Mesenchymal stem cells as therapeutic tools and gene carriers in liver fibrosis and hepatocellular carcinoma

被引:69
作者
Aquino, J. B. [1 ,2 ]
Bolontrade, M. F. [2 ,3 ]
Garcia, M. G. [1 ,2 ]
Podhajcer, O. L. [2 ,3 ]
Mazzolini, G. [1 ,2 ]
机构
[1] Austral Univ, Gene Therapy Lab, Liver Univ Sch Med, Buenos Aires, DF, Argentina
[2] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
[3] Fdn Inst Leloir, Mol & Cellular Therapy Lab, Buenos Aires, DF, Argentina
关键词
liver cirrhosis; mesenchymal stromal cells; adult stem cells; chemotaxis; HEPATIC STELLATE CELLS; HUMAN BONE-MARROW; HEPATOCYTE GROWTH-FACTOR; STROMAL CELLS; IN-VITRO; PROGENITOR CELLS; PERIPHERAL-BLOOD; UMBILICAL-CORD; ADIPOSE-TISSUE; TUMOR STROMA;
D O I
10.1038/gt.2010.10
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mesenchymal stem (stromal) cells (MSCs) are a source of circulating progenitors that are able to generate cells of all mesenchymal lineages and to cover cellular demands of injured tissues. The extent of their transdifferentiation plasticity remains controversial. Cells with MSC properties have been obtained from diverse tissues after purification and expansion in vitro. These cellular populations are heterogeneous and under certain conditions show pluripotent-like properties. MSCs present immunosuppressive and anti-inflammatory features and high migratory capacity toward inflamed or remodeling tissues. In this study we review available data regarding factors and signaling axes involved in the chemoattraction and engraftment of MSCs to an injured tissue or to a tissue undergoing active remodeling. Moreover, experimental evidence in support of uses of MSCs as vehicles of therapeutic genes is discussed. Because of its regenerative capacity and its particular immune properties, the liver is a good model to analyze the potential of MSC-based therapies. Finally, the potential application of MSCs and genetically modified MSCs in liver fibrosis and hepatocellular carcinoma (HCC) is proposed in view of available evidence. Gene Therapy (2010) 17, 692-708; doi: 10.1038/gt.2010.10; published online 11 March 2010
引用
收藏
页码:692 / 708
页数:17
相关论文
共 271 条
  • [1] Human mesenchymal stem cells modulate allogeneic immune cell responses
    Aggarwal, S
    Pittenger, MF
    [J]. BLOOD, 2005, 105 (04) : 1815 - 1822
  • [2] Toll-like receptor signalling
    Akira, S
    Takeda, K
    [J]. NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) : 499 - 511
  • [3] Stem cells in liver regeneration, fibrosis and cancer: the good, the bad and the ugly
    Alison, M. R.
    Islam, S.
    Lim, S.
    [J]. JOURNAL OF PATHOLOGY, 2009, 217 (02) : 282 - 298
  • [4] LacZ and interleukin-3 expression in vivo after retroviral transduction of marrow-derived human osteogenic mesenchymal progenitors
    Allay, JA
    Dennis, JE
    Haynesworth, SE
    Majumdar, MK
    Clapp, DW
    Shultz, LD
    Caplan, AI
    Gerson, SL
    [J]. HUMAN GENE THERAPY, 1997, 8 (12) : 1417 - 1427
  • [5] Can stem cells cross lineage boundaries?
    Anderson, DJ
    Gage, FH
    Weissman, IL
    [J]. NATURE MEDICINE, 2001, 7 (04) : 393 - 395
  • [6] HUMAN GENE-THERAPY
    ANDERSON, WF
    [J]. SCIENCE, 1992, 256 (5058) : 808 - 813
  • [7] Nonhematopoietic/endothelial SSEA-1+ cells define the most primitive progenitors in the adult murine bone marrow mesenchymal compartment
    Anjos-Afonso, Fernando
    Bonnet, Dominique
    [J]. BLOOD, 2007, 109 (03) : 1298 - 1306
  • [8] Enhanced Liver Regeneration Following Changes Induced by Hepatocyte-Specific Genetic Ablation of Integrin-Linked Kinase
    Apte, Udayan
    Gkretsi, Vasiliki
    Bowen, William C.
    Mars, Wendy M.
    Luo, Jian-Hua
    Donthamsetty, Shashikiran
    Orr, Ann
    Monga, Satdarshan P. S.
    Wu, Chuanyue
    Michalopoulos, George K.
    [J]. HEPATOLOGY, 2009, 50 (03) : 844 - 851
  • [9] CD44 IS THE PRINCIPAL CELL-SURFACE RECEPTOR FOR HYALURONATE
    ARUFFO, A
    STAMENKOVIC, I
    MELNICK, M
    UNDERHILL, CB
    SEED, B
    [J]. CELL, 1990, 61 (07) : 1303 - 1313
  • [10] Isolation of putative progenitor endothelial cells for angiogenesis
    Asahara, T
    Murohara, T
    Sullivan, A
    Silver, M
    vanderZee, R
    Li, T
    Witzenbichler, B
    Schatteman, G
    Isner, JM
    [J]. SCIENCE, 1997, 275 (5302) : 964 - 967