Cargando…

骨髓增生异常综合征患者有核红细胞自噬水平的研究

OBJECTIVE: To investigate the change of autophagy level of bone marrow nucleated red blood cell (RBC) in patients with myelodysplastic syndromes (MDS). METHODS: Fifty-four MDS patients and thirty-three controls were enrolled in this study. The mitophagy were observed by transmission electron microsc...

Descripción completa

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354195/
https://www.ncbi.nlm.nih.gov/pubmed/28565745
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.05.015
_version_ 1783558040843190272
collection PubMed
description OBJECTIVE: To investigate the change of autophagy level of bone marrow nucleated red blood cell (RBC) in patients with myelodysplastic syndromes (MDS). METHODS: Fifty-four MDS patients and thirty-three controls were enrolled in this study. The mitophagy were observed by transmission electron microscopy (TEM). The level of autophagy-associated protein LC3B in GlycoA(+) nucleated RBC was measured by flow cytometry. The expressions of ULK1 and mTOR mRNA in GlycoA(+) nucleated RBC were measured by real-time PCR. The expression of the mitochondrial outer membrane protein TOM20 in GlycoA(+) nucleated RBC was detected by Western blot. RESULTS: Autophagosomes or autolysosomes were scarcely observed by TEM in MDS patients. The expression of LC3B in GlycoA(+) nucleated RBC in high-risk MDS patients (0.22±0.12) was significantly lower than that in normal controls (0.43±0.22, P<0.001), and lower than that in low-risk MDS patients (0.40±0.16, P=0.001). The expression of AMPK [0.26 (0.60)] in GlycoA(+) nucleated RBC in high-risk MDS patients was significantly lower than that in controls [1.00 (2.07), P<0.017). The expression of ULK1 mRNA in GlycoA(+) nucleated RBC in high-risk MDS patients [0.27 (3.31)] was significantly lower than that in controls [1.07 (4.41), P<0.017]. The level of mTOR mRNA in GlycoA(+) nucleated RBC in high-risk MDS patients [1.82 (3.74)] was significantly higher than that in controls [1.26 (1.38), P<0.017]. The level of LC3B in GlycoA(+) nucleated RBC was negatively correlated with the HGB (r=0.529, P=0.009) in high-risk MDS patients. The expression of mitochondrial outer membrane protein TOM20 in high-risk MDS patients was 9.42±4.42. CONCLUSION: Autophagy is impaired in nucleated RBC of MDS patients.
format Online
Article
Text
id pubmed-7354195
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Editorial office of Chinese Journal of Hematology
record_format MEDLINE/PubMed
spelling pubmed-73541952020-07-16 骨髓增生异常综合征患者有核红细胞自噬水平的研究 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To investigate the change of autophagy level of bone marrow nucleated red blood cell (RBC) in patients with myelodysplastic syndromes (MDS). METHODS: Fifty-four MDS patients and thirty-three controls were enrolled in this study. The mitophagy were observed by transmission electron microscopy (TEM). The level of autophagy-associated protein LC3B in GlycoA(+) nucleated RBC was measured by flow cytometry. The expressions of ULK1 and mTOR mRNA in GlycoA(+) nucleated RBC were measured by real-time PCR. The expression of the mitochondrial outer membrane protein TOM20 in GlycoA(+) nucleated RBC was detected by Western blot. RESULTS: Autophagosomes or autolysosomes were scarcely observed by TEM in MDS patients. The expression of LC3B in GlycoA(+) nucleated RBC in high-risk MDS patients (0.22±0.12) was significantly lower than that in normal controls (0.43±0.22, P<0.001), and lower than that in low-risk MDS patients (0.40±0.16, P=0.001). The expression of AMPK [0.26 (0.60)] in GlycoA(+) nucleated RBC in high-risk MDS patients was significantly lower than that in controls [1.00 (2.07), P<0.017). The expression of ULK1 mRNA in GlycoA(+) nucleated RBC in high-risk MDS patients [0.27 (3.31)] was significantly lower than that in controls [1.07 (4.41), P<0.017]. The level of mTOR mRNA in GlycoA(+) nucleated RBC in high-risk MDS patients [1.82 (3.74)] was significantly higher than that in controls [1.26 (1.38), P<0.017]. The level of LC3B in GlycoA(+) nucleated RBC was negatively correlated with the HGB (r=0.529, P=0.009) in high-risk MDS patients. The expression of mitochondrial outer membrane protein TOM20 in high-risk MDS patients was 9.42±4.42. CONCLUSION: Autophagy is impaired in nucleated RBC of MDS patients. Editorial office of Chinese Journal of Hematology 2017-05 /pmc/articles/PMC7354195/ /pubmed/28565745 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.05.015 Text en 2017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
骨髓增生异常综合征患者有核红细胞自噬水平的研究
title 骨髓增生异常综合征患者有核红细胞自噬水平的研究
title_full 骨髓增生异常综合征患者有核红细胞自噬水平的研究
title_fullStr 骨髓增生异常综合征患者有核红细胞自噬水平的研究
title_full_unstemmed 骨髓增生异常综合征患者有核红细胞自噬水平的研究
title_short 骨髓增生异常综合征患者有核红细胞自噬水平的研究
title_sort 骨髓增生异常综合征患者有核红细胞自噬水平的研究
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354195/
https://www.ncbi.nlm.nih.gov/pubmed/28565745
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.05.015
work_keys_str_mv AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū
AT gǔsuǐzēngshēngyìchángzōnghézhēnghuànzhěyǒuhéhóngxìbāozìshìshuǐpíngdeyánjiū