细小病毒B19感染可能通过改变人骨髓间充质干细胞分化而潜在地决定造血的命运

IF 0.4 Q4 PEDIATRICS
Azin Elmi, Amir Atashi, Nematollah Gheibi, Shahin Amiri, Monireh Ajami, Mansoureh Ajami, Razieh Mohammadihaji, Naeimeh Khodabandeloo, Mehdi Azad
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引用次数: 0

摘要

背景:人骨髓间充质干细胞(hBM-MSCs)作为造血的支持细胞,可分化为成骨细胞和脂肪细胞。研究表明,细小病毒B19 (Parvovirus B19, B19V)感染hBM-MSCs可影响hBM-MSCs的分化能力。本研究旨在评估B19V对hBM-MSCs分化的影响。材料与方法:本实验采用hBM-MSCs培养至传代3。随后采用核转染将含有B19V基因组的质粒送入细胞。转染后的细胞分化为成骨细胞和脂肪细胞。转染后第14天进行qRT-PCR分析分化情况。 结果:诱导后第14天,与对照组相比,脂肪细胞特异性基因(PPARγ和LPL)表达显著增加(p>0.05),骨细胞特异性基因(RUNX2和骨钙素)表达略有下降(p>0.05)。结论:B19V感染可促进hBM-MSCs向脂肪细胞分化,影响骨髓微环境及造血功能
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Parvovirus B19 Infection May Potentially Determine the Fate of Hematopoiesis by Altering the Human Bone Marrow Mesenchymal Stem Cells Differentiation
Background: Human bone marrow mesenchymal stem cells (hBM-MSCs), as supporters for hematopoiesis, differentiate into osteoblasts and adipocytes. Studies showed that infection of hBM-MSCs by Parvovirus B19 (B19V) can affect the differentiation capability of hBM-MSCs. This study aims to evaluate B19V effects on the differentiation of hBM-MSCs. Materials and Methods: In this experimental study hBM-MSCs were cultured up to passage 3. Nucleofection was subsequently employed to deliver a plasmid containing the B19V genome into the cells. The transfected cells were then differentiated into osteoblast and adipocyte lineages. qRT-PCR was then performed to analyze the differentiation 14 days after transfection. Results: On the 14th day after induction the findings demonstrated a significant increase in adipocyte-specific (PPARγ and LPL) gene expression compared to the control group (p<0.05) and a slight but not statistically significant decrease in the expression of the osteocyte-specific genes (RUNX2 and osteocalcin) (p>0.05). Conclusion: The results suggest that B19V infection can promote the differentiation of hBM-MSCs towards adipocytes and affect the bone marrow microenvironment as well as hematopoiesis
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来源期刊
CiteScore
0.80
自引率
33.30%
发文量
33
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