Conditioned media derived from mesenchymal stem cell cultures: The next generation for regenerative medicine

被引:116
作者
Gunawardena, Tarini Nawamalie Abeysinghe [1 ]
Rahman, Mohammad Tariqur [1 ]
Abdullah, Basri Johan Jeet [2 ]
Abu Kasim, Noor Hayaty [1 ,3 ]
机构
[1] Univ Malaya, Dept Restorat Dent, Fac Dent, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Dept Biomed Imaging, Fac Med, Kuala Lumpur, Malaysia
[3] Univ Malaya, Regenerat Dent Res Grp, Fac Dent, Kuala Lumpur, Malaysia
关键词
conditioned media; mesenchymal stem cells; paracrine factors; paracrine signalling; regenerative medicine; secretome; MARROW STROMAL CELLS; TRAUMATIC BRAIN-INJURY; BONE-MARROW; IN-VITRO; ISCHEMIC-HEART; RAT MODEL; OSTEOGENIC DIFFERENTIATION; PARACRINE MECHANISMS; PERIPHERAL-BLOOD; THERAPY;
D O I
10.1002/term.2806
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Recent studies suggest that the main driving force behind the therapeutic activity observed in mesenchymal stem cells (MSCs) are the paracrine factors secreted by these cells. These biomolecules also trigger antiapoptotic events to prevent further degeneration of the diseased organ through paracrine signalling mechanisms. In comparison with the normal physiological conditions, an increased paracrine gradient is observed within the peripheral system of diseased organs that enhances the migration of tissue-specific MSCs towards the site of infection or injury to promote healing. Thus, upon administration of conditioned media derived from mesenchymal stem cell cultures (MSC-CM) could contribute in maintaining the increased paracrine factor gradient between the diseased organ and the stem cell niche in order to speed up the process of recovery. Based on the principle of the paracrine signalling mechanism, MSC-CM, also referred as the secretome of the MSCs, is a rich source of the paracrine factors and are being studied extensively for a wide range of regenerative therapies such as myocardial infarction, stroke, bone regeneration, hair growth, and wound healing. This article highlights the current technological applications and advances of MSC-CM with the aim to appraise its future potential as a regenerative therapeutic agent.
引用
收藏
页码:569 / 586
页数:18
相关论文
共 132 条
[1]   Stem cell-conditioned medium accelerates distraction osteogenesis through multiple regenerative mechanisms [J].
Ando, Yuji ;
Matsubara, Kohki ;
Ishikawa, Jun ;
Fujio, Masahito ;
Shohara, Ryutaro ;
Hibi, Hideharu ;
Ueda, Minoru ;
Yamamoto, Akihito .
BONE, 2014, 61 :82-90
[2]  
Ashiba K., 2015, INFLAMM REGEN, V35, P57, DOI [10.2492/inflammregen.35.057, DOI 10.2492/inflammregen.35.057]
[3]   Osteogenic differentiation of noncultured immunoisolated bone marrow-derived CD105+ cells [J].
Aslan, Hadi ;
Zilberman, Yoram ;
Kandel, Leonid ;
Liebergall, Meir ;
Oskouian, Rod J. ;
Gazit, Dan ;
Gazit, Zulma .
STEM CELLS, 2006, 24 (07) :1728-1737
[4]  
Augello A, 2010, EUR CELLS MATER, V20, P121
[5]   Mesenchymal stem cell secreted vesicles provide novel opportunities in (stem) cell-free therapy [J].
Baglio, Serena Rubina ;
Pegtel, D. Michiel ;
Baldini, Nicola .
FRONTIERS IN PHYSIOLOGY, 2012, 3
[6]   Stem cell differentiation requires a paracrine pathway in the heart [J].
Behfar, A ;
Zingman, LV ;
Hodgson, DM ;
Rauzier, JM ;
Kane, GC ;
Terzic, A ;
Pucéat, M .
FASEB JOURNAL, 2002, 16 (12) :1558-1566
[7]   Efficacious and Clinically Relevant Conditioned Medium of Human Adipose-derived Stem Cells for Therapeutic Angiogenesis [J].
Bhang, Suk Ho ;
Lee, Seahyoung ;
Shin, Jung-Youn ;
Lee, Tae-Jin ;
Jang, Hyeon-Ki ;
Kim, Byung-Soo .
MOLECULAR THERAPY, 2014, 22 (04) :862-872
[8]   Mesenchymal Stem Cells Secrete Multiple Cytokines That Promote Angiogenesis and Have Contrasting Effects on Chemotaxis and Apoptosis [J].
Boomsma, Robert A. ;
Geenen, David L. .
PLOS ONE, 2012, 7 (04) :e35685
[9]   MESENCHYMAL STEM-CELLS IN IN BONE-DEVELOPMENT, BONE REPAIR, AND SKELETAL REGENERATION THERAPY [J].
BRUDER, SP ;
FINK, DJ ;
CAPLAN, AI .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 56 (03) :283-294
[10]   Brain-derived neurotrophic factor regulates the onset and severity of motor dysfunction associated with enkephalinergic neuronal degeneration in Huntington's disease [J].
Canals, JM ;
Pineda, JR ;
Torres-Peraza, JF ;
Bosch, M ;
Martín-Ibañez, R ;
Muñoz, MT ;
Mengod, G ;
Ernfors, P ;
Alberch, J .
JOURNAL OF NEUROSCIENCE, 2004, 24 (35) :7727-7739