Preview

General Reanimatology

Advanced search

Comparative Assessment of Hemin-Induced Alterations in Red Blood Cells Using Light Microscopy and Atomic Force Microscopy

https://doi.org/10.15360/1813-9779-2026-5-2724

Abstract

Aim of the study: to compare the capabilities of light microscopy and atomic force microscopy (AFM) in assessing the morphological features of red blood cell (RBC) damage.

Materials and Methods. The study used blood from three healthy male donors with a mean age of 36 ± 5 years. RBCs were incubated with a hemin solution for 60 minutes. After incubation, blood smears were prepared. Morphological analysis was performed using an Olympus CX41 light microscope. The RBC topography was assessed using AFM on an NTEGRA BIO instrument in semi-contact mode. The distribution of morphological forms, cell diameter, and cell height were analyzed.

Results. A predominance of discocytes was observed in the control group, using both methods (light microscopy — 94 ± 2 %, AFM — 94 ± 1 %). After exposure to hemin 96 ± 2 % of the cells lost their central pallor and were classified as planocytes according to light microscopy. However, AFM revealed that these cells were spheroechinocytes (98 ± 1 %), characterized by a decrease in diameter from 7.6 ± 0.6 μm to 5.9 ± 0.4 μm (p = 0.008), an increase in height from 356 ± 22 nm to 737 ± 148 nm (p = 0.047), and the presence of multiple protrusions on the membrane.

Conclusion. Light microscopy reveals the loss of central pallor but does not allow for verification of the true three-dimensional shape of the damaged cells. AFM is necessary to refine the morphological classification and to quantitatively assess height and diameter. Thus, light microscopy is suitable for initial screening, while AFM is suitable for detailed assessment of RBC morphological alterations. 

About the Authors

E. A. Sherstyukova
V. A. Negovsky Research Institute of General Reanimatology, Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Ministry of Education and Science of Russia
Russian Federation

Ekaterina A. Sherstyukova

25 Petrovka Str., Bldg. 2, 107031 Moscow



V. A. Sergunova
V. A. Negovsky Research Institute of General Reanimatology, Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Ministry of Education and Science of Russia
Russian Federation

Viktoria A. Sergunova

25 Petrovka Str., Bldg. 2, 107031 Moscow



References

1. Ghosh B., Agarwal K. Viewing life without labels under optical microscopes. Commun Biol. 2023; 6 (1): 559. DOI: 10.1038/s42003-023-04934-8. PMID: 37231084.

2. Balasubramanian H., Hobson C.M., Chew T.-L., Aaron J.S. Imagining the future of optical microscopy: everything, everywhere, all at once. Commun Biol. 2023; 6 (1): 1096. DOI: 10.1038/s42003-023-05468-9. PMID: 37898673.

3. Noble C.A., Biesemier A.P., McClees S.F., Alhussain A.M., Helms S.E., Brodell R.T. The history of the microscope reflects advances in science and medicine. Semin Diagn Pathol. 2025; 42 (2): 150831. DOI: 10.1053/j.semdp.2024.01.002. PMID: 38627186.

4. Robertson L.A. Antoni van Leeuwenhoek 1723-2023: a review to commemorate Van Leeuwenhoek’s death, 300 years ago: for submission to Antonie van Leeuwenhoek journal of microbiology. Antonie Van Leeuwenhoek. 2023; 116 (10): 919–935. DOI: 10.1007/s10482-023-01859-4. PMID: 37525002.

5. Somssich M. A short history of plant light microscopy. Curr. Protoc. 2022; 2 (10): e577. DOI: 10.1002/cpz1.577. PMID: 36200878.

6. Hou W., Wei Y. Evaluating the resolution of conventional optical microscopes through point spread function measurement. iScience. 2023; 26 (10): 107976. DOI: 10.1016/j.isci.2023.107976. PMID: 37822495.

7. Jayakumar N., Ahluwalia B.S. From superior contrast to super resolution label free optical microscopy. Npj Imaging. 2025; 3 (1): 1. DOI: 10.1038/s44303-024-00064-w. PMID: 40604121.

