Electrochemical Monitoring of Single Cell Secretion: Vesicular Exocytosis and Oxidative Stress

Physiological stimuli evoke two forms of endocytosis in bovine chromaffin cells

Chan, S., & Smith, C. L. (2001) · The Journal of Physiology · doi:10.1113/jphysiol.2001.012838 · Cited by 50

Regulation of the NADPH-oxidase complex of phagocytic leukocytes. Recent insights from structural biology, molecular genetics, and microscopy

Robinson, J. M., Ohira, T., & Badwey, J. A. (2004) · Histochemistry and Cell Biology · doi:10.1007/s00418-004-0672-2 · Cited by 49

Compound exocytosis in voltage-clamped mouse pancreatic β-cells revealed by carbon fibre amperometry

Bokvist, K., Holmqvist, M., Gromada, J., & Rorsman, P. (2000) · Pfl�gers Archiv European Journal of Physiology · doi:10.1007/s004240050987 · Cited by 48

Enhancement of the Dense-Core Vesicle Secretory Cycle by Glucocorticoid Differentiation of PC12 Cells: Characteristics of Rapid Exocytosis and Endocytosis

Elhamdani, A., Brown, M. E., Artalejo, C. R., & Palfrey, H. C. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02495.2000 · Cited by 48

Regulation of the Fusion Pore Conductance during Exocytosis by Cyclin-dependent Kinase 5

Barclay, J. W., Aldea, M., Craig, T. J., Morgan, A., & Burgoyne, R. D. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m406670200 · Cited by 47

Relationship between amperometric pre-spike feet and secretion granule composition in Chromaffin cells: An overview

Amatore, C. A., Arbault, S., Bonifas, I., Guille‐Collignon, M., Lemaître, F., & Verchier, Y. (2007) · Biophysical Chemistry · doi:10.1016/j.bpc.2007.05.018 · Cited by 47

Requirements for the identification of dense-core granules

Meldolesi, J., Chieregatti, E., & Malosio, M. L. (2003) · Trends in Cell Biology · doi:10.1016/j.tcb.2003.11.006 · Cited by 46

Amplification of the Inflammatory Cellular Redox State by Human Immunodeficiency Virus Type 1-Immunosuppressive Tat and gp160 Proteins

Lachgar, A., Šojić, N., Arbault, S., Bruce, D., Sarasin, A. R., Amatore, C. A., Bizzini, B., Zagury, D., & Vuillaume, M. (1999) · Journal of Virology · doi:10.1128/jvi.73.2.1447-1452.1999 · Cited by 44

Activity-Dependent Nitric Oxide Concentration Dynamics in the Laterodorsal Tegmental Nucleus In Vitro

Leonard, C. S., Michaelis, E. K., & Mitchell, K. M. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.5.2159 · Cited by 44

Adrenaline Release by Chromaffin Cells: Constrained Swelling of the Vesicle Matrix Leads to Full Fusion

Amatore, C. A., Bouret, Y., Travis, E. R., & Wightman, R. M. (2000) · Angewandte Chemie International Edition · Cited by 43

Short-Term Changes in the Ca2+-Exocytosis Relationship during Repetitive Pulse Protocols in Bovine Adrenal Chromaffin Cells

Engisch, K. L., Chernevskaya, N. I., & Nowycky, M. C. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-23-09010.1997 · Cited by 42

Exocytosis: Using Amperometry to Study Presynaptic Mechanisms of Neurotoxicity

Westerink, R. H. S. (2003) · NeuroToxicology · doi:10.1016/j.neuro.2003.10.006 · Cited by 41

Controlled on-chip stimulation of quantal catecholamine release from chromaffin cells using photolysis of caged Ca 2+ on transparent indium-tin-oxide microchip electrodes

Chen, X., Gao, Y., Hossain, M., Gangopadhyay, S., & Gillis, K. D. (2007) · Lab on a Chip · doi:10.1039/b715308m · Cited by 41

Micro-Enzyme Electrode Prepared on Platinized Platinum

Ikariyama, Y., Yamauchi, S., Yukiashi, T., & Ushioda, H. (1987) · Analytical Letters · doi:10.1080/00032718708066322 · Cited by 40

Dopamine levels of two classes of vesicles are differentially depleted by amphetamine

Anderson, B. B., Chen, G., Gutman, D. A., & Ewing, A. G. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00040-7 · Cited by 39

Ion interaction at the pore of Lc‐type Ca2+ channel is sufficient to mediate depolarization‐induced exocytosis

Lerner, I., Trus, M., Cohen, R., Yizhar, O., Nussinovitch, I., & Atlas, D. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03709.x · Cited by 39

