Mesenchymal stem cell therapy for the treatment of traumatic brain injury: progress and prospects

被引:100
作者
Das, Mahasweta [1 ,2 ]
Mayilsamy, Karthick [1 ,2 ]
Mohapatra, Shyam S. [1 ,3 ]
Mohapatra, Subhra [1 ,2 ]
机构
[1] James A Haley Vet Hosp, Tampa, FL 33612 USA
[2] Univ S Florida, Coll Med, Dept Mol Med, Tampa, FL 33612 USA
[3] Univ S Florida, Coll Med, Dept Internal Med, Tampa, FL 33612 USA
关键词
exosomes; mesenchymal stem cell (MSC); regenerative medicine; traumatic brain injury (TBI); MARROW STROMAL CELLS; T-LYMPHOCYTE PROLIFERATION; MURINE BONE-MARROW; FUNCTIONAL RECOVERY; SPINAL-CORD; NEUROVASCULAR PLASTICITY; EXTRACELLULAR VESICLES; INTERNATIONAL-SOCIETY; INTRANASAL DELIVERY; COMPUTED-TOMOGRAPHY;
D O I
10.1515/revneuro-2019-0002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Traumatic brain injury (TBI) is a major cause of injury-related mortality and morbidity in the USA and around the world. The survivors may suffer from cognitive and memory deficits, vision and hearing loss, movement disorders, and different psychological problems. The primary insult causes neuronal damage and activates astrocytes and microglia which evokes immune responses causing further damage to the brain. Clinical trials of drugs to recover the neuronal loss are not very successful. Regenerative approaches for TBI using mesenchymal stem cells (MSCs) seem promising. Results of preclinical research have shown that transplantation of MSCs reduced secondary neurodegeneration and neuroinflammation, promoted neurogenesis and angiogenesis, and improved functional outcome in the experimental animals. The functional improvement is not necessarily related to cell engraftment; rather, immunomodulation by molecular factors secreted by MSCs is responsible for the beneficial effects of this therapy. However, MSC therapy has a few drawbacks including tumor formation, which can be avoided by the use of MSC-derived exosomes. This review has focused on the research works published in the field of regenerative therapy using MSCs after TBI and its future direction.
引用
收藏
页码:839 / 855
页数:17
相关论文
共 191 条
[1]   Transporting therapeutics across the blood-brain barrier [J].
Abbott, NJ ;
Romero, IA .
MOLECULAR MEDICINE TODAY, 1996, 2 (03) :106-113
[2]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[3]   Transplanted Neurally Modified Bone Marrow-Derived Mesenchymal Stem Cells Promote Tissue Protection and Locomotor Recovery in Spinal Cord Injured Rats [J].
Alexanian, Arshak R. ;
Fehlings, Michael G. ;
Zhang, Zhiying ;
Maiman, Dennis J. .
NEUROREHABILITATION AND NEURAL REPAIR, 2011, 25 (09) :873-880
[4]   Immune function of microglia [J].
Aloisi, F .
GLIA, 2001, 36 (02) :165-179
[5]   A link between the accumulation of DNA damage and loss of multi-potency of human mesenchymal stromal cells [J].
Alves, Hugo ;
Munoz-Najar, Ursula ;
de Wit, Jan ;
Renard, Auke J. S. ;
Hoeijmakers, Jan H. J. ;
Sedivy, John M. ;
van Blitterswijk, Clemens ;
de Boer, Jan .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2010, 14 (12) :2729-2738
[6]  
[Anonymous], 2012, Drug Discov Today Technol, V9, pe71, DOI 10.1016/j.ddtec.2011.12.002
[7]   The Role of Reactive Oxygen Species in Mesenchymal Stem Cell Adipogenic and Osteogenic Differentiation: A Review [J].
Atashi, Fatemeh ;
Modarressi, Ali ;
Pepper, Michael S. .
STEM CELLS AND DEVELOPMENT, 2015, 24 (10) :1150-1163
[8]   Characterization of mesenchymal stem cells isolated from murine bone marrow by negative selection [J].
Baddoo, M ;
Hill, K ;
Wilkinson, R ;
Gaupp, D ;
Hughes, C ;
Kopen, GC ;
Phinney, DG .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 89 (06) :1235-1249
[9]   Treatment of chronic wounds with bone marrow-derived cells [J].
Badiavas, EV ;
Falanga, V .
ARCHIVES OF DERMATOLOGY, 2003, 139 (04) :510-516
[10]   Isolation, selection and culture methods to enhance clonogenicity of mouse bone marrow derived mesenchymal stromal cell precursors [J].
Baustian, Claas ;
Hanley, Shirley ;
Ceredig, Rhodri .
STEM CELL RESEARCH & THERAPY, 2015, 6