Mesenchymal stem cells- derived exosomes inhibit the expression of Aquaporin-5 and EGFR in HCT-116 human colorectal carcinoma cell line.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2022-09-16 DOI:10.1186/s12860-022-00439-0
Amir Hossein Mansourabadi, Azin Aghamajidi, Fatemeh Faraji, Shirin Taghizadeh, Leila Mohamed Khosroshahi, Mona Bahramkiya, Maryam Azimi
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引用次数: 2

Abstract

Background: Aquaporins are channel proteins, form pores in the membrane of biological cells to facilitate the transcellular and transepithelial water movement. The role of Aquaporins in carcinogenesis has become an area of interest. In this study, we aimed to investigate the effects of adipose-derived mesenchymal stem cells secreted exosomes on the expression of aquaporin 5 and EGFR genes in the HCT-116 tumor cell line.

Methods and results: Surface antigenic profile of Ad-MSCs was evaluated using specific markers. Exosomes were purified from the Ad-MSc supernatant while the quality and the shape of isolated exosomes were assessed by western blot and transmission electron microscopy (TEM) respectively. HCT-116 cells were co-cultured with MSC-conditioned medium (MSC-CM) and/or with 100 μg/ml of MSC-derived exosomes for 48 h and. Real-time PCR was carried out to determine the expression of aquaporin5 and EGFR in HCT-116. Relative expression levels were calculated using the 2-ΔΔct method. Our result showed that AQP5 and EGFR mRNA levels were significantly reduced in CM and/or exosomes treated HCT116 compare to the control group (P-value < 0.05).

Conclusion: The current study showed that MSC derived exosomes could inhibit expression of two important molecules involved in tumor progression. Hence it seems MSCs-derived exosomes may hold a hopeful future as drug delivery vehicles which need the furtherer investigation.

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间充质干细胞来源的外泌体抑制HCT-116人结直肠癌细胞系水通道蛋白-5和EGFR的表达。
背景:水通道蛋白是一种通道蛋白,在生物细胞的膜上形成孔隙,促进水的跨细胞和跨上皮运动。水通道蛋白在癌变中的作用已成为一个令人感兴趣的领域。在本研究中,我们旨在研究脂肪源性间充质干细胞分泌外泌体对HCT-116肿瘤细胞系水通道蛋白5和EGFR基因表达的影响。方法和结果:采用特异性标记评价Ad-MSCs的表面抗原谱。从Ad-MSc上清液中纯化外泌体,分别用western blot和透射电镜(TEM)评价外泌体的质量和形状。将HCT-116细胞与msc条件培养基(MSC-CM)和/或100 μg/ml的msc来源的外泌体共培养48 h。采用Real-time PCR检测水通道蛋白5和EGFR在HCT-116中的表达。采用2-ΔΔct方法计算相对表达量。我们的研究结果显示,与对照组相比,处理HCT116的CM和/或外泌体中AQP5和EGFR mRNA水平显著降低(p值)。结论:目前的研究表明,MSC衍生的外泌体可以抑制两种参与肿瘤进展的重要分子的表达。因此,mscs衍生的外泌体作为药物递送载体具有广阔的前景,有待进一步研究。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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