Temperature-dependent differences between readily releasable and reserve pool vesicles in chromaffin cells

Haynes, C. L., Siff, L. N., & Wightman, R. M. (2007) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2007.03.013 · Cited by 39

Nitric oxide reduces blood pressure in the nucleus tractus solitarius: a real time electrochemical study

Wu, W. C., Wang, Y., Kao, L. S., Tang, F., & Chai, C. Y. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00737-7 · Cited by 38

Fusion pore regulation of transmitter release

Fernández-Peruchena, C. M., Navas, S. J., Montes, M. Á., & de Toledo, G. Á. (2005) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.12.037 · Cited by 38

Nicotine-evoked nitric oxide release in the rat hippocampal slice

Smith, D. A., Hoffman, A. F., David, D., Adams, C. E., & Gerhardt, G. A. (1998) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00725-3 · Cited by 37

Quantitation of epinephrine and norepinephrine secretion from individual adrenal medullary cells by microcolumn high-performance liquid chromatography

Cooper, B. R., Wightman, R. M., & Jorgenson, J. W. (1994) · Journal of Chromatography B Biomedical Sciences and Applications · doi:10.1016/0378-4347(93)e0423-n · Cited by 36

Role of DNA Excision Repair Gene Defects in the Etiology of Cancer

Ford, J. M., & Hanawalt, P. C. (1997) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-60505-5_5 · Cited by 35

Electroanalysis of Metabolic Flux from Single Cells in Simple Picoliter-Volume Microsystems

Yasukawa, T., Glidle, A., Cooper, J. M., & Matsue, T. (2002) · Analytical Chemistry · doi:10.1021/ac025836u · Cited by 35

Chemical profiles and monitoring dynamics at an individual nerve cell in Planorbis corneus with electrochemical detection

Anderson, B. B., & Ewing, A. G. (1999) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/s0731-7085(98)00088-0 · Cited by 35

Superoxide generation from constitutive nitric oxide synthase in astrocytes in vitro regulates extracellular nitric oxide availability

Tolias, C. M., McNeil, C. J., Kazlauskaite, J., & Hillhouse, E. W. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00146-4 · Cited by 35

Quantal release of free radicals during exocytosis of phagosomes

Di, A., Krupa, B., Bindokas, V. P., Chen, Y., Brown, M. E., Palfrey, H. C., Naren, A. P., Kirk, K. L., & Nelson, D. J. (2002) · Nature Cell Biology · doi:10.1038/ncb771 · Cited by 35

Calcium-dependent and ouabain-resistant oxygen consumption in the rat neurohypophysis

Shibuki, K. (1989) · Brain Research · doi:10.1016/0006-8993(89)90944-x · Cited by 33

Control of membrane fusion dynamics during regulated exocytosis

Burgoyne, R. D., Fisher, R. J., Graham, M. E., Haynes, L. P., & Morgan, A. (2001) · Biochemical Society Transactions · doi:10.1042/bst0290467 · Cited by 33

Calcium dependence of action potential-induced endocytosis in chromaffin cells

Chan, S., Chow, R. H.-P., & Smith, C. L. (2003) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-002-0966-y · Cited by 32

Vesicular Ca2+-induced secretion promoted by intracellular pH-gradient disruption

Haynes, C. L., Buhler, L. A., & Wightman, R. M. (2006) · Biophysical Chemistry · doi:10.1016/j.bpc.2006.04.005 · Cited by 32

Vesicular Exocytosis under Hypotonic Conditions Shows Two Distinct Populations of Dense Core Vesicles in Bovine Chromaffin Cells

Amatore, C. A., Arbault, S., Bonifas, I., Lemaître, F., & Verchier, Y. (2007) · ChemPhysChem · doi:10.1002/cphc.200600607 · Cited by 32

Peroxynitrite/Nitric Oxide Balance in Ischemia/Reperfusion Injury‐Nanomedical Approach

Kubant, R., Malinski, C., Burewicz, A., & Maliñski, T. (2006) · Electroanalysis · doi:10.1002/elan.200503436 · Cited by 32

Relationship between fusion pore opening and release during mast cell exocytosis studied with patch amperometry

Tabares, L., Lindau, M., & de Toledo, G. Á. (2003) · Biochemical Society Transactions · doi:10.1042/bst0310837 · Cited by 31

Hydralazine Reduces the Quantal Size of Secretory Events by Displacement of Catecholamines From Adrenomedullary Chromaffin Secretory Vesicles

Machado, J. D., Gómez, J. F., Betancor, G., Camacho, M., Brioso, M. A., & Borges, R. (2002) · Circulation Research · doi:10.1161/01.res.0000039530.30495.6f · Cited by 31

