Hematopoietic stem cell-derived exosomes promote hematopoietic differentiation of mouse embryonic stem cells in vitro via inhibiting the miR126/Notch1 pathway

• Published in: Acta pharmacologica Sinica Vol. 39; no. 4; pp. 552 - 560
• Main Authors: Liao, Feng-Ling, Tan, Lin, Liu, Hua, Wang, Jin-Ju, Ma, Xiao-Tang, Zhao, Bin, Chen, Yanfang, Bihl, Ji, Yang, Yi, Chen, Ri-Ling
• Format: Journal Article
• Language: English
• Published: United States Nature Publishing Group 01.04.2018
• Subjects: Animals; Ataxin; CD34 antigen; Cell culture; Cell differentiation; Cell Differentiation - drug effects; Cell fate; Cell Self Renewal; Embryo cells; Embryos; Exosomes; Exosomes - metabolism; Flow cytometry; Hematopoiesis; Hematopoietic stem cells; Hematopoietic Stem Cells - metabolism; Jagged-1 Protein - metabolism; Jagged1 protein; Mice; MicroRNAs - antagonists & inhibitors; MicroRNAs - metabolism; miRNA; Mouse Embryonic Stem Cells - drug effects; Mouse Embryonic Stem Cells - metabolism; Nanoparticles; Notch1 protein; Receptor, Notch1 - antagonists & inhibitors; Receptor, Notch1 - metabolism; Signal Transduction - drug effects; Stem cell transplantation; Stem cells; Transfection; Ultracentrifugation
• ISSN: 1671-4083; 1745-7254
• DOI: 10.1038/aps.2017.130

Cell-derived exosomes (EXs) can modulate target cell differentiation via microRNAs (miRs) that they carried. Previous studies have shown that miR126 is highly expressed in hematopoietic stem cells (HSCs) and plays a role in hematopoiesis via modulating the Notch pathway that participates in progenitors' cell fate decisions. In this study we investigated whether HSC-derived EXs (HSC-EXs) could affect the differentiation of mouse embryonic stem cells (ESCs) into HSCs. We prepared HSC-EXs , HSC-EXs and HSC-EXs from control HSCs and the HSCs transfected with scramble control or miR126 mimics, respectively. HSC-EXs were isolated by ultracentrifugation and analyzed using nanoparticle tracking analysis. We incubated the collected EXs with mouse ESCs over a 10-d differentiation induction period, during which HSC-EXs and a Notch pathway activator (Jagged1, 100 ng/mL) were added to the cultures every 3 d. After the 10-d differentiation period, the expression levels of miR126, SSEA1, CD117, Sca1, Notch1 and Hes1 in ESCs were assessed. The generated HSCs were validated by flow cytometry using antibodies against HSC markers (CD117, CD34 and Sca1). Our results revealed that: (1) transfection with miR126 mimics significantly increased miR126 levels in HSC-EXs . (2) HSC-EX co-culture promoted mouse ESCs differentiation into HSCs with the most prominent effect found in the HSC-EXs co-culture. (3) HSC differentiation was verified by reduced SSEA1 expression and increased CD117 and Sca1 expression. (4) All the effects caused by HSC-EXs were accompanied by significant reduction of Notch1 and Hes1 expression, thus inhibition of the Notch1/Hes1 pathway, whereas activation of Notch by Jagged1 abolished the effects of HSC-EXs . In conclusion, HSC-EXs promote hematopoietic differentiation of mouse ESCs in vitro by inhibiting the miR126/Notch1 pathway.