The Role of Microvesicles Derived from Mesenchymal Stem Cells in Lung Diseases

被引:65
作者
Chen, Jie [1 ]
Li, Chonghui [2 ,3 ]
Chen, Liangan [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Chinese Peoples Liberat Army Med Coll, Dept Resp Med, Beijing, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Med Coll, Dept Hepatobiliary Surg, Beijing 100853, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Chinese PLAMed Coll, Inst Hepatobiliary Surg, Beijing 100853, Peoples R China
关键词
HORIZONTAL TRANSFER; STROMAL CELLS; INJURY; DELIVERY; MARROW; VESICLES; MICE;
D O I
10.1155/2015/985814
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Microvesicles (MVs) are membrane vesicles that are released by many types of cells and have recently been considered important mediators of cell-to-cell communication. MVs serve as a vehicle to transfer proteins and messenger RNA and microRNA (miRNA) to distant cells, which alters the gene expression, proliferation, and differentiation of the recipient cells. Several studies have demonstrated that mesenchymal stem cells (MSCs) have the capacity to reverse acute and chronic lung injury in different experimental models through paracrine mechanisms. This paracrine action may be partially accounted for by MVs that are derived from MSCs. MSC-derived MVs may confer a stem cell-like phenotype to injured cells with the consequent activation of self-regenerative programmers. In this review, we summarize the characteristics and biological activities of MSC-derived MVs, and we describe their potential in novel therapeutic approaches in regenerative medicine to repair damaged tissues. Additionally, we provide an overview of studies that have assessed the role of MSC-derived MVs in lung diseases, including the mechanisms that may account for their therapeutic potential. Finally, we discuss the clinical use of MSC-derived MVs with several suggestions for enhancing their therapeutic efficiency.
引用
收藏
页数:6
相关论文
共 43 条
[1]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[2]  
[Anonymous], 2012, FRONTIERS PHYSL
[3]   Modulation of monocyte-endothelial cell interactions by platelet microparticles [J].
Barry, OP ;
Praticò, D ;
Savani, RC ;
FitzGerald, GA .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (01) :136-144
[4]   Therapeutic potential of mesenchymal stem cell-derived microvesicles [J].
Biancone, Luigi ;
Bruno, Stefania ;
Deregibus, Maria Chiara ;
Tetta, Ciro ;
Camussi, Giovanni .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2012, 27 (08) :3037-3042
[5]   Microvesicles Derived from Mesenchymal Stem Cells Enhance Survival in a Lethal Model of Acute Kidney Injury [J].
Bruno, Stefania ;
Grange, Cristina ;
Collino, Federica ;
Deregibus, Maria Chiara ;
Cantaluppi, Vincenzo ;
Biancone, Luigi ;
Tetta, Ciro ;
Camussi, Giovanni .
PLOS ONE, 2012, 7 (03)
[6]   Role of mesenchymal stem cell-derived microvesicles in tissue repair [J].
Bruno, Stefania ;
Camussi, Giovanni .
PEDIATRIC NEPHROLOGY, 2013, 28 (12) :2249-2254
[7]   Mesenchymal Stem Cell-Derived Microvesicles Protect Against Acute Tubular Injury [J].
Bruno, Stefania ;
Grange, Cristina ;
Deregibus, Maria Chiara ;
Calogero, Raffaele A. ;
Saviozzi, Silvia ;
Collino, Federica ;
Morando, Laura ;
Busca, Alessandro ;
Falda, Michele ;
Bussolati, Benedetta ;
Tetta, Ciro ;
Camussi, Giovanni .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2009, 20 (05) :1053-1067
[8]   Role of stem-cell-derived microvesicles in the paracrine action of stem cells [J].
Camussi, Giovanni ;
Deregibus, Maria Chiara ;
Cantaluppi, Vincenzo .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2013, 41 :283-287
[9]   Exosomes/microvesicles as a mechanism of cell-to-cell communication [J].
Camussi, Giovanni ;
Deregibus, Maria C. ;
Bruno, Stefania ;
Cantaluppi, Vincenzo ;
Biancone, Luigi .
KIDNEY INTERNATIONAL, 2010, 78 (09) :838-848
[10]   Antigen-presenting property of mesenchymal stem cells occurs during a narrow window at low levels of interferon-γ [J].
Chan, Jennifer L. ;
Tang, Katherine C. ;
Patel, Anoop P. ;
Bonilla, Larissa M. ;
Pierobon, Nicola ;
Ponzio, Nicholas M. ;
Rameshwar, Pranela .
BLOOD, 2006, 107 (12) :4817-4824