Combination of Stem Cell Mobilized by Granulocyte-Colony Stimulating Factor and Human Umbilical Cord Matrix Stem Cell: Therapy of Traumatic Brain Injury in Rats

被引:0
|
作者
Bakhtiary, Mehrdad [1 ,2 ]
Marzban, Mohsen [1 ,2 ]
Mehdizadeh, Mehdi [1 ,2 ]
Joghataei, Mohammad Taghi [1 ,2 ]
Khoei, Samideh [1 ,4 ]
Tondar, Mandi [2 ]
Mahabadi, Vahid Pirhajati [2 ]
Laribi, Bahareh [5 ]
Ebrahimi, Asghar [3 ]
Hashemian, Seyed Jafar [2 ]
Modiry, Navid [2 ]
Mehrabi, Soraya [6 ]
机构
[1] Univ Tehran Med Sci, Cellular & Mol Res Ctr, Tehran, Iran
[2] Univ Tehran Med Sci, Dept Anat, Tehran, Iran
[3] Milano Bicocca Univ, Dept Biosci & Biotechnol, Milan, Italy
[4] Univ Tehran Med Sci, Dept Med Phys, Tehran, Iran
[5] Univ Tehran Med Sci, Dept Immunol, Tehran, Iran
[6] Univ Tehran Med Sci, Dept Physiol, Tehran, Iran
关键词
Combine Therapy; G-CSF; Stem Cell; TBI; Wharton's jelly; MARROW STROMAL CELLS; FOCAL CEREBRAL-ISCHEMIA; BONE-MARROW; ADULT RATS; PERIPHERAL-BLOOD; FUNCTIONAL RECOVERY; TRANSPLANTATION; STROKE; PROLIFERATION; MODEL;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective(s) Clinical studies of treating traumatic brain injury (TBI) with autologous adult stem cells led us to examine the impression of a combination therapy. This was performed by intravenous injection of human umbilical cord matrix stem cell (hUCMSC-Wharton's jelly stem cell) with bone marrow cell mobilized by granulocytecolony stimulating factor (G-CSF) in rats injured with cortical compact device. Materials and Methods Adult male Wistar. rats (n= 50) were injured with controlled cortical impact device and divided into five groups. All injections were performed 1 day after injury into the tail veins of rats. Neurological functional evaluation of animals was performed before and after injury using modified neurological severity scores (mNSS). Animals were sacrificed 42 days after TBI and brain sections were stained by Brdu immunohistochemistry. Results Statistically significant improvement in functional outcome was observed in treatment groups when compared with control (P< 0.01). mNSS showed no significant differences among the hUCMSC and G-CSF treated groups at any time point (end of trial). Rats with hUCMSC + G-CSF treatment had a significant improvement on mNSS at 5 and 6 week compared to other treatment group (P< 0.01). Conclusion Histological analysis in G-CSF+ hUCMSC treated traumatic rats exhibited significant increase in numbers of Brdu immunoreactive cells in their traumatic core compared with other labeled group.
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收藏
页码:327 / 339
页数:13
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