DNA-Containing Extracellular Structures of Tumor Cells Inhibit the Formation of Neutrophil Extracellular Traps in vitro

Aim. To study the parameters of formed DNA-containing extracellular structures during co-cultivation of neutrophils from healthy donors, HСT116 adenocarcinoma cells and K562 myeloblastoma. Materials and methods. Erythrocyte sedimentation in EDTA-treated blood was carried out using Dextran 500. The neutrophil-enriched layer of blood plasma was collected. The admixture of mononuclear cells was less than 1%. Platelets were removed using differential centrifugation. Isolated neutrophils in RPMI-1640 medium were used in short-term culture experiments. HCT116 adenocarcinoma and K562 myeloblastoma cells were obtained from the American Type Culture Collection. In the experiments, donor neutrophils and tumor cells were co-cultivated for 3 hours. SYBR Green fluorescence microscopy was used to visualize the DNA-containing extracellular structures formation by cells cultured in RPMI-1640 medium. Results. Neutrophils recognize tumor cells and respond to contact interactions, forming neutrophil extracellular traps in the form of neutrophil networks. Contacts with HCT116 adenocarcinoma cells cause rapid formation of neutrophil web-like structures – within 1 hour. The opening of neutrophil web-like structures induced by contacts with K562 myeloblastoma cells requires a longer incubation (2 hours). HCT116 cells form large bundles of DNAcontaining fibers, which completely inhibit the formation of neutrophil networks. K562 cells suppress neutrophil defense responses by reducing the number and size of neutrophil networks. The effect of inhibition of neutrophil networks by K562 cells is probably due to the action of a soluble factor that suppresses neutrophil functions described earlier. Conclusion. The study shows that both tumor cell lines are capable of suppressing innate immune cell responses through different mechanisms. Adenocarcinoma cells inhibit neutrophil network formation upon direct contact due to the large size DNA-containing fibers they produce. Myeloblastoma cells produce the same effect, probably acting by secreting humoral factors.

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Journal
Bulletin of Siberian Medicine
Published
2025-07-14
DOI
https://doi.org/10.20538/1682-0363-2025-2-36-43
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
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article
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article

DNA-Containing Extracellular Structures of Tumor Cells Inhibit the Formation of Neutrophil Extracellular Traps in vitro

A. E. Kim, M. I. Panina, G. V. Poryadin, J. M. Salmasi et al.
Bulletin of Siberian Medicine
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
article

DNA-Containing Extracellular Structures of Tumor Cells Inhibit the Formation of Neutrophil Extracellular Traps in vitro

A. E. Kim, M. I. Panina, G. V. Poryadin, J. M. Salmasi, А. Н. Казимирский, O. O. Turishcheva, A. G. Chakhalian
article en

Abstract

Aim. To study the parameters of formed DNA-containing extracellular structures during co-cultivation of neutrophils from healthy donors, HСT116 adenocarcinoma cells and K562 myeloblastoma. Materials and methods. Erythrocyte sedimentation in EDTA-treated blood was carried out using Dextran 500. The neutrophil-enriched layer of blood plasma was collected. The admixture of mononuclear cells was less than 1%. Platelets were removed using differential centrifugation. Isolated neutrophils in RPMI-1640 medium were used in short-term culture experiments. HCT116 adenocarcinoma and K562 myeloblastoma cells were obtained from the American Type Culture Collection. In the experiments, donor neutrophils and tumor cells were co-cultivated for 3 hours. SYBR Green fluorescence microscopy was used to visualize the DNA-containing extracellular structures formation by cells cultured in RPMI-1640 medium. Results. Neutrophils recognize tumor cells and respond to contact interactions, forming neutrophil extracellular traps in the form of neutrophil networks. Contacts with HCT116 adenocarcinoma cells cause rapid formation of neutrophil web-like structures – within 1 hour. The opening of neutrophil web-like structures induced by contacts with K562 myeloblastoma cells requires a longer incubation (2 hours). HCT116 cells form large bundles of DNAcontaining fibers, which completely inhibit the formation of neutrophil networks. K562 cells suppress neutrophil defense responses by reducing the number and size of neutrophil networks. The effect of inhibition of neutrophil networks by K562 cells is probably due to the action of a soluble factor that suppresses neutrophil functions described earlier. Conclusion. The study shows that both tumor cell lines are capable of suppressing innate immune cell responses through different mechanisms. Adenocarcinoma cells inhibit neutrophil network formation upon direct contact due to the large size DNA-containing fibers they produce. Myeloblastoma cells produce the same effect, probably acting by secreting humoral factors.

Bulletin of Siberian MedicineVol. 24(2)
Pirogov Russian National Research Medical University (RU)
Openalex Percentile: Top 78%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
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