Abstract

Exosomes are nanoscale membrane vesicles secreted from many types of cells. Carrying functional molecules, exosomes transfer information between cells and mediate many physiological and pathological processes. In this report, utilizing selective inhibitors, molecular tools, and specific endocytosis markers, the cellular uptake of PC12 cell-derived exosomes was imaged by high-throughput microscopy and statistically analyzed. It was found that the uptake was through clathrin-mediated endocytosis and macropinocytosis. Furthermore, PC12 cell-derived exosomes can enter and deliver microRNAs (miRNAs) into bone marrow-derived mesenchymal stromal cells (BMSCs), and decrease the expression level of transforming growth factor β receptor II (TGFβRII) and tropomyosin-1 (TPM1) through miR-21. These results show the pathway of exosome internalization and demonstrate that tumor cell-derived exosomes regulate target gene expression in normal cells.

Keywords

EndocytosisMicrovesiclesPinocytosisInternalizationCell biologyExosomeClathrinBiologyCaveolaeReceptor-mediated endocytosisMesenchymal stem cellCellChemistrymicroRNASignal transductionBiochemistry

Affiliated Institutions

Related Publications

Publication Info

Year
2014
Type
article
Volume
289
Issue
32
Pages
22258-22267
Citations
676
Access
Closed

External Links

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

676
OpenAlex

Cite This

Tian Tian, Yan-Liang Zhu, Yue-Yuan Zhou et al. (2014). Exosome Uptake through Clathrin-mediated Endocytosis and Macropinocytosis and Mediating miR-21 Delivery. Journal of Biological Chemistry , 289 (32) , 22258-22267. https://doi.org/10.1074/jbc.m114.588046

Identifiers

DOI
10.1074/jbc.m114.588046