Pattern of Ca2+ increase determines the type of secretory mechanism activated in dog pancreatic duct epithelial cells

Jung, S., Kim, K., Hille, B., Nguyen, T. D., & Koh, D. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.114876 · Cited by 30

Acid‐evoked quantal catecholamine secretion from rat phaeochromocytoma cells and its interaction with hypoxia‐evoked secretion

Taylor, S. C., Roberts, M. L., & Peers, C. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.0765n.x · Cited by 28

The effect of transfection with Botulinum neurotoxin C1 light chain on exocytosis measured in cell populations and by single-cell amperometry in PC12 cells

Fisher, R. J., & Burgoyne, R. D. (1999) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240050842 · Cited by 27

Electrochemical detection of nitric oxide production in perfused pig coronary artery: comparison of the performances of two electrochemical sensors

Villeneuve, N., Fethi Bedioui, A., Voituriez, K., Avaro, S., & Vilaine, J. P. (1998) · Journal of Pharmacological and Toxicological Methods · doi:10.1016/s1056-8719(98)00043-4 · Cited by 27

Multiple classes of catecholamine vesicles observed during exocytosis from the Planorbis cell body

Chen, G., & Ewing, A. G. (1995) · Brain Research · doi:10.1016/0006-8993(95)00989-9 · Cited by 27

Three Distinct Ca2+Influx Pathways Couple Acetylcholine Receptor Activation to Catecholamine Secretion from PC12 Cells

Taylor, S. C., & Peers, C. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0751583.x · Cited by 27

Amperometry and cyclic voltammetry of tyrosine and tryptophan‐containing oligopeptides at carbon fiber microelectrodes applied to single cell analysis

Paras, C. D., & Kennedy, R. T. (1997) · Electroanalysis · doi:10.1002/elan.1140090303 · Cited by 27

Differential regulation of multiple populations of granules in rat adrenal chromaffin cells by culture duration and cyclic AMP

Tang, K. S., Tse, A., & Tse, F. W. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02944.x · Cited by 26

Sodium—Calcium Exchange Affects Local Calcium Signal Decay and the Rate of Exocytotic Secretion in Single Chromaffin Cells

Tang, Y. M., Travis, E. R., Wightman, R. M., & Schneider, A. S. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.740702.x · Cited by 26

Localized Exocytosis Detected by Spatially Resolved Amperometry in Single Pancreatic β-Cells

Paras, C. D., Qian, W., Lakey, J. R. T., Tan, W., & Kennedy, R. T. (2000) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:33:3:227 · Cited by 25

Life imaging of peroxynitrite in rat microglial and astroglial cells: Role of superoxide and antioxidants

Possel, H., Noack, H., Keilhoff, G., & Wolf, G. L. (2002) · Glia · doi:10.1002/glia.10066 · Cited by 25

Demonstration of two distributions of vesicle radius in the dopamine neuron of Planorbis corneus from electrochemical data

Anderson, B. B., Chen, G., Gutman, D. A., & Ewing, A. G. (1999) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(99)00024-2 · Cited by 24

Ageing changes the cellular basis of the “fight-or-flight” response in human adrenal chromaffin cells

Elhamdani, A., Palfrey, C., & Artalejo, C. R. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00275-5 · Cited by 23

Comparison of cytosolic Ca2+ and exocytosis responses from single rat and bovine chromaffin cells

Finnegan, J. M., Borges, R., & Wightman, R. M. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00459-9 · Cited by 22

Calculation of transmitter concentration in individual PC12 cell vesicles with electrochemical data and a distribution of vesicle size obtained by electron microscopy

Anderson, B. B., Zerby, S. E., & Ewing, A. G. (1999) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(99)00023-0 · Cited by 22

Temperature dependence of release of vesicular content in bovine chromaffin cells

Walker, A., Glavinović, M. I., & Trifaró, J. M. (1996) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240050212 · Cited by 22

[36] Peroxynitrite studied by stopped-flow spectroscopy

Kissner, R., Beckman, J. S., & Koppenol, W. H. (1999) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(99)01098-8 · Cited by 21

Nitric Oxide and Peroxynitrite Affect Differently Acetylcholine Release, Choline Acetyltransferase Activity, Synthesis, and Compartmentation of Newly Formed Acetylcholine inTorpedo marmorataSynaptosomes

Gaudry-Talarmain, Y. M., Moulian, N., Meunier, F. A., Blanchard, B., Angaut‐Petit, D., Faille, L., & Ducrocq, C. (1997) · Nitric Oxide · doi:10.1006/niox.1997.0141 · Cited by 21

