Exosomes derived from mineralizing osteoblasts promote ST2 cell osteogenic differentiation by alteration of microRNA expression

被引:327
作者
Cui, Yazhou [1 ]
Luan, Jing [1 ]
Li, Haiying [1 ]
Zhou, Xiaoyan [1 ]
Han, Jinxiang [1 ]
机构
[1] Minist Hlth, Shandong Acad Med Sci, Shandong Med Biotechnol Ctr, Key Lab Biotechnol Drugs, Jinan 250062, Peoples R China
基金
中国国家自然科学基金;
关键词
cell-to-cell communication; exosomes; microRNA; osteoblast differentiation; MESENCHYMAL STEM-CELLS; MEDIATED TRANSFER; MECHANISMS;
D O I
10.1002/1873-3468.12024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Mineralizing osteoblasts (MOBs) can release exosomes, although the functional significance remains unclear. In the present study, we demonstrate that exosomes derived from mineralizing pre-osteoblast MC3T3-E1 cells can promote bone marrow stromal cell (ST2) differentiation to osteoblasts. We reveal that MOB-derived exosomes significantly influence miRNA profiles in recipient ST2 cells, and these changes tend to activate the Wnt signaling pathway by inhibiting Axin1 expression and increasing -catenin expression. We also suggest that MOB derived-exosomes partly induce the variation in miRNA expression in recipient ST2 cells by exosomal miRNA transfer. These findings suggest an exosome-mediated mode of cell-to-cell communication in the osteogenic microenvironment, and also indicate the potential of MOB exosomes in bone tissue engineering.
引用
收藏
页码:185 / 192
页数:8
相关论文
共 18 条
[1]
OSTEOGENIC DIFFERENTIATION OF MESENCHYMAL STEM CELLS IS REGULATED BY OSTEOCYTE AND OSTEOBLAST CELLS IN A SIMPLIFIED BONE NICHE [J].
Birmingham, E. ;
Niebur, G. L. ;
McHugh, P. E. ;
Shaw, G. ;
Barry, F. P. ;
McNamara, L. M. .
EUROPEAN CELLS & MATERIALS, 2012, 23 :13-27
[2]
Quantitative and stoichiometric analysis of the microRNA content of exosomes [J].
Chevillet, John R. ;
Kang, Qing ;
Ruf, Ingrid K. ;
Briggs, Hilary A. ;
Vojtech, Lucia N. ;
Hughes, Sean M. ;
Cheng, Heather H. ;
Arroyo, Jason D. ;
Meredith, Emily K. ;
Gallichotte, Emily N. ;
Pogosova-Agadjanyan, Era L. ;
Morrissey, Colm ;
Stirewalt, Derek L. ;
Hladik, Florian ;
Yu, Evan Y. ;
Higano, Celestia S. ;
Tewari, Muneesh .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (41) :14888-14893
[3]
Co-culture of canine mesenchymal stem cells with primary bone-derived osteoblasts promotes osteogenic differentiation [J].
Csaki, C. ;
Matis, U. ;
Mobasheri, A. ;
Shakibaei, M. .
HISTOCHEMISTRY AND CELL BIOLOGY, 2009, 131 (02) :251-266
[4]
Conditioned medium from osteocytes stimulates the proliferation of bone marrow mesenchymal stem cells and their differentiation into ostcoblasts [J].
Heino, TJ ;
Hentunen, TA ;
Väänänen, HK .
EXPERIMENTAL CELL RESEARCH, 2004, 294 (02) :458-468
[5]
Mechanisms of RNA loading into exosomes [J].
Janas, Teresa ;
Janas, Maja M. ;
Sapon, Karolina ;
Janas, Tadeusz .
FEBS LETTERS, 2015, 589 (13) :1391-1398
[6]
Jiang C, 2014, EVID-BASED COMPL ALT, V2014
[7]
Wnt/β-Catenin Signaling: Components, Mechanisms, and Diseases [J].
MacDonald, Bryan T. ;
Tamai, Keiko ;
He, Xi .
DEVELOPMENTAL CELL, 2009, 17 (01) :9-26
[8]
Carcinoma-derived exosomes modify microenvironment [J].
Maitland, Norman J. .
ONCOTARGET, 2015, 6 (03) :1344-1345
[9]
Mesenchymal-stem-cell-derived exosomes accelerate skeletal muscle regeneration [J].
Nakamura, Yoshihiro ;
Miyaki, Shigeru ;
Ishitobi, Hiroyuki ;
Matsuyama, Sho ;
Nakasa, Tomoyuki ;
Kamei, Naosuke ;
Akimoto, Takayuki ;
Higashi, Yukihito ;
Ochi, Mitsuo .
FEBS LETTERS, 2015, 589 (11) :1257-1265
[10]
Microvesicles and exosomes for intracardiac communication [J].
Sluijter, Joost P. G. ;
Verhage, Vera ;
Deddens, Janine C. ;
van den Akker, Frederieke ;
Doevendans, Pieter A. .
CARDIOVASCULAR RESEARCH, 2014, 102 (02) :302-311