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西罗莫司对K562细胞系及获得性纯红细胞再生障碍原代细胞红系分化作用的研究

OBJECTIVE: To understand the effect of sirolimus on the erythropoiesis of K562 cell line and bone marrow cells from pure red cell aplasia (PRCA) patients and normal controls. METHODS: Different concentrations (10, 100, 1 000 nmol/L) of sirolimus were added to the K562 cell line or bone marrow cells...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342129/
https://www.ncbi.nlm.nih.gov/pubmed/29779328
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2018.04.011
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collection PubMed
description OBJECTIVE: To understand the effect of sirolimus on the erythropoiesis of K562 cell line and bone marrow cells from pure red cell aplasia (PRCA) patients and normal controls. METHODS: Different concentrations (10, 100, 1 000 nmol/L) of sirolimus were added to the K562 cell line or bone marrow cells from PRCA patients or normal controls and cultured 14 days for BFU-E formation. Meanwhile, sirolimus was also added to the serum treated PRCA bone marrow cells to cultivate for the same priod of time. RESULTS: Neither K562 cells, bone marrow cells from PRCA patients or normal controls showed any difference when sirolimus was added to the culture system for BFU-E. However, BFU-E formation decreased after serum was added in PRCA patients (76.40±22.48 vs 136.33±12.58, t=−4.329, P=0.001) and this suppression of BFU-E was partly corrected by 1 000 nmol/L sirolimus treatment (97.14±15.83 vs 76.40±22.48, P=0.038). CONCLUSION: Sirolimus may modulate the suppression of erythropoiesis by serum instead of directly stimulate the growth of red blood cells in PRCA patients.
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spelling pubmed-73421292020-07-16 西罗莫司对K562细胞系及获得性纯红细胞再生障碍原代细胞红系分化作用的研究 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To understand the effect of sirolimus on the erythropoiesis of K562 cell line and bone marrow cells from pure red cell aplasia (PRCA) patients and normal controls. METHODS: Different concentrations (10, 100, 1 000 nmol/L) of sirolimus were added to the K562 cell line or bone marrow cells from PRCA patients or normal controls and cultured 14 days for BFU-E formation. Meanwhile, sirolimus was also added to the serum treated PRCA bone marrow cells to cultivate for the same priod of time. RESULTS: Neither K562 cells, bone marrow cells from PRCA patients or normal controls showed any difference when sirolimus was added to the culture system for BFU-E. However, BFU-E formation decreased after serum was added in PRCA patients (76.40±22.48 vs 136.33±12.58, t=−4.329, P=0.001) and this suppression of BFU-E was partly corrected by 1 000 nmol/L sirolimus treatment (97.14±15.83 vs 76.40±22.48, P=0.038). CONCLUSION: Sirolimus may modulate the suppression of erythropoiesis by serum instead of directly stimulate the growth of red blood cells in PRCA patients. Editorial office of Chinese Journal of Hematology 2018-04 /pmc/articles/PMC7342129/ /pubmed/29779328 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2018.04.011 Text en 2018年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
西罗莫司对K562细胞系及获得性纯红细胞再生障碍原代细胞红系分化作用的研究
title 西罗莫司对K562细胞系及获得性纯红细胞再生障碍原代细胞红系分化作用的研究
title_full 西罗莫司对K562细胞系及获得性纯红细胞再生障碍原代细胞红系分化作用的研究
title_fullStr 西罗莫司对K562细胞系及获得性纯红细胞再生障碍原代细胞红系分化作用的研究
title_full_unstemmed 西罗莫司对K562细胞系及获得性纯红细胞再生障碍原代细胞红系分化作用的研究
title_short 西罗莫司对K562细胞系及获得性纯红细胞再生障碍原代细胞红系分化作用的研究
title_sort 西罗莫司对k562细胞系及获得性纯红细胞再生障碍原代细胞红系分化作用的研究
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342129/
https://www.ncbi.nlm.nih.gov/pubmed/29779328
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2018.04.011
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