, Uwe [2 ,3 ,4 ]
Klugbauer, Norbert [1 ]
机构
[1] Albert Ludwigs Univ, Fac Med, Inst Expt & Clin Pharmacol & Toxicol, Albertstr 25, D-79104 Freiburg, Germany
[2] Albert Ludwigs Univ, Fac Med, Inst Physiol 2, Hermann Herder Str 7, D-79104 Freiburg, Germany
[3] Logopharm GmbH, Schlossstr 14, D-79232 March Buchheim, Germany
[4] Ctr Biol Signaling Studies BIOSS, Schanzlestr 18, D-79104 Freiburg, Germany
[5] Ludwig Maximilians Univ Munchen, Ctr Drug Res, Dept Pharm, Munich, Germany
[6] Ludwig Maximilians Univ Munchen, CIPSM, Munich, Germany
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
PASTEURELLA-MULTOCIDA TOXIN; CALCIUM-RELEASE; CHOLERA-TOXIN; ION CHANNELS; NAADP; LOCALIZATION; ACTIVATION; ROLES; GLYCOSPHINGOLIPIDS; GTPASE;
D O I
10.1038/s41598-017-10607-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Two-pore channels (TPCs) are localized in endo-lysosomal compartments and assumed to play an important role for vesicular fusion and endosomal trafficking. Recently, it has been shown that both TPC1 and 2 were required for host cell entry and pathogenicity of Ebola viruses. Here, we investigate the cellular function of TPC1 using protein toxins as model substrates for distinct endosomal processing routes. Toxin uptake and activation through early endosomes but not processing through other compartments were reduced in TPC1 knockout cells. Detailed co-localization studies with subcellular markers confirmed predominant localization of TPC1 to early and recycling endosomes. Proteomic analysis of native TPC1 channels finally identified direct interaction with a distinct set of syntaxins involved in fusion of intracellular vesicles. Together, our results demonstrate a general role of TPC1 for uptake and processing of proteins in early and recycling endosomes, likely by providing high local Ca2+ concentrations required for SNARE-mediated vesicle fusion.
引用
收藏
页数:15
相关论文
共 42 条
  • [21] Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) Induces Intracellular Ca2+ Release through the Two-Pore Channel TPC1 in Metastatic Colorectal Cancer Cells
    Faris, Pawan
    Pellavio, Giorgia
    Ferulli, Federica
    Di Nezza, Francesca
    Shekha, Mudhir
    Lim, Dmitry
    Maestri, Marcello
    Guerra, Germano
    Ambrosone, Luigi
    Pedrazzoli, Paolo
    Laforenza, Umberto
    Montagna, Daniela
    Moccia, Francesco
    CANCERS, 2019, 11 (04)
  • [22] Functional analysis of the two pore channel TPC1: Conventional black lipid bilayer and multichannel setup
    Mueller, T.
    Zaitseva, E.
    Baaken, G.
    Mallmann, R.
    Schulte, U.
    Klugbauer, N.
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2016, 389 (01) : S45 - S45
  • [23] mTORC1 controls lysosomal Ca2+ release through the two-pore channel TPC2
    Ogunbayo, Oluseye A.
    Duan, Jingxian
    Xiong, Jian
    Wang, Qiaochu
    Feng, Xinghua
    Ma, Jianjie
    Zhu, Michael X.
    Evans, A. Mark
    SCIENCE SIGNALING, 2018, 11 (525)
  • [24] Nicotinic acid adenine dinucleotide phosphate activates two-pore channel TPC1 to mediate lysosomal Ca2+release in endothelial colony-forming cells
    Moccia, Francesco
    Zuccolo, Estella
    Di Nezza, Francesca
    Pellavio, Giorgia
    Faris, Pawan S.
    Negri, Sharon
    De Luca, Antonio
    Laforenza, Umberto
    Ambrosone, Luigi
    Rosti, Vittorio
    Guerra, Germano
    JOURNAL OF CELLULAR PHYSIOLOGY, 2021, 236 (01) : 688 - 705
  • [25] Membrane Potential Regulates Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) Dependence of the pH- and Ca2+- sensitive Organellar Two-pore Channel TPC1
    Rybalchenko, Volodymyr
    Ahuja, Malini
    Coblentz, Jessica
    Churamani, Dev
    Patel, Sandip
    Kiselyov, Krill
    Muallem, Shmuel
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (24) : 20407 - 20416
  • [26] Two-pore channel protein 1 contributes to NAADP triggered acrosome reaction in spermatozoa
    Arlt, E.
    Arndt, L.
    Breit, A.
    Wennemuth, G.
    Biel, M.
    Wahl, C.
    Gudermann, T.
    Klugbauer, N.
    Boekhoff, I.
    REPRODUCTION IN DOMESTIC ANIMALS, 2017, 52 : 6 - 7
  • [27] NAADP and the two-pore channel protein 1 participate in the acrosome reaction in mammalian spermatozoa
    Arndt, L.
    Arlt, E.
    Castonguay, J.
    Hassan, S.
    Zierler, S.
    Wennemuth, G.
    Breit, A.
    Biel, M.
    Wahl-Schott, C.
    Gudermann, T.
    Klugbauer, N.
    Boekhoff, I.
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2016, 389 (01) : S43 - S44
  • [28] NAADP and the two-pore channel protein 1 participate in the acrosome reaction in mammalian spermatozoa
    Arndt, Lilli
    Castonguay, Jan
    Arlt, Elisabeth
    Meyer, Dorke
    Hassan, Sami
    Borth, Heike
    Zierler, Susanna
    Wennemuth, Gunther
    Breit, Andreas
    Biel, Martin
    Wahl-Schott, Christian
    Gudermann, Thomas
    Klugbauer, Norbert
    Boekhoff, Ingrid
    MOLECULAR BIOLOGY OF THE CELL, 2014, 25 (06) : 948 - 964
  • [29] Application of bacterial protein toxins to TPC1 deficient cells reveals the role of two pore channels for intracellular endolysosomal trafficking processes
    Mallmann, R.
    Orth, J.
    Castonguay, J.
    Mueller, T.
    Klugbauer, N.
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2016, 389 (01) : S44 - S45
  • [30] Increased accumulation of cadmium and lead under Ca and Fe deficiency in Typha latifolia: A study of two pore channel (TPC1) gene responses
    Rodriguez-Hernandez, M. C.
    Bonifas, I.
    Alfaro-De la Torre, M. C.
    Flores-Flores, J. L.
    Banuelos-Hernandez, B.
    Patino-Rodriguez, O.
    ENVIRONMENTAL AND EXPERIMENTAL BOTANY, 2015, 115 : 38 - 48