Szczegóły publikacji

Opis bibliograficzny

Spectroscopic signature of red blood cells in a D-galactose-induced accelerated aging model / A. Blat, Tetiana Stepanenko, Katarzyna Bułat, A. WAJDA, Jakub Dybas, Tasnim Mohaissen, Fatih Celal Alcicek, Ewa Szczesny-Malysiak, Kamilla Malek, Andrzej Fedorowicz, Katarzyna M. Marzec // International Journal of Molecular Sciences [Dokument elektroniczny]. — Czasopismo elektroniczne ; ISSN 1422-0067. — 2021 — vol. 22 iss. 5 art. no. 2660, s. 1–15. — Wymagania systemowe: Adobe Reader. — Bibliogr. s. 13–15, Abstr. — Publikacja dostępna online od: 2021-03-06. — A. Wajda – dod. afiliacja: Jagiellonian Center for Experimental Therapeutics, Jagiellonian University; T. Stepanenko – afiliacja: Jagiellonian University; K. Bułat, K. Marzec – afiliacja: Jagiellonian Center for Experimental Therapeutics, Jagiellonian University

Autorzy (11)

  • Blat Aneta
  • Stepanenko Tetiana
  • Bułat Katarzyna
  • AGHWajda Aleksandra Anna
  • Dybas Jakub
  • Mohaissen Tasnim
  • Alcicek Fatih Celal
  • Szczęsny-Małysiak Ewa
  • Malek Kamilla
  • Fedorowicz A.
  • Marzec Katarzyna M.

Słowa kluczowe

ATRRaman spectroscopyvibrational spectroscopyRBCsFourier transform infrared spectroscopyD-galactose-induced accelerated aging mouse modelred blood cellsattenuated total reflectanceRBC membranesFTIRaging

Dane bibliometryczne

ID BaDAP133077
Data dodania do BaDAP2021-03-15
Tekst źródłowyURL
DOI10.3390/ijms22052660
Rok publikacji2021
Typ publikacjiartykuł w czasopiśmie
Otwarty dostęptak
Creative Commons
Czasopismo/seriaInternational Journal of Molecular Sciences

Abstract

This work presents a semi-quantitative spectroscopic approach, including FTIR–ATR and Raman spectroscopies, for the biochemical analysis of red blood cells (RBCs) supported by the biochemical, morphological and rheological reference techniques. This multi-modal approach provided the description of the RBC alterations at the molecular level in a model of accelerated aging induced by administration of D-galactose (D-gal), in comparison to natural aging. Such an approach allowed to conclude that most age-related biochemical RBC membrane changes (a decrease in lipid unsaturation and the level of phospholipids, or an increase in acyl chain shortening) as well as alterations in the morphological parameters and RBC deformability are well reflected in the D-gal model of accelerated aging. Similarly, as in natural aging, a decrease in LDL level in blood plasma and no changes in the fraction of glucose, creatinine, total cholesterol, HDL, iron, or triglycerides were observed during the course of accelerated aging. Contrary to natural aging, the D-gal model led to an increase in cholesterol esters and the fraction of total esterified lipids in RBC membranes, and evoked significant changes in the secondary structure of the membrane proteins. Moreover, a significant decrease in the phosphorous level of blood plasma was specific for the D-gal model. On the other hand, natural aging induced stronger changes in the secondary structures of the proteins of the RBCs’ interior. This work proves that research on the aging mechanism, especially in circulation-related diseases, should employ the D-gal model with caution. Nonetheless, the D-gal model enables to imitate age-related rheological alterations in RBCs, although they are partially derived from different changes observed in the RBC membrane at the molecular level.

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