8. Astratov V.N., Sahel Y.B., Eldar Y.C., Huang L., Ozcan A., Zheludev N., Zhao J., et al. Roadmap on label-free super-resolution imaging. Laser Photonics Rev. 2023; 17 (12): 2200029. DOI: 10.1002/lpor.202200029. PMID: 38883699.

9. Hsieh H.-C., Han Q., Brenes D., Bishop K.W., Wang R., Wang Y., Poudel C., et al. Imaging 3D cell cultures with optical microscopy. Nat Methods. 2025; 22 (6): 1167–1190. DOI: 10.1038/s41592-025-02647-w. PMID: 40247123.

10. Shaked N.T., Boppart S.A., Wang L.V., Popp J. Label-free biomedical optical imaging. Nat Photonics. 2023; 17 (12): 1031–1041. DOI: 10.1038/s41566-023-01299-6. PMID: 38523771.

11. Wang Y., Zhang X., Xu J., Sun X., Zhao X., Li H., Liu Y., et al. The development of microscopic imaging technology and its application in micro- and nanotechnology. Front Chem. 2022; 10: 931169. DOI: 10.3389/fchem.2022.931169. PMID: 35864864.

12. Cuny A.P., Schlottmann F.P., Ewald J.C., Pelet S., Schmoller K.M. Live cell microscopy: from image to insight. Biophys Rev (Melville). 2022; 3 (2): 021302. DOI: 10.1063/5.0082799. PMID: 38505412.

13. Bourn M.D., Daly L.F., Huggett J.F., Braybrook J., Rivera J.F. Evaluation of image analysis tools for the measurement of cellular morphology. Front Cell Dev Biol. 2025; 13: 1572212. DOI: 10.3389/fcell.2025.1572212. PMID: 40443732.

14. Persano F., Parodi A., Pallaeva T., Kolesova E., Zamyatnin A.A., Pokrovsky V.S., De Matteis V., et al. Atomic force microscopy: a versatile tool in cancer research. Cancers (Basel). 2025; 17 (5): 858. DOI: 10.3390/cancers17050858. PMID: 40075706.

15. Sergunova V., Leesment S., Kozlov A., Inozemtsev V., Platitsina P., Lyapunova S., Onufrievich A., et al. Investigation of red blood cells by atomic force microscopy. Sensors (Basel). 2022; 22 (5): 2055. DOI: 10.3390/s22052055. PMID: 35271203.

16. Garcia R., Tejedor J.R. Advances in nanomechanical property mapping by atomic force microscopy. Nanoscale Adv. 2025; 7 (20): 6286–6307. DOI: 10.1039/D5NA00702J. PMID: 40880595.

17. Efremov Y.M., Suter D.M., Timashev P.S., Raman A. 3D nanomechanical mapping of subcellular and sub-nuclear structures of living cells by multi-harmonic AFM with long-tip microcantilevers. Sci Rep. 2022; 12 (1): 529. DOI: 10.1038/s41598-021-04443-w. PMID: 35017598.

18. Yang Q., Chen D., Li C., Liu R., Wang X. Mechanism of hypoxia-induced damage to the mechanical property in human erythrocytes-band 3 phosphorylation and sulfhydryl oxidation of membrane proteins. Front Physiol. 2024; 15: 1399154. DOI: 10.3389/fphys.2024.1399154. PMID: 38706947.

19. Dinarelli S., Longo G., Francioso A., Mosca L., Girasole M. Mechanotransduction boosts the aging effects in human erythrocytes submitted to mechanical stimulation. Int J Mol Sci. 2022; 23 (17): 10180. DOI: 10.3390/ijms231710180. PMID: 36077573.

20. He L., Yu Z., Zhu J., Cao X., Song X. Nanostructure and nanomechanics of Prorocentrum donghaiense and their changes under nitrogen limitation by atomic force microscopy. Front Mar Sci. 2022; 9: 874888. DOI: 10.3389/fmars.2022.874888.

