Therapeutic potential of human olfactory bulb neural stem cells for spinal cord injury in rats

被引:11
作者
Marei, H. E. [1 ]
Althani, A. [2 ]
Rezk, S. [3 ]
Farag, A. [3 ]
Lashen, S. [3 ]
Afifi, N. [4 ]
Abd-Elmaksoud, A. [3 ]
Pallini, R. [5 ]
Casalbore, P. [6 ]
Cenciarelli, C. [7 ]
Caceci, T. [8 ]
机构
[1] Qatar Univ, Biomed Res Ctr, Doha 2713, Qatar
[2] Qatar Univ, Dept Hlth Sci, Coll Arts & Sci, Doha, Qatar
[3] Mansoura Univ, Dept Cytol & Histol, Fac Vet Med, Mansoura, Egypt
[4] Ain Shams Univ, Dept Anat, Fac Med, Cairo, Egypt
[5] Univ Cattolica Sacro Cuore, Inst Neurosurg, Rome, Italy
[6] Natl Res Council Italy, Inst Cell Biol & Neurobiol, Rome, Italy
[7] Natl Res Council Italy, Inst Translat Pharmacol, Rome, Italy
[8] Virginia Polytech Inst & State Univ, Dept Biomed Sci, Virginia Mareland Reg Coll Vet Med, Blacksburg, VA 24061 USA
关键词
TRANSCRIPTION FACTORS; PARKINSONS-DISEASE; AXON REGENERATION; PRECURSOR CELLS; IN-VITRO; DIFFERENTIATION; TRANSPLANTATION; RECOVERY; PROMOTES; SURVIVAL;
D O I
10.1038/sc.2016.14
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study design: Adult human olfactory bulb neural stem cells (OBNSCs) were isolated from human patients undergoing craniotomy for tumor resection. They were genetically engineered to overexpresses green fluorescent protein (GFP) to help trace them following engraftment. Spinal cord injury (SCI) was induced in rats using standard laminectomy protocol, and GFP-OBNSC were engrafted into rat model of SCI at day 7 post injury. Three rat groups were used: (i) Control group, (ii) Sham group (injected with cerebrospinal fluid) and treated group (engrafted with OBNSCs). Tissues from different groups were collected weekly up to 2 months. The collected tissues were fixed in 4% paraformaldehyde, processed for paraffin sectioning, immunohistochemically stained for different neuronal and glial markers and examined with bright-field fluorescent microscopy. Restoration of sensory motor functions we assessed on a weekly bases using the BBB score. Objectives: To assess the therapeutic potential of OBNSCs-GFP and their ability to survive, proliferate, differentiate and to restore lost sensory motor functions following their engraftment in spinal cord injury (SCI). Methods: GFP-OBNSC were engrafted into a rat model of SCI at day 7 post injury and were followed-up to 8 weeks using behavioral and histochemical methods. Results: All transplanted animals exhibited successful engraftment. The survival rate was about 30% of initially transplanted cells. Twenty-seven percent of the engrafted cells differentiated along the NG2 and O4-positive oligodendrocyte lineage, 16% into MAP2 and beta-tubulin-positive neurons, and 56% into GFAP-positive astrocytes. Conclusion: GFP-OBNSCs had survived for >8 weeks after engraftment and were differentiated into neurons, astrocytes and oligodendrocytes, The engrafted cells were distributed throughout gray and white matter of the cord with no evidence of abnormal morphology or any mass formation indicative of tumorigenesis. However, the engrafted cells failed to restore lost sensory and motor functions as evident from behavioral analysis using the BBB score test.
引用
收藏
页码:785 / 797
页数:13
相关论文
共 50 条
[1]  
Bambakidis Nicholas C, 2004, Spine J, V4, P16, DOI 10.1016/j.spinee.2003.07.004
[2]   A SENSITIVE AND RELIABLE LOCOMOTOR RATING-SCALE FOR OPEN-FIELD TESTING IN RATS [J].
BASSO, DM ;
BEATTIE, MS ;
BRESNAHAN, JC .
JOURNAL OF NEUROTRAUMA, 1995, 12 (01) :1-21
[3]   Graded histological and locomotor outcomes after spinal cord contusion using the NYU weight-drop device versus transection [J].
Basso, DM ;
Beattie, MS ;
Bresnahan, JC .
EXPERIMENTAL NEUROLOGY, 1996, 139 (02) :244-256
[4]   Neural stem cells implanted into MPTP-treated monkeys increase the size of endogenous tyrosine hydroxylase-positive cells found in the striatum: A return to control measures [J].
Bjugstad, KB ;
Redmond, DE ;
Teng, YD ;
Elsworth, JD ;
Roth, RH ;
Blanchard, BC ;
Snyder, EY ;
Sladek, JR .
CELL TRANSPLANTATION, 2005, 14 (04) :183-192
[5]   Human neural stem cells migrate along the nigrostriatal pathway in a primate model of Parkinson's disease [J].
Bjugstad, Kimberly B. ;
Teng, Yang D. ;
Redmond, D. Eugene, Jr. ;
Elsworth, John D. ;
Roth, Robert H. ;
Cornelius, Shannon K. ;
Snyder, Evan Y. ;
Sladek, John R., Jr. .
EXPERIMENTAL NEUROLOGY, 2008, 211 (02) :362-369
[6]   Experimental traumatic brain injury modulates the survival migration, and terminal phenotype of transplanted epidermal growth factor receptor-activated neural stem cells [J].
Boockvar, JA ;
Schouten, J ;
Royo, N ;
Millard, M ;
Spangler, Z ;
Castelbuono, D ;
Snyder, E ;
O'Rourke, D ;
McIntosh, T .
NEUROSURGERY, 2005, 56 (01) :163-171
[7]  
Braga-Silva Jefferson, 2007, Acta ortop. bras., V15, P155
[8]   Pluripotent stem cells engrafted into the normal or lesioned adult rat spinal cord are restricted to a glial lineage [J].
Cao, QL ;
Zhang, YP ;
Howard, RM ;
Walters, WM ;
Tsoulfas, P ;
Whittemore, SR .
EXPERIMENTAL NEUROLOGY, 2001, 167 (01) :48-58
[9]   Stem cell repair of central nervous system injury [J].
Cao, QL ;
Benton, RL ;
Whittemore, SR .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 68 (05) :501-510
[10]   Differentiation of engrafted neuronal-restricted precursor cells is inhibited in the traumatically injured spinal cord [J].
Cao, QL ;
Howard, RM ;
Dennison, JB ;
Whittemore, SR .
EXPERIMENTAL NEUROLOGY, 2002, 177 (02) :349-359