中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2010年
10期
1009-1013
,共5页
唐国强%徐如祥%樊娟%姜晓丹%薛杉%酉建%蔡颖谦
唐國彊%徐如祥%樊娟%薑曉丹%薛杉%酉建%蔡穎謙
당국강%서여상%번연%강효단%설삼%유건%채영겸
胶原%支架%神经营养因子3%脊髓损伤
膠原%支架%神經營養因子3%脊髓損傷
효원%지가%신경영양인자3%척수손상
Collagen%Scaffold%Neurotrophin-3%Spinal cord injury
目的 研究天然有序胶原支架联合具有胶原靶向结合域(CBD)的神经营养因子3(NT3)(CBD-NT3)对背根节细胞(DRGs)突起延伸的影响,探讨这种联合策略对脊髓损伤修复的意义. 方法 将SD大鼠尾肌腱行去细胞处理制备胶原支架,HE染色评价支架的处理效果;去细胞处理后支架负载CBD-NT3并与SD大鼠原代DRGs体外共培养1、3、5 d,同时设NT3、PBS组作对照;FDA染色观察共培养后DRGs并定量分析各组细胞突起的长度及角度;扫描电镜观察共培养3 d后支架和DRGs的超微结构. 结果 HE染色显示经处理后支架内细胞成分基本去除;共培养3 d后CBD-NT3组DRGs突起延伸长度最长,与NT3组和PBS组比较差异均有统计学意义(P<0.05);细胞突起总体延伸方向与支架纤维长轴夹角的双侧95%可信区间为(18.8~20.7)°;扫描电镜显示DRGs能依靠胶原支架表面地貌锚定和生长. 结论 有序胶原支架联合CBD-NT3能定向引导并促进细胞突起延伸,为脊髓损伤修复的研究提供了一种有效的途径.
目的 研究天然有序膠原支架聯閤具有膠原靶嚮結閤域(CBD)的神經營養因子3(NT3)(CBD-NT3)對揹根節細胞(DRGs)突起延伸的影響,探討這種聯閤策略對脊髓損傷脩複的意義. 方法 將SD大鼠尾肌腱行去細胞處理製備膠原支架,HE染色評價支架的處理效果;去細胞處理後支架負載CBD-NT3併與SD大鼠原代DRGs體外共培養1、3、5 d,同時設NT3、PBS組作對照;FDA染色觀察共培養後DRGs併定量分析各組細胞突起的長度及角度;掃描電鏡觀察共培養3 d後支架和DRGs的超微結構. 結果 HE染色顯示經處理後支架內細胞成分基本去除;共培養3 d後CBD-NT3組DRGs突起延伸長度最長,與NT3組和PBS組比較差異均有統計學意義(P<0.05);細胞突起總體延伸方嚮與支架纖維長軸夾角的雙側95%可信區間為(18.8~20.7)°;掃描電鏡顯示DRGs能依靠膠原支架錶麵地貌錨定和生長. 結論 有序膠原支架聯閤CBD-NT3能定嚮引導併促進細胞突起延伸,為脊髓損傷脩複的研究提供瞭一種有效的途徑.
목적 연구천연유서효원지가연합구유효원파향결합역(CBD)적신경영양인자3(NT3)(CBD-NT3)대배근절세포(DRGs)돌기연신적영향,탐토저충연합책략대척수손상수복적의의. 방법 장SD대서미기건행거세포처리제비효원지가,HE염색평개지가적처리효과;거세포처리후지가부재CBD-NT3병여SD대서원대DRGs체외공배양1、3、5 d,동시설NT3、PBS조작대조;FDA염색관찰공배양후DRGs병정량분석각조세포돌기적장도급각도;소묘전경관찰공배양3 d후지가화DRGs적초미결구. 결과 HE염색현시경처리후지가내세포성분기본거제;공배양3 d후CBD-NT3조DRGs돌기연신장도최장,여NT3조화PBS조비교차이균유통계학의의(P<0.05);세포돌기총체연신방향여지가섬유장축협각적쌍측95%가신구간위(18.8~20.7)°;소묘전경현시DRGs능의고효원지가표면지모묘정화생장. 결론 유서효원지가연합CBD-NT3능정향인도병촉진세포돌기연신,위척수손상수복적연구제공료일충유효적도경.
Objective To investigate the effect of collagen scaffold loaded with collagen-binding domain neurotrophin-3 (CBD-NT3) on the extension of cellular processes of dorsal root ganglions (DRGs), and explore the significance of this kind of combinatorial strategies in the spinal cord injury repair. Methods The tail tendons of SD neonatal rats were performed the removal of cellular components to prepare the collagen scaffold; HE staining was employed to evaluate whether the cells were completely removed from the collagen scaffold. The collagen scaffold was loaded with CBD-NT3,and then, they were co-cultured with primary DRGs for 1, 3 and 5 d, respectively. NT3 and PBS were also co-cultured with primary DRGs for 1, 3 and 5 d, respectively, as controls. Cells on the scaffold were stained by fluorescein diacetate (FDA) for morphology observation and the lengths and angles of the processes in each group were also quantitatively analyzed. Scanning electron microcopy (SEM) was employed to observe the topography of scaffold and the ultrastructure of DRGs 3 d after the co-culture.Results HE staining indicated that the cellular components in the scaffold were removed completely.The length of processes elongation in CBD-NT3 treatment group was significantly longer than that in the controls 3 d after the co-culture (P<0.05). The 95% confidence interval of the angle between the line which the process emerged from the cell soma to the growing tip of the process and the long axis of fiber was 18.8-20.7 degrees. The results of SEM showed that cells could rely on the topography of the scaffold to anchor and grow. Conclusion The combinatorial strategies of collagen scaffold with CBD-NT3 can play a double function for oriented guiding and inducing extension of cellular processes effectively,which may provide a better therapeutic approach for spinal cord injury repair.