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[Expression Levels of MiR-451 in Erythroid Differentiation and Its Correlation with Hematological Diseases].
Ling, Ling; Wang, Fang-Fang; Zhou, Shu-Ting; Yang, Lei; Yang, Fan; Yang, Lan; Yu, Duo-Nan.
Afiliación
  • Ling L; Yangzhou University School of Medicine/Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou 225009, Jiangsu Province, China.
  • Wang FF; Clinical Medical College, Yangzhou University/Northern Jiangsu People's Hospital, Yangzhou 225001, Jiangsu Province, China.
  • Zhou ST; Yangzhou University School of Medicine/Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou 225009, Jiangsu Province, China.
  • Yang L; Yangzhou University School of Medicine/Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou 225009, Jiangsu Province, China.
  • Yang F; Yangzhou University School of Medicine/Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou 225009, Jiangsu Province, China.
  • Yang L; Yangzhou University School of Medicine/Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou 225009, Jiangsu Province, China.
  • Yu DN; Yangzhou University School of Medicine/Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou 225009, Jiangsu Province, China,E-mail: dnyu@yzu.edu.cn.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 30(6): 1810-1816, 2022 Dec.
Article en Zh | MEDLINE | ID: mdl-36476908
ABSTRACT

OBJECTIVE:

To investigate the expression of miR-451 during erythroid differentiation and its correlation with hematological diseases.

METHODS:

The expression of miR-451 in erythroid differentiation of mouse hematopoietic stem cells (derived from fetal liver) was analyzed by cell culture, flow cytometry, magnetic bead sorting and qRT-PCR. The expression of miR-451 during erythroid differentiation of mouse erythroid leukemia cells (MEL) was analyzed by cell culture and qRT-PCR. The expression of miR-451 in peripheral blood of mice was detected by qRT-PCR, and the expression of miR-451 in fetal liver (14.5 days) was analyzed by microarray. The nucleated erythroid cells from bone marrow of wild type (WT) mice and ß-thalassemia (ß-thal) mice were sorted by flow cytometry, and the levels of miR-451 and erythroid genes were detected by qRT-PCR. The expression of miR-451 in peripheral blood of patients with clinical hematological diseases was detected by qRT-PCR.

RESULTS:

During the differentiation of mouse hematopoietic stem cells (derived from fetal liver) and MEL cells, the expression levels of miR-451 increased gradually. Compared with WT mice, the expression levels of miR-451 in peripheral blood, 14.5-day fetal liver cells and nucleated erythroid cells (sorted from bone marrow) of ß-thal mice were significantly increased(P<0.05). Many erythroid differentiation genes in nucleated erythroid cells (sorted from bone marrow) of ß-thal mice decreased. Compared with healthy controls, the expression levels of miR-451 was increased in peripheral blood of patients with ß-thalassemia and iron deficiency anemia, while the expression levels of miR-451 was decreased in patients with aplastic anemia and myelodysplastic syndrome.

CONCLUSION:

During erythroid differentiation, the expression levels of miR-451 increases gradually. In hematological diseases, the expression levels of miR-451 is different from that of normal controls, which is expected to become an auxiliary diagnostic index for clinical hematological diseases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Talasemia beta / MicroARNs Límite: Animals Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Asunto de la revista: HEMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Talasemia beta / MicroARNs Límite: Animals Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Asunto de la revista: HEMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: China