Intraventricular Injection of Human Dental Pulp Stem Cells Improves Hypoxic-Ischemic Brain Damage in Neonatal Rats

被引:48
作者
Fang, Cheng-zhi [1 ,2 ]
Yang, Yu-jia [1 ]
Wang, Qin-hong [1 ]
Yao, Yue [1 ]
Zhang, Xiao-ying [1 ]
He, Xue-hua [1 ]
机构
[1] Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China
[2] Wuhan Childrens Hosp, Dept Neonatol, Wuhan, Peoples R China
关键词
THERAPY;
D O I
10.1371/journal.pone.0066748
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective: To investigate the effect of intraventricular injection of human dental pulp stem cells (DPSCs) on hypoxic-ischemic brain damage (HIBD) in neonatal rats. Methods: Thirty-six neonatal rats (postnatal day 7) were assigned to control, HIBD, or HIBD+DPSC groups (n = 12 each group). For induction of HIBD, rats underwent left carotid artery ligation and were exposed to 8% to 10% oxygen for 2 h. Hoechst 33324-labeled human DPSCs were injected into the left lateral ventricle 3 days after HIBD. Behavioral assays were performed to assess hypoxic-ischemic encephalopathy (HIE), and on postnatal day 45, DPSC survival was assessed and expression of neural and glial markers was evaluated by immunohistochemistry and Western blot. Results: The HIBD group showed significant deficiencies compared to control on T-maze, radial water maze, and postural reflex tests, and the HIBD+DPSC group showed significant improvement on all behavioral tests. On postnatal day 45, Hoechst 33324-labeled DPSC nuclei were visible in the injected region and left cortex. Subsets of DPSCs showed immunostaining for neuronal (neuron-specific enolase [NSE], Nestin) and glial markers (glial fibrillary acidic protein [GFAP], O4). Significantly decreased staining/expression for NSE, GFAP, and O4 was found in the HBID group compared to control, and this was significantly increased in the HBID+DPSC group. Conclusion: Intraventricular injection of human DPSCs improves HIBD in neonatal rats.
引用
收藏
页数:7
相关论文
共 14 条
[1]   The neuroprotective effect of dental pulp cells in models of Alzheimer's and Parkinson's disease [J].
Apel, C. ;
Forlenza, O. V. ;
Paula, V. J. R. de ;
Talib, L. L. ;
Denecke, B. ;
Eduardo, C. P. ;
Gattaz, W. F. .
JOURNAL OF NEURAL TRANSMISSION, 2009, 116 (01) :71-78
[2]   Adult human dental pulp stem cells differentiate toward functionally active neurons under appropriate environmental cues [J].
Arthur, Agnes ;
Rychkov, Grigori ;
Shi, Songtao ;
Koblar, Simon Andrea ;
Gronthos, Stan .
STEM CELLS, 2008, 26 (07) :1787-1795
[3]   Cell therapy for neonatal hypoxia-ischemia and cerebral palsy [J].
Bennet, Laura ;
Tan, Sidhartha ;
Van den Heuij, Lotte ;
Derrick, Matthew ;
Groenendaal, Floris ;
van Bel, Frank ;
Juul, Sandra ;
Back, Stephen A. ;
Northington, Frances ;
Robertson, Nicola J. ;
Mallard, Carina ;
Gunn, Alistair Jan .
ANNALS OF NEUROLOGY, 2012, 71 (05) :589-600
[4]   Sensorimotor function and neuropathology five to six weeks after hypoxia-ischemia in seven-day-old rats [J].
Bona, E ;
Johansson, BB ;
Hagberg, H .
PEDIATRIC RESEARCH, 1997, 42 (05) :678-683
[5]   Regenerative Therapies in Neonatology: Clinical Perspectives [J].
Gortner, L. ;
Felderhoff-Mueser, U. ;
Monz, D. ;
Bieback, K. ;
Klueter, H. ;
Jellema, R. ;
Kramer, B. W. ;
Keller, M. ;
Reiss, I. ;
Horn, P. A. ;
Giebel, B. .
KLINISCHE PADIATRIE, 2012, 224 (04) :233-240
[6]   Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo [J].
Gronthos, S ;
Mankani, M ;
Brahim, J ;
Robey, PG ;
Shi, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :13625-13630
[7]   Putative Dental Pulp-Derived Stem/Stromal Cells Promote Proliferation and Differentiation of Endogenous Neural Cells in the Hippocampus of Mice [J].
Huang, Anderson Hsien-Cheng ;
Snyder, Brooke R. ;
Cheng, Pei-Hsun ;
Chan, Anthony W. S. .
STEM CELLS, 2008, 26 (10) :2654-2663
[8]   Multipotent mesenchymal stem cells with immunosuppressive activity can be easily isolated from dental pulp [J].
Pierdomenico, L ;
Bonsi, L ;
Calvitti, M ;
Rondelli, D ;
Arpinati, M ;
Chirumbolo, G ;
Becchetti, E ;
Marchionni, C ;
Alviano, F ;
Fossati, V ;
Staffolani, N ;
Franchina, M ;
Grossi, A ;
Bagnara, GP .
TRANSPLANTATION, 2005, 80 (06) :836-842
[9]   Cell Therapy for Neonatal Hypoxic-Ischemic Encephalopathy [J].
Pimentel-Coelho, Pedro M. ;
Mendez-Otero, Rosalia .
STEM CELLS AND DEVELOPMENT, 2010, 19 (03) :299-309
[10]   THE INFLUENCE OF IMMATURITY ON HYPOXIC-ISCHEMIC BRAIN-DAMAGE IN THE RAT [J].
RICE, JE ;
VANNUCCI, RC ;
BRIERLEY, JB .
ANNALS OF NEUROLOGY, 1981, 9 (02) :131-141