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新生儿性别对脐血CD34细胞扩增及基因表达的影响。

Influence of neonatal gender on cord blood CD34 cell amplification and gene expression.

作者信息

Zhou Liping, Che Zhe, Zhang Xiaowei, Zhou Panpan, Li Xue, Xu Xuejing, Shi Qing, Li Dong, Ju Xiuli

机构信息

Department of Pediatrics, The Sixth People's Hospital of Ji'nan, Jinan, Shandong 250200, P.R. China.

Cryomedicine Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong 250012, P.R. China.

出版信息

Exp Ther Med. 2019 Jul;18(1):105-118. doi: 10.3892/etm.2019.7549. Epub 2019 May 7.

Abstract

The present study attempted to evaluate whether neonatal gender affects the hematopoietic potential of cord blood (CB) transplants and, if so, to determine the underlying molecular mechanisms. CD34 cells from CB were isolated and divided into male and female groups. CD34CD38 cell populations were then compared using fluorescence-assisted cell sorting (FACS) and a colony formation assay was performed. Next, a Genechip microarray analysis was used to identify differentially expressed genes (DEGs). Finally, the Genechip results were validated by FACS analysis. It was revealed that the male group had higher amplification efficiency. Gene ontology analysis indicated differences in the biological function of the DEGs between the two groups. Kyoto Encyclopedia of Genes and Genomes analysis suggested that the hematopoietic cell lineage signaling pathway was upregulated in the male group along with high expression levels of genes including interleukin (IL) 6 signal transducer (glycoprotein 130), IL-7 and IL-7 receptor. It was speculated that this may be partially due to numerous upregulated DEGs being involved in chromosomal segregation and hematopoietic cell lineage signaling pathways in CD34 cells from the male group.

摘要

本研究试图评估新生儿性别是否会影响脐血(CB)移植的造血潜能,如果是,则确定其潜在的分子机制。从CB中分离出CD34细胞,并分为雄性和雌性组。然后使用荧光辅助细胞分选(FACS)比较CD34CD38细胞群体,并进行集落形成试验。接下来,使用基因芯片微阵列分析来鉴定差异表达基因(DEG)。最后,通过FACS分析验证基因芯片结果。结果显示,雄性组具有更高的扩增效率。基因本体分析表明两组之间DEG的生物学功能存在差异。京都基因与基因组百科全书分析表明,雄性组中造血细胞谱系信号通路上调,同时包括白细胞介素(IL)6信号转导子(糖蛋白130)、IL-7和IL-7受体在内的基因表达水平较高。据推测,这可能部分是由于雄性组CD34细胞中大量上调的DEG参与了染色体分离和造血细胞谱系信号通路。

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