KRAS-dependent sorting of miRNA to exosomes

Author:

Cha Diana J12,Franklin Jeffrey L345,Dou Yongchao6,Liu Qi6,Higginbotham James N34,Demory Beckler Michelle4,Weaver Alissa M378,Vickers Kasey9,Prasad Nirpesh10,Levy Shawn10,Zhang Bing6,Coffey Robert J345,Patton James G12

Affiliation:

1. Department of Biological Sciences, Vanderbilt University Medical Center, Nashville, United States

2. Vanderbilt University, Nashville, United States

3. Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, United States

4. Department of Medicine, Vanderbilt University Medical Center, Nashville, United States

5. Affairs Medical Center, Nashville, United States

6. Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, United States

7. Department of Cancer Biology, Vanderbilt University Medical Center, Nashville, United States

8. Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, United States

9. Department of Cardiology, Vanderbilt University Medical Center, Nashville, United States

10. HudsonAlpha Institute for Biotechnology, Huntsville, United States

Abstract

Mutant KRAS colorectal cancer (CRC) cells release protein-laden exosomes that can alter the tumor microenvironment. To test whether exosomal RNAs also contribute to changes in gene expression in recipient cells, and whether mutant KRAS might regulate the composition of secreted microRNAs (miRNAs), we compared small RNAs of cells and matched exosomes from isogenic CRC cell lines differing only in KRAS status. We show that exosomal profiles are distinct from cellular profiles, and mutant exosomes cluster separately from wild-type KRAS exosomes. miR-10b was selectively increased in wild-type exosomes, while miR-100 was increased in mutant exosomes. Neutral sphingomyelinase inhibition caused accumulation of miR-100 only in mutant cells, suggesting KRAS-dependent miRNA export. In Transwell co-culture experiments, mutant donor cells conferred miR-100-mediated target repression in wild-type-recipient cells. These findings suggest that extracellular miRNAs can function in target cells and uncover a potential new mode of action for mutant KRAS in CRC.

Funder

National Institutes of Health

National Cancer Institute

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3