21. Mikhailova D.M., Skverchinskaya E., Sudnitsyna J., Butov K.R., Koltsova E.M., Mindukshev I.V., Gambaryan S. Hematin- and hemin-induced spherization and hemolysis of human erythrocytes are independent of extracellular calcium concentration. Cells. 2024; 13 (6): 554. DOI: 10.3390/cells13060554. PMID: 38534398.

22. Georgiou-Siafis S.K., Samiotaki M.K., Demopoulos V.J., Panayotou G., Tsiftsoglou A.S. Glutathione-hemin/hematin adduct formation to disintegrate cytotoxic oxidant hemin/hematin in human K562 cells and red blood cells’ hemolysates: impact of glutathione on the hemolytic disorders and homeostasis. Antioxidants (Basel). 2022; 11 (10): 1959. DOI: 10.3390/antiox11101959. PMID: 36290682.

23. Guo Y., Zhao H., Lin Z., Ye T., Xu D., Zeng Q. Heme in cardiovascular diseases: a ubiquitous dangerous molecule worthy of vigilance. Front Cell Dev Biol. 2021; 9: 781839. DOI: 10.3389/fcell.2021.781839. PMID: 35127704.

24. Wiatr M., Hadzhieva M., Lecerf M., Noé R., Justesen S., Lacroix-Desmazes S., Dragon-Durey M.-A. et al. Hyperoxidized species of heme have a potent capacity to induce autoreactivity of human IgG antibodies. Int J Mol Sci. 2023; 24 (4): 3416. DOI: 10.3390/ijms24043416. PMID: 36834827.

25. Giri R.P., Chowdhury S., Mukhopadhyay M.K., Chakrabarti A., Sanyal M.K. Ganglioside GM1 drives hemin and protoporphyrin adsorption in phospholipid membranes: a structural study. J Phys Chem B. 2024; 128 (11): 2745–2754. DOI: 10.1021/acs.jpcb.3c08239. PMID: 38447189.

26. Moroz V.V., Kozlova E.K., Chernysh A.M., Gudkova O.E., Bushueva A.V. Hemin induced changes in the red blood cell membrane structure. General Reanimatology = Obshchaya Reanimatologiya. 2012; 8 (6): 5–10. (in Russ.&Eng.). DOI: 10.15360/1813-9779-2012-6-5.

27. Sherstyukova E.A., Inozemtsev V.A., Kozlov A.P., Gudkova O.E., Sergunova V.A. Atomic force microscopy in the assessment of erythrocyte membranes mechanical properties with exposure to various physicochemical agents. Almanac of Clinical Medicine = Almanakh Klinicheskoy Meditsiny. 2021; 49 (6): 427–434. (in Russ.). DOI: 10.18786/2072-0505-2021-49-059.

28. Kozlova E., Sergunova V., Sherstyukova E., Gudkova O., Kozlov A., Inozemtsev V., Lyapunova S. et al. Topological relationships cytoskeleton-membrane nanosurface-morphology as a basic mechanism of total disorders of RBC structures. Int J Mol Sci. 2022; 23 (4): 2045. DOI: 10.3390/ijms23042045. PMID: 35216154.

29. Giri A., Tamgadge S. Red blood cells in health and disease. J Microsc Ultrastruct. 2025; 13 (3): 130-136. DOI: 10.4103/jmau.jmau_70_23. PMID: 41059161.

30. Strijkova-Kenderova V., Todinova S., Andreeva T., Bogdanova D., Langari A., Danailova A., Krumova S., et al. Morphometry and stiffness of red blood cells-signatures of neurodegenerative diseases and aging. Int J Mol Sci. 2021; 23 (1): 227. DOI: 10.3390/ijms23010227. PMID: 35008653.

31. Buys A.V., Van Rooy M.J., Soma P., Van Papendorp D., Lipinski B., Pretorius E. Changes in red blood cell membrane structure in type 2 diabetes: a scanning electron and atomic force microscopy study. Cardiovasc Diabetol. 2013; 12: 25. DOI: 10.1186/1475-2840-12-25. PMID: 23356738.

