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心肌细胞微囊泡含有 DNA/RNA 并将生物信息传递给靶细胞。

Cardiomyocyte microvesicles contain DNA/RNA and convey biological messages to target cells.

机构信息

Department of Public Health and Clinical Medicine/Medicine, Umeå University, Umeå, Sweden.

出版信息

PLoS One. 2012;7(4):e34653. doi: 10.1371/journal.pone.0034653. Epub 2012 Apr 10.

Abstract

BACKGROUND

Shedding microvesicles are membrane released vesicles derived directly from the plasma membrane. Exosomes are released membrane vesicles of late endosomal origin that share structural and biochemical characteristics with prostasomes. Microvesicles/exosomes can mediate messages between cells and affect various cell-related processes in their target cells. We describe newly detected microvesicles/exosomes from cardiomyocytes and depict some of their biological functions.

METHODOLOGY/PRINCIPAL FINDINGS: Microvesicles/exosomes from media of cultured cardiomyocytes derived from adult mouse heart were isolated by differential centrifugation including preparative ultracentrifugation and identified by transmission electron microscopy and flow cytometry. They were surrounded by a bilayered membrane and flow cytometry revealed presence of both caveolin-3 and flotillin-1 while clathrin and annexin-2 were not detected. Microvesicle/exosome mRNA was identified and out of 1520 detected mRNA, 423 could be directly connected in a biological network. Furthermore, by a specific technique involving TDT polymerase, 343 different chromosomal DNA sequences were identified in the microvesicles/exosomes. Microvesicle/exosomal DNA transfer was possible into target fibroblasts, where exosomes stained for DNA were seen in the fibroblast cytosol and even in the nuclei. The gene expression was affected in fibroblasts transfected by microvesicles/exosomes and among 333 gene expression changes there were 175 upregulations and 158 downregulations compared with controls.

CONCLUSIONS/SIGNIFICANCE: Our study suggests that microvesicles/exosomes released from cardiomyocytes, where we propose that exosomes derived from cardiomyocytes could be denoted "cardiosomes", can be involved in a metabolic course of events in target cells by facilitating an array of metabolism-related processes including gene expression changes.

摘要

背景

脱落的微泡是直接来源于质膜的膜释放小泡。外体是晚期内体起源的释放膜小泡,与前列腺小体具有结构和生化特征。微泡/外体可以在细胞之间传递信息,并影响靶细胞中的各种与细胞相关的过程。我们描述了来自心肌细胞的新检测到的微泡/外体,并描述了它们的一些生物学功能。

方法/主要发现:通过包括差速离心(包括制备超速离心)在内的差异离心,从成年小鼠心脏来源的培养心肌细胞的培养基中分离出微泡/外体,并通过透射电子显微镜和流式细胞术进行鉴定。它们被双层膜包围,流式细胞术显示存在窖蛋白-3 和 flotillin-1,而未检测到网格蛋白和膜联蛋白-2。微泡/外体 mRNA 被鉴定,在检测到的 1520 个 mRNA 中,有 423 个可以直接连接在一个生物网络中。此外,通过一种涉及 TDT 聚合酶的特殊技术,在微泡/外体中鉴定出 343 个不同的染色体 DNA 序列。微泡/外体 DNA 转移是可能的,进入靶成纤维细胞,在成纤维细胞胞质溶胶中甚至在细胞核中都可以看到外体染色的 DNA。转染微泡/外体的成纤维细胞中的基因表达受到影响,与对照组相比,333 个基因表达变化中有 175 个上调和 158 个下调。

结论/意义:我们的研究表明,心肌细胞释放的微泡/外体,我们提出来自心肌细胞的外体可以被称为“心肌小体”,可以通过促进一系列与代谢相关的过程,包括基因表达变化,参与靶细胞中的代谢事件过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f465/3323564/1f0e6d372d46/pone.0034653.g001.jpg

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