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Cytoskeletal proteins and stem cell markers gene expression in human bone marrow mesenchymal stromal cells after different periods of simulated microgravity

机译:模拟微重力作用不同时间后人骨髓间充质基质细胞中细胞骨架蛋白和干细胞标志物基因的表达

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Mesenchymal stem (stromal) cells (MSCs) are present in a variety of tissues during prenatal and postnatal human development. In adult organism, they are prevalent in bone marrow and supposed to be involved in space-flight induced osteopenia. We studied expression of various genes in human bone marrow MSCs after different terms of simulated microgravity (SMG) provided by Random Positioning Machine. Simulated microgravity induced transient changes in expression level of genes associated with actin cytoskeleton, especially after 48 h of SMG. However, after 120 h exposure in SMG partial restoration of gene expression levels (relative to the control) was found. Similar results were obtained with bmMSCs subjected to 24 h readaptation in static state after 24 h in SMG. Analysis of 84 genes related to identification, growth and differentiation of stem cells revealed that expression of nine genes was changed slightly after 48 h in SMG. More pronounced changes in gene expression of "stem cells markers" were observed after 120 h of simulated microgravity. Among 84 investigated genes, 30 were up-regulated and 24 were down-regulated. Finally, MSCs osteogenesis induced by long-term (10-20 days) simulation of microgravity was accompanied by down-regulation of gene expression of the main osteogenic differentiation markers (ALPL, OMD) and master transcription osteogenic factor of MSCs (Runx2). Thus, our study demonstrated that changes in expression level of some genes associated with actin cytoskeleton and stem cell markers are supposed to be one of the mechanisms, which contribute to precursor's cellular adaptation to the microgravity conditions. These results can clarify genomic mechanisms through which SMG reduces osteogenic differentiation of bmMSCs.
机译:间充质干(基质)细胞(MSCs)存在于人类出生前和出生后的各种组织中。在成年生物中,它们普遍存在于骨髓中,并被认为与航天诱导的骨质减少有关。我们研究了随机定位机提供的不同的模拟微重力(SMG)术语后,人类骨髓MSC中各种基因的表达。模拟微重力诱导与肌动蛋白细胞骨架相关的基因表达水平的瞬时变化,尤其是在SMG 48 h后。然而,在SMG中暴露120小时后,发现基因表达水平的部分恢复(相对于对照)。在SMG中放置24小时后,在静态下对bmMSC进行24小时重新适应后,可获得类似的结果。对与干细胞的鉴定,生长和分化有关的84个基因的分析显示,在SMG中48小时后,9个基因的表达略有改变。在120 h模拟微重力作用下,观察到“干细胞标记”基因表达的更明显变化。在研究的84个基因中,有30个上调而有24个下调。最后,通过长期(10-20天)的微重力模拟诱导的MSC成骨,同时伴随着主要成骨分化标记(ALPL,OMD)和主转录成骨因子(Runx2)基因表达的下调。因此,我们的研究表明,与肌动蛋白细胞骨架和干细胞标志物相关的某些基因表达水平的变化被认为是机制之一,其有助于前体细胞适应微重力条件。这些结果可以阐明SMG减少bmMSC的成骨分化的基因组机制。

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