32. AlSalhi M.S., Devanesan S., AlZahrani K.E., AlShebly M., Al-Qahtani F., Farhat K., Masilamani V. Impact of diabetes mellitus on human erythrocytes: atomic force microscopy and spectral investigations. Int J Environ Res Public Health. 2018; 15 (11): 2368. DOI: 10.3390/ijerph15112368. PMID: 30373127.

33. Tyrrell L., Rose G., Shukri A., Kahwash S.B. Morphologic changes in red blood cells: an illustrated review of clinically important light microscopic findings. Malays J Pathol. 2021; 43 (2): 219–239. PMID: 34448787.

34. Rey-Barroso L., Roldán M., Burgos-Fernández F.J., Isola I., Ruiz Llobet A., Gassiot S., Sarrate E. et al. Membrane protein detection and morphological analysis of red blood cells in hereditary spherocytosis by confocal laser scanning microscopy. Microsc Microanal. 2023; 29 (2): 777–785. DOI: 10.1093/micmic/ozac055. PMID: 37749743.

35. Rahman S., Azam B., Khan S.U., Awais M., Ali I., Ul Hussen Khan R.J. Automatic identification of abnormal blood smear images using color and morphology variation of RBCS and central pallor. Comput Med Imaging Graph. 2021; 87: 101813. DOI: 10.1016/j.compmedimag.2020.101813. PMID: 33279759.

36. Su S., Zhao J., Ly T.H. Scanning probe microscopies for characterizations of 2D materials. Small Methods. 2024; 8 (13): 2400211. DOI: 10.1002/smtd.202400211.

37. Longo G., Dinarelli S., Collacchi F., Girasole M. Comparing nanomechanical properties and membrane roughness along the aging of human erythrocytes. Methods Protoc. 2025; 8 (4): 86. DOI: 10.3390/mps8040086. PMID: 40863736.

38. Kassa T., Jana S., Baek J.H., Alayash A.I. Impact of cold storage on the oxygenation and oxidation reactions of red blood cells. Front Physiol. 2024; 15: 1427094. DOI: 10.3389/fphys.2024.1427094. PMID: 39224206.

39. Liu S.C., Zhai S., Lawler J., Palek J. Hemin-mediated dissociation of erythrocyte membrane skeletal proteins. J Biol Chem. 1985; 260 (22): 12234–12239. DOI: 10.1016/S0021-9258 (17)39015-4. PMID: 4044594.

40. Li Y., Lu L., Li J. Topological structures and membrane nanostructures of erythrocytes after splenectomy in hereditary spherocytosis patients via atomic force microscopy. Cell Biochem Biophys. 2016; 74 (3): 365–371. DOI: 10.1007/s12013-016-0755-4. PMID: 27557951.

41. Demchenkov E.L., Nagdalian A.A., Budkevich R.O., Oboturova N.P., Okolelova A.I. Usage of atomic force microscopy for detection of the damaging effect of CdCl2 on red blood cells membrane. Ecotoxicol Environ Saf. 2021; 208: 111683. DOI: 10.1016/j.ecoenv.2020.111683. PMID: 33396015.

42. Giosheva I., Strijkova V., Komsa-Penkova R., Krumova S., Langari A., Danailova A., Taneva S.G. et al. Membrane lesions and reduced life span of red blood cells in preeclampsia as evidenced by atomic force microscopy. Int J Mol Sci. 2023; 24 (8): 7100. DOI: 10.3390/ijms24087100. PMID: 37108270.

43. Sinha A., Chu T.T.T., Dao M., Chandramohanadas R. Single-cell evaluation of red blood cell bio-mechanical and nano-structural alterations upon chemically induced oxidative stress. Sci Rep. 2015; 5: 9768. DOI: 10.1038/srep09768. PMID: 25950144.


Review

For citations:


Sherstyukova E.A., Sergunova V.A. Comparative Assessment of Hemin-Induced Alterations in Red Blood Cells Using Light Microscopy and Atomic Force Microscopy. General Reanimatology. (In Russ.) https://doi.org/10.15360/1813-9779-2026-5-2724

Views: 69

JATS XML


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1813-9779 (Print)
ISSN 2411-7110 (Online)