Membrane cycling after the excess retrieval mode of rapid endocytosis in mouse chromaffin cells

Aim: After exocytosis, neuroendocrine cells and neurones keep constant the plasma membrane and the releasable vesicle pools by performing endocytosis and vesicular cycling. Patch-clamp capacitance measurements on chromaffin cells showed that strong Ca +2 entry activates excess retrieval: a rapid end...

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Autor principal: Perez Bay, A.E
Otros Autores: Belingheri, A.V, Álvarez, Y.D, Marengo, F.D
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2012
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024 7 |2 cas  |a calcium, 14092-94-5, 7440-70-2; dextran, 87915-38-6, 9014-78-2; potassium, 7440-09-7; protein kinase C, 141436-78-4; Calcium, 7440-70-2; Calcium Channel Blockers; Calcium Channels, L-Type; Cholinergic Agonists; FM1 43; Fluorescent Dyes; Potassium, 7440-09-7; Protein Kinase C, 2.7.11.13; Protein Kinase Inhibitors; Pyridinium Compounds; Quaternary Ammonium Compounds 
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100 1 |a Perez Bay, A.E. 
245 1 0 |a Membrane cycling after the excess retrieval mode of rapid endocytosis in mouse chromaffin cells 
260 |c 2012 
270 1 0 |m Marengo, F.D.; Laboratorio de Fisiología y Biología Molecular, Universidad de Buenos Aires, Departamento de Fisiología y Biología Molecular y Celular, Instituto de Fisiologia Biologia Molecular y Neurociencias, Facultad de Ciencias Exactas y Naturales, Ciudad Universitaria, Pabellón II, 2o piso, Buenos Aires CP: 1428, Argentina; email: fernando@fbmc.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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504 |a Perez Bay, A.E., Ibanez, L.I., Marengo, F.D., Rapid recovery of releasable vesicles and formation of nonreleasable endosomes follow intense exocytosis in chromaffin cells (2007) Am J Physiol Cell Physiol, 293, pp. C1509-C1522 
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504 |a Smith, C., Neher, E., Multiple forms of endocytosis in bovine adrenal chromaffin cells (1997) J Cell Biol, 139, pp. 885-894 
504 |a Wu, W., Wu, L.G., Rapid bulk endocytosis and its kinetics of fission pore closure at a central synapse (2007) Proc Natl Acad Sci USA, 104, pp. 10234-10239 
504 |a ZhuGe, R., DeCrescenzo, V., Sorrentino, V., Lai, F.A., Tuft, R.A., Lifshitz, L.M., Lemos, J.R., Walsh Jr., J.V., Syntillas release Ca 2+ at a site different from the microdomain where exocytosis occurs in mouse chromaffin cells (2006) Biophys J, 90, pp. 2027-2037 
520 3 |a Aim: After exocytosis, neuroendocrine cells and neurones keep constant the plasma membrane and the releasable vesicle pools by performing endocytosis and vesicular cycling. Patch-clamp capacitance measurements on chromaffin cells showed that strong Ca +2 entry activates excess retrieval: a rapid endocytosis process that retrieves more membrane than the one fused by preceding exocytosis. The main purpose of the present experiments was to study the recycling pathway that follows excess retrieval, which is unknown. Methods: Membrane recycling after exocytosis-endocytosis can be studied by fluorescence imaging assays with FM1-43 (Perez Bay et al. Am J Physiol Cell Physiol 2007; 293, C1509). In this work, we used this assay in