The Gárdos Channel and Piezo1 Revisited: Comparison between Reticulocytes and Mature Red Blood Cells

Author:

Petkova-Kirova Polina12ORCID,Murciano Nicoletta34ORCID,Iacono Giulia56ORCID,Jansen Julia47,Simionato Greta78,Qiao Min47ORCID,van der Zwaan Carmen56,Rotordam Maria Giustina3,John Thomas7ORCID,Hertz Laura47,Hoogendijk Arjan J.56,Becker Nadine3,Wagner Christian79ORCID,von Lindern Marieke56ORCID,Egee Stephane1011ORCID,van den Akker Emile56ORCID,Kaestner Lars47ORCID

Affiliation:

1. Institute of Neurobiology, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria

2. Department of Biochemistry, Saarland University, 66123 Saarbrücken, Germany

3. Nanion Technologies, 80339 Munich, Germany

4. Theoretical Medicine and Biosciences, Campus University Hospital, Saarland University, 66421 Homburg, Germany

5. Department of Hematopoiesis, Sanquin Research, 1066 CX Amsterdam, The Netherlands

6. Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, 1007 MB Amsterdam, The Netherlands

7. Department of Experimental Physics, Saarland University, 66123 Saarbrücken, Germany

8. Department of Experimental Surgery, Campus University Hospital, Saarland University, 66421 Homburg, Germany

9. Physics and Materials Science Research Unit, University of Luxembourg, L-1511 Luxembourg, Luxembourg

10. Biological Station Roscoff, Sorbonne University, CNRS, UMR8227 LBI2M, F-29680 Roscoff, France

11. Laboratory of Excellence GR-Ex, F-75015 Paris, France

Abstract

The Gárdos channel (KCNN4) and Piezo1 are the best-known ion channels in the red blood cell (RBC) membrane. Nevertheless, the quantitative electrophysiological behavior of RBCs and its heterogeneity are still not completely understood. Here, we use state-of-the-art biochemical methods to probe for the abundance of the channels in RBCs. Furthermore, we utilize automated patch clamp, based on planar chips, to compare the activity of the two channels in reticulocytes and mature RBCs. In addition to this characterization, we performed membrane potential measurements to demonstrate the effect of channel activity and interplay on the RBC properties. Both the Gárdos channel and Piezo1, albeit their average copy number of activatable channels per cell is in the single-digit range, can be detected through transcriptome analysis of reticulocytes. Proteomics analysis of reticulocytes and mature RBCs could only detect Piezo1 but not the Gárdos channel. Furthermore, they can be reliably measured in the whole-cell configuration of the patch clamp method. While for the Gárdos channel, the activity in terms of ion currents is higher in reticulocytes compared to mature RBCs, for Piezo1, the tendency is the opposite. While the interplay between Piezo1 and Gárdos channel cannot be followed using the patch clamp measurements, it could be proved based on membrane potential measurements in populations of intact RBCs. We discuss the Gárdos channel and Piezo1 abundance, interdependencies and interactions in the context of their proposed physiological and pathophysiological functions, which are the passing of small constrictions, e.g., in the spleen, and their active participation in blood clot formation and thrombosis.

Funder

European Community in Marie Skłodowska-Curie

Publisher

MDPI AG

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