来自牙髓和脂肪组织的人间充质干细胞的比较转录组学分析。

IF 1.1 Q4 CELL & TISSUE ENGINEERING
Journal of Stem Cells & Regenerative Medicine Pub Date : 2019-05-30 eCollection Date: 2019-01-01
Atsushi Terunuma, Keisuke Ashiba, Tsubasa Takane, Yosuke Sakaguchi, Hiroshi Terunuma
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引用次数: 0

摘要

目的:从人体多种组织中分离到间充质干细胞。尽管它们具有自我更新和多能性的干细胞基本特征,但它们似乎也具有不同的特征,这取决于它们来自的组织类型。当开发基于干细胞的疗法时,应选择具有最理想特征的间充质干细胞。然而,我们对MSCs的组织类型特异性特征的了解是有限的。我们比较研究了不同组织类型间充质干细胞的基因表达谱,并预测了每种类型间充质干细胞适合的靶疾病。方法:我们从人牙髓和脂肪组织标本中获取MSCs,并对其进行基因表达芯片分析。利用基因注释富集分析鉴定各组织类型间充质干细胞的特征基因表达特征。结果:牙髓来源的MSCs表现出神经元生长的基因表达特征,而脂肪组织来源的MSCs表现出血管生成和毛发生长的基因表达特征。来自每种组织类型的间充质干细胞表达一组离散的基因编码分泌肽,这可能作为旁分泌因子。结论:来自不同组织类型的间充质干细胞表现出不同的基因表达特征,这提示了间充质干细胞和干细胞条件培养基在临床应用中的靶疾病。通过将分析扩展到广泛组织类型的间充质干细胞,并采用多种组学方法,可以生成间充质干细胞和治疗靶点的目录。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparative transcriptomic analysis of human mesenchymal stem cells derived from dental pulp and adipose tissues.

Comparative transcriptomic analysis of human mesenchymal stem cells derived from dental pulp and adipose tissues.

Comparative transcriptomic analysis of human mesenchymal stem cells derived from dental pulp and adipose tissues.

Comparative transcriptomic analysis of human mesenchymal stem cells derived from dental pulp and adipose tissues.

Objective: Mesenchymal stem cells (MSCs) have been isolated from various human tissues. Although they share cardinal stem cell features of self-renewal and multi-potency, they also seem to possess distinct characteristics depending on the tissue types they originated from. When developing stem cell-based therapies, MSCs with the most desirable characteristics should be chosen. However, our knowledge on tissue type-specific characteristics of MSCs is limited. Here, we comparatively studied the gene expression profiles of MSCs from different tissue types, and predicted target diseases suitable for each type of MSCs. Methods: We harvested MSCs from human dental pulp and adipose tissue specimens and subjected them to gene expression microarray analysis. Characteristic gene expression signatures of the MSCs from each tissue type were identified using gene-annotation enrichment analysis. Results: Dental pulp-derived MSCs exhibited gene expression signatures of neuronal growth, while adipose tissue-derived MSCs exhibited signatures of angiogenesis and hair growth. MSCs from each tissue type expressed a discrete set of genes encoding secretory peptides, which may function as paracrine factors. Conclusions: MSCs derived from different tissue types demonstrated distinct gene expression signatures, which are suggestive of target diseases in clinical applications of the MSCs and stem cell-conditioned media. By expanding the analysis to MSCs from a wide range of tissue types, and by employing multiple omics approaches, a catalogue of MSCs and therapeutic targets can be generated.

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来源期刊
CiteScore
3.40
自引率
0.00%
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审稿时长
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