combination with fluorescent dextrans and specific organelle-targeted antibodies to study the membrane recycling after excess retrieval in mouse chromaffin cells. Results: Excess retrieval was observed after the application of high-K + or cholinergic agonists during 15 or 30s in the presence of FM1-43. We found that the excess retrieval membrane pool (defined as endocytosis-exocytosis) was associated with the generation of a non-releasable fraction of membrane (up to 30% of plasma membrane surface) colocalizing with the lysosomal compartment. The excess retrieval membrane pool followed a saturable cytosolic Ca 2+ dependency, and it was suppressed by inhibitors of L-type Ca 2+ channels, endoplasmic reticulum Ca 2+ release and PKC. Conclusion: Excess retrieval is not associated with the cycling of releasable vesicles, but it is related to the formation of non-releasable endosomes. This process is activated by a concerted contribution of Ca 2+ entry through L-channels and Ca 2+ release from endoplasmic reticulum. © 2011 The Authors. Acta Physiologica © 2011 Scandinavian Physiological Society.  |l eng 
593 |a Laboratorio de Fisiología y Biología Molecular, Universidad de Buenos Aires, Departamento de Fisiología y Biología Molecular y Celular, Inst. de Fisiologia Biologia Molecular y Neurociencias CONICET, Fac. de Ciencias Exactas y Naturales, Buenos Aires, Argentina 
593 |a Department of Ophthalmology, Dyson Vision Research Institute, Weill Medical College, Cornell University, New York, NY, United States 
690 1 0 |a CALCIUM SIGNAL 
690 1 0 |a ENDOCYTOSIS 
690 1 0 |a EXOCYTOSIS 
690 1 0 |a FM1-43 
690 1 0 |a MEMBRANE CYCLING 
690 1 0 |a CALCIUM 
690 1 0 |a CALCIUM CHANNEL L TYPE 
690 1 0 |a CHOLINERGIC RECEPTOR STIMULATING AGENT 
690 1 0 |a DEXTRAN 
690 1 0 |a FM 143 
690 1 0 |a POTASSIUM 
690 1 0 |a PROTEIN KINASE C 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ARTICLE 
690 1 0 |a CALCIUM CELL LEVEL 
690 1 0 |a CALCIUM SIGNALING 
690 1 0 |a CALCIUM TRANSPORT 
690 1 0 |a CELL ASSAY 
690 1 0 |a CELL MEMBRANE 
690 1 0 |a CELL SURFACE 
690 1 0 |a CELLULAR DISTRIBUTION 
690 1 0 |a CHROMAFFIN CELL 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a CYTOSOL 
690 1 0 |a ENDOCYTOSIS 
690 1 0 |a ENDOPLASMIC RETICULUM 
690 1 0 |a EXOCYTOSIS 
690 1 0 |a FLUORESCENCE IMAGING 
690 1 0 |a LYSOSOME 
690 1 0 |a MOUSE 
690 1 0 |a NONHUMAN 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a RECYCLING 
690 1 0 |a ANIMALS 
690 1 0 |a CALCIUM 
690 1 0 |a CALCIUM CHANNEL BLOCKERS 
690 1 0 |a CALCIUM CHANNELS, L-TYPE 
690 1 0 |a CALCIUM SIGNALING 
690 1 0 |a CELL MEMBRANE 
690 1 0 |a CHOLINERGIC AGONISTS 
690 1 0 |a CHROMAFFIN CELLS 
690 1 0 |a ELECTRIC CAPACITANCE 
690 1 0 |a ENDOCYTOSIS 
690 1 0 |a ENDOPLASMIC RETICULUM 
690 1 0 |a ENDOSOMES 
690 1 0 |a EXOCYTOSIS 
690 1 0 |a FLUORESCENT DYES 
690 1 0 |a MEMBRANE FUSION 
690 1 0 |a MEMBRANE POTENTIALS 
690 1 0 |a MICE 
690 1 0 |a MICROSCOPY, FLUORESCENCE 
690 1 0 |a PATCH-CLAMP TECHNIQUES 
690 1 0 |a POTASSIUM 
690 1 0 |a PROTEIN KINASE C 
690 1 0 |a PROTEIN KINASE INHIBITORS 
690 1 0 |a PYRIDINIUM COMPOUNDS 
690 1 0 |a QUATERNARY AMMONIUM COMPOUNDS 
690 1 0 |a TIME FACTORS 
653 0 0 |a fm 143 
700 1 |a Belingheri, A.V. 
700 1 |a Álvarez, Y.D. 
700 1 |a Marengo, F.D. 
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