ORALS
SESSION: OxidativeThuPM2-R5
| Intl. Symp. on Oxidative Stress for Sustainable Development of Human Beings |
Thu Oct, 24 2019 / Room: Zeus (55/Mezz. F) | |
Session Chairs: Alexander Oleinick; Harry van Goor; Session Monitor: TBA |
16:20: [OxidativeThuPM210]
Theoretical Aspects of Reactive Oxygen/Nitrogen Species Homeostasis inside Macrophages during Phagocytosis Monitored at Nanoelectrodes Alexander
Oleinick1 ; Xin-wei
Zhang
2 ;
Irina
Svir3 ;
Christian
Amatore4 ; Wei-hua
Huang
5 ;
1CNRS-ENS-SU UMR 8640 PASTEUR, CNRS, Paris, France;
2Key Laboratory of Analytical Chemistry for Biology and Medicine, College of Chemistry and Molecular Sciences, Wuhan, China;
3Ecole Normale Superieure, Department Chemistry, PARIS, France;
4CNRS & PSL, French Acad. of Sci. and Xiamen University, Paris, France;
5Wuhan University, Wuhan, China;
Paper Id: 322
[Abstract] Traffic of the lipid-enclosed compartments (vesicles, endosomes, phagosomes etc.) within the cell is extremely important for sustaining cell life and allowing the cell to perform its function. These lipid bilayer bound organelles deliver their cargo through bilayer fusion with the other organelles or with the plasma membrane. In the case when the release of the cargo molecule is controlled only by diffusion, we have shown earlier for the case of vesicular exocytosis that emptying of such organelles occurs exponentially and the rate of the exponential decay is controlled by the size of the fusion pore [1]. The generality of the assumptions made for model derivation, as well as for laws underlying this model, suggest that the assumptions can be applied to a vast variety of cases. This can be done independently if organelles fuse with another part like the cellular membrane or electrode (like in vesicle impact electrochemical cytometry), etc. Moreover, being able to describe mass transport of the cargo molecules inside or out of the organelle allow one to characterize various physicochemical processes occurring within the organelle [2].
In particular, relevantly adapted models were applied to the case of the detection with the platinized carbon nanoelectrode of the reactive oxygen/nitrogen species (ROS/RNS) produced by macrophages inside their phagolysosomes (more on the experiment will be presented in Prof. Wei-Hua Huang's talk) [3]. Modelling the oxidation and mass transport of the ROS/RNS towards the nanoelectrode and comparison with experimental data evidenced <u>for the first time</u> that the consumption of ROS/RNS by their oxidation at the nanoelectrode surface stimulates the production of significant ROS/RNS amounts inside phagolysosomes, i.e., proved the very existence of a ROS/RNS homeostasis during phagocytosis. The homeostatic production rates of ROS/RNS inside individual phagolysosomes were quantified by employing the developed theory [3]. These results allowed measuring the long-time postulated ROS/RNS homeostasis within the phagolysosome, its kinetics and its efficiency. ROS/RNS concentrations may then be maintained at sufficiently high levels to sustain proper pathogen digestion rates without endangering the macrophage internal structures [3].
References:
1. A. Oleinick, I. Svir, C. Amatore. Proc. R. Soc. A, 473, 2017, 20160684.\n2. A. Oleinick, I. Svir, W.-H. Huang, C. Amatore, in preparation.\n3. X.-W. Zhang, A. Oleinick, H. Jiang, Q.-L. Liao, Q.-F. Qiu, I. Svir, Y.-L. Liu, C. Amatore, W.-H. Huang. Angew. Chem. Ind. Ed., 58, 2019, 7753-7756.
SESSION: OxidativeThuPM2-R5
| Intl. Symp. on Oxidative Stress for Sustainable Development of Human Beings |
Thu Oct, 24 2019 / Room: Zeus (55/Mezz. F) | |
Session Chairs: Alexander Oleinick; Harry van Goor; Session Monitor: TBA |
16:45: [OxidativeThuPM211]
Electrochemical Monitoring of ROS/RNS Homeostasis Within Individual Phagolysosomes Inside Single Macrophages Wei-hua
Huang1 ;
1Wuhan University, Wuhan, China;
Paper Id: 321
[Abstract] Reactive Oxygen/Nitrogen Species (ROS/RNS) produced by macrophages inside their phagolysosomes are closely related to immunity and inflammation by being involved in the removal of pathogens, altered cells, etc. The existence of a homeostatic mechanism regulating the ROS/RNS amounts inside phagolyso¬somes has been invoked to account for the efficiency of this crucial process, but this could never be unambiguously documented. Here, intracellular electrochemical analysis with platinized nanowires electrodes (Pt-NWEs) allowed monitoring of ROS/RNS effluxes with sub-millisecond resolution from individual phagolysosomes. These randomly impacted onto the electrode and were inserted inside a living macrophage. This evidenced for the first time that the consumption of ROS/RNS by their oxidation at the nanoelectrode surface stimulates the production of significant ROS/RNS amounts inside phagolysosomes. These results established the existence of the long-time postulated ROS/RNS homeostasis and allowed to quantify its kinetics and efficiency. ROS/RNS concentrations may then be maintained at sufficiently high levels for sustaining proper pathogen digestion rates without endangering the macrophage internal structures.
References:
[1] X. W. Zhang, Q. F. Qiu, H. Jiang, F. L. Zhang, Y. L. Liu, C. Amatore, W. H. Huang, Angew. Chem. Int. Ed. 56 (2017) 12997-13000.
[2] X. W. Zhang, A. Oleinick, H. Jiang, Q. L. Liao, Q. F. Qiu, I. Svir, Y. L. Liu, C. Amatore, W. H. Huang, Angew. Chem. Int. Ed. 58 (2019) 7753-7756.