Mesenchymal Stem Cells on Horizon: A New Arsenal of Therapeutic Agents

被引:71
作者
Abbasi-Malati, Zahra [1 ,2 ]
Roushandeh, Amaneh Mohammadi [2 ]
Kuwahara, Yoshikazu [3 ]
Roudkenar, Mehryar Habibi [4 ]
机构
[1] High Inst Res & Educ Transfus Med, Blood Transfus Res Ctr, Tehran, Iran
[2] Guilan Univ Med Sci, Paramed Fac, Med Biotechnol Res Ctr, Rasht, Iran
[3] Tohoku Med & Pharmaceut Univ, Div Radiat Biol & Med, Fac Med, Sendai, Miyagi, Japan
[4] Guilan Univ Med Sci, Cardiovasc Dis Res Ctr, Dept Cardiol, Heshmat Hosp,Sch Med, Rasht, Iran
关键词
MSC; Secretome; Cell-free therapy; Condition medium; Therapeutic agents; REGULATORY DENDRITIC CELLS; MARROW STROMAL CELLS; VERSUS-HOST-DISEASE; CONDITIONED MEDIUM; IN-VITRO; BONE; EXOSOMES; SECRETOME; MICROVESICLES; PROTECT;
D O I
10.1007/s12015-018-9817-x
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Over 10 years, mesenchymal stem cells (MSCs) have been considered as valuable and suitable cells for cell-based therapy applications, particularly in clinical trials. In any case, they are as yet not utilized routinely in clinics. At first, it was believed that MSCs play their roles, especially in regenerative medicine due to their differentiation and cell replacement properties. Interestingly, it is well-known that MSCs mainly exert their therapeutic effects through their vast bioactive factors. These findings turned scientists' consideration toward cell-free therapy concepts. From this point of view, MSCs can be considered as an arsenal of natural bioreactors in variety of therapeutic agents. MSCs inherently express various important therapeutic agents such as growth factors and cytokines that can be manufactured, handled and stored as a prepared-to-go biologic product. In this review, we provide a vision, highlight as well as discuss in order to introduce competitive natural robust bioreactor MSCs on the horizon.
引用
收藏
页码:484 / 499
页数:16
相关论文
共 142 条
[21]
Anti-inflammatory protein TSG-6 secreted by activated MSCs attenuates zymosan-induced mouse peritonitis by decreasing TLR2/NF-κB signaling in resident macrophages [J].
Choi, Hosoon ;
Lee, Ryang Hwa ;
Bazhanov, Nikolay ;
Oh, Joo Youn ;
Prockop, Darwin J. .
BLOOD, 2011, 118 (02) :330-338
[22]
Choi M, 2014, MOL CELLS, V37, P133
[23]
Novel Cell-Free Strategy for Therapeutic Angiogenesis: In Vitro Generated Conditioned Medium Can Replace Progenitor Cell Transplantation [J].
Di Santo, Stefano ;
Yang, Zijiang ;
von Ballmoos, Moritz Wyler ;
Voelzmann, Jan ;
Diehm, Nicolas ;
Baumgartner, Iris ;
Kalka, Christoph .
PLOS ONE, 2009, 4 (05)
[24]
Mesenchymal Stem Cells [J].
Ding, Dah-Ching ;
Shyu, Woei-Cherng ;
Lin, Shinn-Zong .
CELL TRANSPLANTATION, 2011, 20 (01) :5-14
[25]
Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement [J].
Dominici, M. ;
Le Blanc, K. ;
Mueller, I. ;
Slaper-Cortenbach, I. ;
Marini, F. C. ;
Krause, D. S. ;
Deans, R. J. ;
Keating, A. ;
Prockop, D. J. ;
Horwitz, E. M. .
CYTOTHERAPY, 2006, 8 (04) :315-317
[26]
Mesenchymal stem cell-conditioned medium reduces liver injury and enhances regeneration in reduced-size rat liver transplantation [J].
Du, Zhiyong ;
Wei, Cuifeng ;
Cheng, Kun ;
Han, Baosan ;
Yan, Jiqi ;
Zhang, Mingjun ;
Peng, Chenghong ;
Liu, Yingbin .
JOURNAL OF SURGICAL RESEARCH, 2013, 183 (02) :907-915
[27]
Importance of Serum Source for the In Vitro Replicative Senescence of Human Bone Marrow Derived Mesenchymal Stem Cells [J].
Duggal, Shivali ;
Brinchmann, Jan E. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2011, 226 (11) :2908-2915
[28]
The human cathelicidin antimicrobial peptide LL-37 as a potential treatment for polymicrobial infected wounds [J].
Duplantier, Allen J. ;
van Hoek, Monique L. .
FRONTIERS IN IMMUNOLOGY, 2013, 4
[29]
Potential therapeutic effect of the secretome from human uterine cervical stem cells against both cancer and stromal cells compared with adipose tissue stem cells [J].
Eiro, Noemi ;
Sendon-Lago, Juan ;
Seoane, Samuel ;
Bermudez, Maria A. ;
Lamelas, Maria Luz ;
Garcia-Caballero, Tomas ;
Schneider, Jose ;
Perez-Fernandez, Roman ;
Vizoso, Francisco J. .
ONCOTARGET, 2014, 5 (21) :10692-10708
[30]
Murine mesenchymal stem cells suppress dendritic cell migration, maturation and antigen presentation [J].
English, Karen ;
Barry, Frank P. ;
Mahon, Bernard P. .
IMMUNOLOGY LETTERS, 2008, 115 (01) :50-58