Therapeutic Effect of BDNF-Overexpressing Human Neural Stem Cells (F3.BDNF) in a Contusion Model of Spinal Cord Injury in Rats

被引:25
作者
Chang, Da-Jeong [1 ]
Cho, Hwi-Young [2 ]
Hwang, Seyoung [1 ]
Lee, Nayeon [1 ]
Choi, Chunggab [1 ]
Lee, Hyunseung [3 ]
Hong, Kwan Soo [3 ]
Oh, Seung-Hun [4 ]
Kim, Hyun Sook [4 ]
Shin, Dong Ah [5 ]
Yoon, Young Wook [6 ]
Song, Jihwan [1 ,7 ]
机构
[1] CHA Univ, CHA Stem Cell Inst, Dept Biomed Sci, 335 Pangyo Ro, Seongnam Si 13488, Gyeonggi Do, South Korea
[2] Gachon Univ, Dept Phys Therapy, 191 Hambakmoero, Incheon 21936, South Korea
[3] Korea Basic Sci Inst, Res Ctr Bioconvergence Anal, 162 Yeongudanji Ro, Cheongju 28119, Chungcheongbuk, South Korea
[4] CHA Univ, CHA Bundang Med Ctr, Dept Neurol, 59 Yatap Ro, Seongnam Si 13496, Gyeonggi Do, South Korea
[5] Yonsei Univ, Coll Med, Dept Neurosurg, 50-1 Yonsei Ro, Seoul 03722, South Korea
[6] Korea Univ, Coll Med, Dept Physiol, Anam Dong 5 Ga, Seoul 02841, South Korea
[7] iPS Bio Inc, 3F,16 Daewangpangyo Ro 712 Beon Gil, Seongnam Si 13488, Gyeonggi Do, South Korea
关键词
spinal cord injury; contusion; neural stem cells; brain-derived neurotrophic factor (BDNF); functional recovery; PROMOTE FUNCTIONAL RECOVERY; AXONAL REGENERATION; LOCOMOTOR RECOVERY; TRANSPLANTATION; NEUROPROTECTION; PAIN; IMMUNOMODULATION; DIFFERENTIATION; REMYELINATION; ACTIVATION;
D O I
10.3390/ijms22136970
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The most common type of spinal cord injury is the contusion of the spinal cord, which causes progressive secondary tissue degeneration. In this study, we applied genetically modified human neural stem cells overexpressing BDNF (brain-derived neurotrophic factor) (F3.BDNF) to determine whether they can promote functional recovery in the spinal cord injury (SCI) model in rats. We transplanted F3.BDNF cells via intrathecal catheter delivery after a contusion of the thoracic spinal cord and found that they were migrated toward the injured spinal cord area by MR imaging. Transplanted F3.BDNF cells expressed neural lineage markers, such as NeuN, MBP, and GFAP and were functionally connected to the host neurons. The F3.BDNF-transplanted rats exhibited significantly improved locomotor functions compared with the sham group. This functional recovery was accompanied by an increased volume of spared myelination and decreased area of cystic cavity in the F3.BDNF group. We also observed that the F3.BDNF-transplanted rats showed reduced numbers of Iba1- and iNOS-positive inflammatory cells as well as GFAP-positive astrocytes. These results strongly suggest the transplantation of F3.BDNF cells can modulate inflammatory cells and glia activation and also improve the hyperalgesia following SCI.
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页数:17
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