A rapid exocytosis mode in chromaffin cells with a neuronal phenotype

Ardiles, Á. O., Maripillán, J., Lagos, V. L., Toro, R., Mora, I. G., Villarroel, L., Alés, E., Borges, R., & Cárdenas, A. M. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04080.x · Cited by 21

Stimulus-Dependent Alterations in Quantal Neurotransmitter Release

Grabner, C. P., & Fox, A. P. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00017.2006 · Cited by 19

A New Ultramicrosensor for Nitric Oxide Based on Electropolymerized Film of Nickel Salen

Mao, L., Tian, Y., Shi, G., et al. (1998) · Analytical Letters · doi:10.1080/00032719808005280 · Cited by 18

Monoamine release by neurons of a primitive nervous system: an amperometric study

Gillis, M., & Anctil, M. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00172.x · Cited by 16

The Nature and Efficiency of Neurotransmitter Exocytosis also Depend on Physicochemical Parameters

Amatore, C. A., Arbault, S., Guille‐Collignon, M., & Lemaître, F. (2007) · ChemPhysChem · doi:10.1002/cphc.200700225 · Cited by 16

On the Chemical and Electrochemical One-Electron Reduction of Peroxynitrous Acid

Kurz, C., Zeng, X., Hannemann, S., Kissner, R., & Koppenol, W. H. (2005) · The Journal of Physical Chemistry A · doi:10.1021/jp046123d · Cited by 15

Physical techniques for the study of exocytosis in isolated cells

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Vasoactive intestinal peptide potentiates and directly stimulates catecholamine secretion from rat adrenal chromaffin cells

Anděrová, M., Duchêne, A. D., Barbara, J., & Takeda, K. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00856-7 · Cited by 15

Phenylarsine oxide inhibits ex vivo HIV-1 expression

Arbault, S., Edeas, M. A., Legrand-Poels, S., Šojić, N., Amatore, C. A., Piette, J. G., Best‐Belpomme, M., Lindenbaum, A., & Vuillaume, M. (1997) · Biomedicine & Pharmacotherapy · doi:10.1016/s0753-3322(97)82321-9 · Cited by 14

Electrochemical detection of nitroso-arginine as an intermediate between N-hydroxy-arginine and citrulline. An in vitro versus in vivo study using microcarbon electrodes in neuronal nitric oxide synthase and mice brain

Meulemans, A. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01548-2 · Cited by 12

A brain nitric oxide synthase study in the rat: production of a nitroso-compound NA and absence of nitric oxide synthesis

Meulemans, A. (2002) · Neuroscience Letters · doi:10.1016/s0304-3940(02)00055-1 · Cited by 11

Microdomains of High Calcium Are Not Required for Exocytosis in Rbl-2h3 Mucosal Mast Cells

Mahmoud, S. F., & Fewtrell, C. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.2.339 · Cited by 11

Morphological and functional characterization of beige mouse adrenomedullary secretory vesicles

Borges, R., Jaén, R., Freire, F. N., Gómez, J. F., Villafruela, C., & Yanes, E. C. (2001) · Cell and Tissue Research · doi:10.1007/s004410000320 · Cited by 6

A simple way to build a grinder for carbon-fibre electrodes for amperometry or voltammetry

Borges, R., Díaz‐Vera, J., Camacho, M., & Machado, J. D. (2005) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-005-1380-z · Cited by 5

Production of NA by endothelial NO-synthase: An in vitro versus in vivo study

Meulemans, A. (2005) · Comptes Rendus Biologies · doi:10.1016/j.crvi.2004.12.002 · Cited by 2

ROS production in phagocytes: Why, when, and where?

Dupré-Crochet, S., Erard, M., & Nüβe, O. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.1012544 · Cited by 467

Conductive Polymer-Coated Carbon Nanotubes To Construct Stretchable and Transparent Electrochemical Sensors

Jin, Z.-H., Liu, Y.-L., Chen, J.-J., Cai, S.-L., Xu, J.-Q., & Huang, W.-H. (2017) · Analytical Chemistry · doi:10.1021/acs.analchem.6b04616 · Cited by 116

Stretchable Electrochemical Sensors for Cell and Tissue Detection

Liu, Y., & Huang, W. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202007754 · Cited by 105

A Stretchable Electrochemical Sensor for Inducing and Monitoring Cell Mechanotransduction in Real Time

Liu, Y., Qin, Y., Jin, Z., Hu, X., Chen, M., Liu, R., Amatore, C., & Huang, W. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201705215 · Cited by 89

STIM-Orai Channels and Reactive Oxygen Species in the Tumor Microenvironment

Frisch, J., Angenendt, A., Hoth, M., Prates Roma, L., & Lis, A. (2019) · Cancers · doi:10.3390/cancers11040457 · Cited by 68