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包含水凝胶微球的免疫抑制间充质干细胞聚集体促进癌细胞的体外侵袭。

Immunosuppressive mesenchymal stem cells aggregates incorporating hydrogel microspheres promote an in vitro invasion of cancer cells.

作者信息

Nii Teruki, Tabata Yasuhiko

机构信息

Laboratory of Biomaterials, Institute for Frontier Life and Medical Sciences, Kyoto University, 53 Kawara-cho Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.

出版信息

Regen Ther. 2021 Dec 10;18:516-522. doi: 10.1016/j.reth.2021.11.006. eCollection 2021 Dec.

Abstract

INTRODUCTION

The objective of this study is to design a co-culture system of cancer cells and three-dimensional (3D) mesenchymal stem cells (MSC) aggregates for the in vitro evaluation of cancer invasion.

METHODS

First, the MSC of an immunosuppressive phenotype (MSC2) were prepared by the MSC stimulation of polyriboinosinic polyribocytidylic acid. By simple mixing MSC2 and gelatin hydrogel microspheres (GM) in a U-bottomed well of 96 well plates which had been pre-coated with poly (vinyl alcohol), 3D MSC2 aggregates incorporating GM were obtained. The amount of chemokine (C-C motif) ligand 5 (CCL5) secreted from the MSC2 aggregates incorporating GM. Finally, an invasion assay was performed to evaluate the cancer invasion rate by co-cultured cancer cells and the 3D MSC2 incorporating GM.

RESULTS

The amount of CCL5 secreted for the 3D MSC2 aggregates incorporating GM was significantly higher than that of two-dimensional (2D) MSC, 2D MSC2, and 3D MSC aggregates incorporating GM. When MDA-MB-231 human breast cancer cells were co-cultured with the 3D MSC2 aggregates incorporating GM, the invasion rate of cancer cells was significantly high compared with that of 2D MSC or 2D MSC2 and 3D MSC aggregates incorporating GM. In addition, high secretion of matrix metalloproteinase-2 was observed for the 3D MSC2 aggregates/cancer cells system.

CONCLUSIONS

It is concluded that the co-culture system of 3D MSC2 aggregates incorporating GM and cancer cells is promising to evaluate the invasion of cancer cells in vitro.

摘要

引言

本研究的目的是设计一种癌细胞与三维(3D)间充质干细胞(MSC)聚集体的共培养系统,用于体外评估癌症侵袭。

方法

首先,通过用聚肌苷酸-聚胞苷酸刺激MSC制备具有免疫抑制表型的MSC(MSC2)。通过将MSC2与明胶水凝胶微球(GM)简单混合在预先涂有聚乙烯醇的96孔板的U型孔中,获得包含GM的3D MSC2聚集体。检测包含GM的MSC2聚集体分泌的趋化因子(C-C基序)配体5(CCL5)的量。最后,进行侵袭试验以评估共培养的癌细胞与包含GM的3D MSC2的癌症侵袭率。

结果

包含GM的3D MSC2聚集体分泌的CCL5量显著高于二维(2D)MSC、2D MSC2以及包含GM的3D MSC聚集体。当MDA-MB-231人乳腺癌细胞与包含GM的3D MSC2聚集体共培养时,与2D MSC或2D MSC2以及包含GM的3D MSC聚集体相比,癌细胞的侵袭率显著更高。此外,在3D MSC2聚集体/癌细胞系统中观察到基质金属蛋白酶-2的高分泌。

结论

得出结论,包含GM的3D MSC2聚集体与癌细胞的共培养系统有望用于体外评估癌细胞的侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0007/8668441/a371f6d28e29/gr1.jpg

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