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Auto-regulation of Secretory Flux by Sensing and Responding to the Folded Cargo Protein Load in the Endoplasmic Reticulum.
Subramanian, Advait; Capalbo, Anita; Iyengar, Namrata Ravi; Rizzo, Riccardo; di Campli, Antonella; Di Martino, Rosaria; Lo Monte, Matteo; Beccari, Andrea R; Yerudkar, Amol; Del Vecchio, Carmen; Glielmo, Luigi; Turacchio, Gabriele; Pirozzi, Marinella; Kim, Sang Geon; Henklein, Petra; Cancino, Jorge; Parashuraman, Seetharaman; Diviani, Dario; Fanelli, Francesca; Sallese, Michele; Luini, Alberto.
Afiliação
  • Subramanian A; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy. Electronic address: a.subramanian@ibp.cnr.it.
  • Capalbo A; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy.
  • Iyengar NR; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy.
  • Rizzo R; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy.
  • di Campli A; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy; Department of Medical, Oral and Biotechnological Sciences and CeSI-MeT, Center for Research on Ageing and Translational Medicine, "G. d'Annunzio" University of Chieti-Pescara, Chieti, Italy.
  • Di Martino R; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy.
  • Lo Monte M; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy.
  • Beccari AR; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy; Dompé Farmaceutici SpA, Milan, Italy.
  • Yerudkar A; Department of Engineering, Universitá degli Studi del Sannio, Benevento, Italy.
  • Del Vecchio C; Department of Engineering, Universitá degli Studi del Sannio, Benevento, Italy.
  • Glielmo L; Department of Engineering, Universitá degli Studi del Sannio, Benevento, Italy.
  • Turacchio G; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy.
  • Pirozzi M; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy.
  • Kim SG; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, South Korea.
  • Henklein P; Institut fur Biochemie, Charite Universitätsmedizin, Berlin, Germany.
  • Cancino J; Centro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, Santiago 7510157, Chile.
  • Parashuraman S; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy.
  • Diviani D; Université de Lausanne, Département de Pharmacologie et Toxicologie, Rue du Bugnon 27, 1011 Lausanne, Switzerland.
  • Fanelli F; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Sallese M; Department of Medical, Oral and Biotechnological Sciences and CeSI-MeT, Center for Research on Ageing and Translational Medicine, "G. d'Annunzio" University of Chieti-Pescara, Chieti, Italy.
  • Luini A; Institute of Protein Biochemistry (IBP), Italian National Research Council (CNR), Napoli, Italy. Electronic address: a.luini@ibp.cnr.it.
Cell ; 176(6): 1461-1476.e23, 2019 03 07.
Article em En | MEDLINE | ID: mdl-30849374
ABSTRACT
Maintaining the optimal performance of cell processes and organelles is the task of auto-regulatory systems. Here we describe an auto-regulatory device that helps to maintain homeostasis of the endoplasmic reticulum (ER) by adjusting the secretory flux to the cargo load. The cargo-recruiting subunit of the coatomer protein II (COPII) coat, Sec24, doubles as a sensor of folded cargo and, upon cargo binding, acts as a guanine nucleotide exchange factor to activate the signaling protein Gα12 at the ER exit sites (ERESs). This step, in turn, activates a complex signaling network that activates and coordinates the ER export machinery and attenuates proteins synthesis, thus preventing large fluctuations of folded and potentially active cargo that could be harmful to the cell or the organism. We call this mechanism AREX (autoregulation of ER export) and expect that its identification will aid our understanding of human physiology and diseases that develop from secretory dysfunction.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte Vesicular / Retículo Endoplasmático Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte Vesicular / Retículo Endoplasmático Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article