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Impact of Double-Stranded RNA Internalization on Hematopoietic Progenitors and Krebs-2 Cells and Mechanism. / Ritter, Genrikh S.; Proskurina, Anastasia S.; Meschaninova, Maria I. и др.

в: International Journal of Molecular Sciences, Том 24, № 5, 4858, 02.03.2023.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Ritter, GS, Proskurina, AS, Meschaninova, MI, Potter, EA, Petrova, DD, Ruzanova, VS, Dolgova, EV, Kirikovich, SS, Levites, EV, Efremov, YR, Nikolin, VP, Popova, NA, Venyaminova, AG, Taranov, OS, Ostanin, AA, Chernykh, ER, Kolchanov, NA & Bogachev, SS 2023, 'Impact of Double-Stranded RNA Internalization on Hematopoietic Progenitors and Krebs-2 Cells and Mechanism', International Journal of Molecular Sciences, Том. 24, № 5, 4858. https://doi.org/10.3390/ijms24054858

APA

Ritter, G. S., Proskurina, A. S., Meschaninova, M. I., Potter, E. A., Petrova, D. D., Ruzanova, V. S., Dolgova, E. V., Kirikovich, S. S., Levites, E. V., Efremov, Y. R., Nikolin, V. P., Popova, N. A., Venyaminova, A. G., Taranov, O. S., Ostanin, A. A., Chernykh, E. R., Kolchanov, N. A., & Bogachev, S. S. (2023). Impact of Double-Stranded RNA Internalization on Hematopoietic Progenitors and Krebs-2 Cells and Mechanism. International Journal of Molecular Sciences, 24(5), [4858]. https://doi.org/10.3390/ijms24054858

Vancouver

Ritter GS, Proskurina AS, Meschaninova MI, Potter EA, Petrova DD, Ruzanova VS и др. Impact of Double-Stranded RNA Internalization on Hematopoietic Progenitors and Krebs-2 Cells and Mechanism. International Journal of Molecular Sciences. 2023 март 2;24(5):4858. doi: 10.3390/ijms24054858

Author

Ritter, Genrikh S. ; Proskurina, Anastasia S. ; Meschaninova, Maria I. и др. / Impact of Double-Stranded RNA Internalization on Hematopoietic Progenitors and Krebs-2 Cells and Mechanism. в: International Journal of Molecular Sciences. 2023 ; Том 24, № 5.

BibTeX

@article{b2c3cb6fcfc54595a306b36b59f49ceb,
title = "Impact of Double-Stranded RNA Internalization on Hematopoietic Progenitors and Krebs-2 Cells and Mechanism",
abstract = "It is well-established that double-stranded RNA (dsRNA) exhibits noticeable radioprotective and radiotherapeutic effects. The experiments conducted in this study directly demonstrated that dsRNA was delivered into the cell in its native form and that it induced hematopoietic progenitor proliferation. The 68 bp synthetic dsRNA labeled with 6-carboxyfluorescein (FAM) was internalized into mouse hematopoietic progenitors, c-Kit+ (a marker of long-term hematopoietic stem cells) cells and CD34+ (a marker of short-term hematopoietic stem cells and multipotent progenitors) cells. Treating bone marrow cells with dsRNA stimulated the growth of colonies, mainly cells of the granulocyte–macrophage lineage. A total of 0.8% of Krebs-2 cells internalized FAM-dsRNA and were simultaneously CD34+ cells. dsRNA in its native state was delivered into the cell, where it was present without any signs of processing. dsRNA binding to a cell was independent of cell charge. dsRNA internalization was related to the receptor-mediated process that requires energy from ATP. Synthetic dsRNA did not degrade in the bloodstream for at least 2 h. Hematopoietic precursors that had captured dsRNA reinfused into the bloodstream and populated the bone marrow and spleen. This study, for the first time, directly proved that synthetic dsRNA is internalized into a eukaryotic cell via a natural mechanism.",
keywords = "Krebs-2 cancer stem cells, dsRNA, hematopoietic progenitors, internalization, stimulation of colony growth, RNA, Double-Stranded/pharmacology, Cells, Cultured, Hematopoietic Stem Cells/metabolism, Animals, Antigens, CD34/metabolism, Bone Marrow/metabolism, Mice, Bone Marrow Cells/metabolism",
author = "Ritter, {Genrikh S.} and Proskurina, {Anastasia S.} and Meschaninova, {Maria I.} and Potter, {Ekaterina A.} and Petrova, {Daria D.} and Ruzanova, {Vera S.} and Dolgova, {Evgeniya V.} and Kirikovich, {Svetlana S.} and Levites, {Evgeniy V.} and Efremov, {Yaroslav R.} and Nikolin, {Valeriy P.} and Popova, {Nelly A.} and Venyaminova, {Aliya G.} and Taranov, {Oleg S.} and Ostanin, {Alexandr A.} and Chernykh, {Elena R.} and Kolchanov, {Nikolay A.} and Bogachev, {Sergey S.}",
note = "This research was funded by the Russian Ministry of Science and High Education via the Institute of Cytology and Genetics [State Budget Project No FWNR-2022-0016]. The authors are grateful for the additional financial help for Inga N. Zaitseva and Aleksey A. Purtov. Публикация для корректировки.",
year = "2023",
month = mar,
day = "2",
doi = "10.3390/ijms24054858",
language = "English",
volume = "24",
journal = "International Journal of Molecular Sciences",
issn = "1661-6596",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "5",

}

RIS

TY - JOUR

T1 - Impact of Double-Stranded RNA Internalization on Hematopoietic Progenitors and Krebs-2 Cells and Mechanism

AU - Ritter, Genrikh S.

