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Titel: Red Blood Cell Membrane Conductance in Hereditary Haemolytic Anaemias
VerfasserIn: Petkova-Kirova, Polina
Hertz, Laura
Danielczok, Jens
Huisjes, Rick
Makhro, Asya
Bogdanova, Anna
Mañú-Pereira, Maria Del Mar
Vives Corrons, Joan-Lluis
van Wijk, Richard
Kaestner, Lars
Sprache: Englisch
Titel: Frontiers in Physiology
Bandnummer: 10
Verlag/Plattform: Frontiers
Erscheinungsjahr: 2019
Freie Schlagwörter: haemolytic anemia
patch-clamp
electrophysiology
hereditary spherocytosis
hereditary xerocytosis
DDC-Sachgruppe: 610 Medizin, Gesundheit
Dokumenttyp: Journalartikel / Zeitschriftenartikel
Abstract: Congenital haemolytic anaemias are inherited disorders caused by red blood cell membrane and cytoskeletal protein defects, deviant hemoglobin synthesis and metabolic enzyme deficiencies. In many cases, although the causing mutation might be known, the pathophysiology and the connection between the particular mutation and the symptoms of the disease are not completely understood. Thus effective treatment is lagging behind. As in many cases abnormal red blood cell cation content and cation leaks go along with the disease, by direct electrophysiological measurements of the general conductance of red blood cells, we aimed to assess if changes in the membrane conductance could be a possible cause. We recorded whole-cell currents from 29 patients with different types of congenital haemolytic anaemias: 14 with hereditary spherocytosis due to mutations in α-spectrin, β-spectrin, ankyrin and band 3 protein; 6 patients with hereditary xerocytosis due to mutations in Piezo1; 6 patients with enzymatic disorders (3 patients with glucose-6-phosphate dehydrogenase deficiency, 1 patient with pyruvate kinase deficiency, 1 patient with glutamate-cysteine ligase deficiency and 1 patient with glutathione reductase deficiency), 1 patient with β-thalassemia and 2 patients, carriers of several mutations and a complex genotype. While the patients with β-thalassemia and metabolic enzyme deficiencies showed no changes in their membrane conductance, the patients with hereditary spherocytosis and hereditary xerocytosis showed largely variable results depending on the underlying mutation.
DOI der Erstveröffentlichung: 10.3389/fphys.2019.00386
URL der Erstveröffentlichung: https://www.frontiersin.org/articles/10.3389/fphys.2019.00386
Link zu diesem Datensatz: urn:nbn:de:bsz:291--ds-402053
hdl:20.500.11880/36163
http://dx.doi.org/10.22028/D291-40205
ISSN: 1664-042X
Datum des Eintrags: 26-Jul-2023
Fakultät: M - Medizinische Fakultät
Fachrichtung: M - Anatomie und Zellbiologie
Professur: M - Keiner Professur zugeordnet
Sammlung:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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