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基质金属蛋白酶3基因敲除会削弱实体瘤类器官和癌症细胞外囊泡。

Knockout of MMP3 Weakens Solid Tumor Organoids and Cancer Extracellular Vesicles.

作者信息

Taha Eman A, Sogawa Chiharu, Okusha Yuka, Kawai Hotaka, Oo May Wathone, Elseoudi Abdellatif, Lu Yanyin, Nagatsuka Hitoshi, Kubota Satoshi, Satoh Ayano, Okamoto Kuniaki, Eguchi Takanori

机构信息

Department of Dental Pharmacology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8525, Japan.

Department of Medical Bioengineering, Okayama University Graduate School of Natural Science and Technology, Okayama 700-8530, Japan.

出版信息

Cancers (Basel). 2020 May 16;12(5):1260. doi: 10.3390/cancers12051260.

Abstract

The tumor organoid (tumoroid) model in three-dimensional (3D) culture systems has been developed to reflect more closely the in vivo tumors than 2D-cultured tumor cells. Notably, extracellular vesicles (EVs) are efficiently collectible from the culture supernatant of gel-free tumoroids. Matrix metalloproteinase (MMP) 3 is a multi-functional factor playing crucial roles in tumor progression. However, roles of MMP3 within tumor growth and EVs have not unveiled. Here, we investigated the protumorigenic roles of MMP3 on integrities of tumoroids and EVs. We generated MMP3-knockout (KO) cells using the CRISPR/Cas9 system from rapidly metastatic LuM1 tumor cells. Moreover, we established fluorescent cell lines with palmitoylation signal-fused fluorescent proteins (tdTomato and enhanced GFP). Then we confirmed the exchange of EVs between cellular populations and tumoroids. LuM1-tumoroids released large EVs (200-1000 nm) and small EVs (50-200 nm) while the knockout of MMP3 resulted in the additional release of broken EVs from tumoroids. The loss of MMP3 led to a significant reduction in tumoroid size and the development of the necrotic area within tumoroids. MMP3 and CD9 (a category-1 EV marker tetraspanin protein) were significantly down-regulated in MMP3-KO cells and their EV fraction. Moreover, CD63, another member of the tetraspanin family, was significantly reduced only in the EVs fractions of the MMP3-KO cells compared to their counterpart. These weakened phenotypes of MMP3-KO were markedly rescued by the addition of MMP3-rich EVs or conditioned medium (CM) collected from LuM1-tumoroids, which caused a dramatic rise in the expression of MMP3, CD9, and Ki-67 (a marker of proliferating cells) in the MMP3-null/CD9-low tumoroids. Notably, MMP3 enriched in tumoroids-derived EVs and CM deeply penetrated recipient MMP3-KO tumoroids, resulting in a remarkable enlargement of solid tumoroids, while MMP3-null EVs did not. These data demonstrate that EVs can mediate molecular transfer of MMP3, resulting in increasing the proliferation and tumorigenesis, indicating crucial roles of MMP3 in tumor progression.

摘要

三维(3D)培养系统中的肿瘤类器官(肿瘤样物)模型已被开发出来,以比二维培养的肿瘤细胞更紧密地反映体内肿瘤情况。值得注意的是,细胞外囊泡(EVs)可从无凝胶肿瘤样物的培养上清液中有效收集。基质金属蛋白酶(MMP)3是一种多功能因子,在肿瘤进展中起关键作用。然而,MMP3在肿瘤生长和细胞外囊泡中的作用尚未明确。在此,我们研究了MMP3对肿瘤样物和细胞外囊泡完整性的促肿瘤作用。我们使用CRISPR/Cas9系统从快速转移的LuM1肿瘤细胞中生成了MMP3基因敲除(KO)细胞。此外,我们建立了带有棕榈酰化信号融合荧光蛋白(tdTomato和增强型绿色荧光蛋白)的荧光细胞系。然后我们证实了细胞群体与肿瘤样物之间细胞外囊泡的交换。LuM1肿瘤样物释放大细胞外囊泡(200 - 1000纳米)和小细胞外囊泡(50 - 200纳米),而MMP3的敲除导致肿瘤样物额外释放破碎的细胞外囊泡。MMP3的缺失导致肿瘤样物大小显著减小以及肿瘤样物内坏死区域的出现。MMP3和CD9(一种1类细胞外囊泡标志物四跨膜蛋白)在MMP3 - KO细胞及其细胞外囊泡部分中显著下调。此外,与对照相比,四跨膜蛋白家族的另一个成员CD63仅在MMP3 - KO细胞的细胞外囊泡部分中显著减少。通过添加富含MMP3的细胞外囊泡或从LuM1肿瘤样物收集的条件培养基(CM),MMP3 - KO的这些减弱表型得到显著挽救,这导致MMP3基因缺失/CD9低表达的肿瘤样物中MMP3、CD9和Ki - 67(增殖细胞标志物)的表达急剧上升。值得注意的是,肿瘤样物来源的细胞外囊泡和条件培养基中富集的MMP3深入穿透受体MMP3 - KO肿瘤样物,导致实体肿瘤样物显著增大,而MMP3缺失的细胞外囊泡则不然。这些数据表明细胞外囊泡可以介导MMP3的分子转移,从而导致增殖和肿瘤发生增加,表明MMP3在肿瘤进展中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb19/7281240/0c8752afdbf5/cancers-12-01260-g001.jpg

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