AU - Proskurina, Anastasia S.

AU - Meschaninova, Maria I.

AU - Potter, Ekaterina A.

AU - Petrova, Daria D.

AU - Ruzanova, Vera S.

AU - Dolgova, Evgeniya V.

AU - Kirikovich, Svetlana S.

AU - Levites, Evgeniy V.

AU - Efremov, Yaroslav R.

AU - Nikolin, Valeriy P.

AU - Popova, Nelly A.

AU - Venyaminova, Aliya G.

AU - Taranov, Oleg S.

AU - Ostanin, Alexandr A.

AU - Chernykh, Elena R.

AU - Kolchanov, Nikolay A.

AU - Bogachev, Sergey S.

N1 - This research was funded by the Russian Ministry of Science and High Education via the Institute of Cytology and Genetics [State Budget Project No FWNR-2022-0016]. The authors are grateful for the additional financial help for Inga N. Zaitseva and Aleksey A. Purtov. Публикация для корректировки.

PY - 2023/3/2

Y1 - 2023/3/2

N2 - It is well-established that double-stranded RNA (dsRNA) exhibits noticeable radioprotective and radiotherapeutic effects. The experiments conducted in this study directly demonstrated that dsRNA was delivered into the cell in its native form and that it induced hematopoietic progenitor proliferation. The 68 bp synthetic dsRNA labeled with 6-carboxyfluorescein (FAM) was internalized into mouse hematopoietic progenitors, c-Kit+ (a marker of long-term hematopoietic stem cells) cells and CD34+ (a marker of short-term hematopoietic stem cells and multipotent progenitors) cells. Treating bone marrow cells with dsRNA stimulated the growth of colonies, mainly cells of the granulocyte–macrophage lineage. A total of 0.8% of Krebs-2 cells internalized FAM-dsRNA and were simultaneously CD34+ cells. dsRNA in its native state was delivered into the cell, where it was present without any signs of processing. dsRNA binding to a cell was independent of cell charge. dsRNA internalization was related to the receptor-mediated process that requires energy from ATP. Synthetic dsRNA did not degrade in the bloodstream for at least 2 h. Hematopoietic precursors that had captured dsRNA reinfused into the bloodstream and populated the bone marrow and spleen. This study, for the first time, directly proved that synthetic dsRNA is internalized into a eukaryotic cell via a natural mechanism.

AB - It is well-established that double-stranded RNA (dsRNA) exhibits noticeable radioprotective and radiotherapeutic effects. The experiments conducted in this study directly demonstrated that dsRNA was delivered into the cell in its native form and that it induced hematopoietic progenitor proliferation. The 68 bp synthetic dsRNA labeled with 6-carboxyfluorescein (FAM) was internalized into mouse hematopoietic progenitors, c-Kit+ (a marker of long-term hematopoietic stem cells) cells and CD34+ (a marker of short-term hematopoietic stem cells and multipotent progenitors) cells. Treating bone marrow cells with dsRNA stimulated the growth of colonies, mainly cells of the granulocyte–macrophage lineage. A total of 0.8% of Krebs-2 cells internalized FAM-dsRNA and were simultaneously CD34+ cells. dsRNA in its native state was delivered into the cell, where it was present without any signs of processing. dsRNA binding to a cell was independent of cell charge. dsRNA internalization was related to the receptor-mediated process that requires energy from ATP. Synthetic dsRNA did not degrade in the bloodstream for at least 2 h. Hematopoietic precursors that had captured dsRNA reinfused into the bloodstream and populated the bone marrow and spleen. This study, for the first time, directly proved that synthetic dsRNA is internalized into a eukaryotic cell via a natural mechanism.

KW - Krebs-2 cancer stem cells

KW - dsRNA

KW - hematopoietic progenitors

KW - internalization

KW - stimulation of colony growth

KW - RNA, Double-Stranded/pharmacology

KW - Cells, Cultured

KW - Hematopoietic Stem Cells/metabolism

KW - Animals

KW - Antigens, CD34/metabolism

KW - Bone Marrow/metabolism

KW - Mice

KW - Bone Marrow Cells/metabolism

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85149965037&origin=inward&txGid=647096703d01334b0fd1e82737a62515

UR - https://www.mendeley.com/catalogue/a37f4ce3-ccaf-3df2-86df-0e3723eababe/

U2 - 10.3390/ijms24054858

DO - 10.3390/ijms24054858

M3 - Article

C2 - 36902311

VL - 24

JO - International Journal of Molecular Sciences

JF - International Journal of Molecular Sciences

SN - 1661-6596

IS - 5

M1 - 4858

ER -

ID: 59242607