中国组织工程研究与临床康复
中國組織工程研究與臨床康複
중국조직공정연구여림상강복
JOURNAL OF CLINICAL REHABILITATIVE TISSUE ENGINEERING RESEARCH
2010年
6期
1053-1057
,共5页
王国毓%贺西京%袁普卫%李浩鹏%常瑞
王國毓%賀西京%袁普衛%李浩鵬%常瑞
왕국육%하서경%원보위%리호붕%상서
嗅鞘细胞%移植%脊髓损伤%形态学%病理学%大鼠
嗅鞘細胞%移植%脊髓損傷%形態學%病理學%大鼠
후초세포%이식%척수손상%형태학%병이학%대서
背景:对于脊髓损伤,目前临床尚无有效的治疗对策,近年来嗅鞘细胞移植对脊髓损伤修复取得了一定的进展.目的:观察嗅鞘细胞移植在缓解损伤脊髓的病理反应和超微结构变化,及其在发生发展中的作用.方法:60只大鼠随机分为空白组,模型组,嗅鞘胞移植组和DF12组,每组15只.空白组:仅切开T_(10)全椎板及T_9,T_(11)部分椎板,对脊髓未作其他处理,明胶海绵轻柔压迫止血;模型组:仅切断脊髓,未作特殊处理;嗅鞘细胞移植组和DF12组:切断脊髓后用微量注射器分别注射嗅鞘细胞和DF12培养液,随后缝合切口.脊髓损伤后1,3,7,14,28,42,56 d每组麻醉2只受检大鼠,取材做光镜观察和电镜观察.结果与结论:单纯脊髓横切损伤后,发生了出血、水肿、变性、坏死以及囊腔形成,胶质细胞增生和神经纤维再生.嗅鞘细胞移植后,明显减轻了神经元和神经纤维的坏死变性程度,减轻病理反应,并能对损伤神经元实施保护;防止了胶质细胞过度增生形成瘢痕屏障,明显增加了再生神经纤维的数量.提示嗅鞘细胞移植对损伤脊髓具有减轻病理反应和促进修复的作用.
揹景:對于脊髓損傷,目前臨床尚無有效的治療對策,近年來嗅鞘細胞移植對脊髓損傷脩複取得瞭一定的進展.目的:觀察嗅鞘細胞移植在緩解損傷脊髓的病理反應和超微結構變化,及其在髮生髮展中的作用.方法:60隻大鼠隨機分為空白組,模型組,嗅鞘胞移植組和DF12組,每組15隻.空白組:僅切開T_(10)全椎闆及T_9,T_(11)部分椎闆,對脊髓未作其他處理,明膠海綿輕柔壓迫止血;模型組:僅切斷脊髓,未作特殊處理;嗅鞘細胞移植組和DF12組:切斷脊髓後用微量註射器分彆註射嗅鞘細胞和DF12培養液,隨後縫閤切口.脊髓損傷後1,3,7,14,28,42,56 d每組痳醉2隻受檢大鼠,取材做光鏡觀察和電鏡觀察.結果與結論:單純脊髓橫切損傷後,髮生瞭齣血、水腫、變性、壞死以及囊腔形成,膠質細胞增生和神經纖維再生.嗅鞘細胞移植後,明顯減輕瞭神經元和神經纖維的壞死變性程度,減輕病理反應,併能對損傷神經元實施保護;防止瞭膠質細胞過度增生形成瘢痕屏障,明顯增加瞭再生神經纖維的數量.提示嗅鞘細胞移植對損傷脊髓具有減輕病理反應和促進脩複的作用.
배경:대우척수손상,목전림상상무유효적치료대책,근년래후초세포이식대척수손상수복취득료일정적진전.목적:관찰후초세포이식재완해손상척수적병리반응화초미결구변화,급기재발생발전중적작용.방법:60지대서수궤분위공백조,모형조,후초포이식조화DF12조,매조15지.공백조:부절개T_(10)전추판급T_9,T_(11)부분추판,대척수미작기타처리,명효해면경유압박지혈;모형조:부절단척수,미작특수처리;후초세포이식조화DF12조:절단척수후용미량주사기분별주사후초세포화DF12배양액,수후봉합절구.척수손상후1,3,7,14,28,42,56 d매조마취2지수검대서,취재주광경관찰화전경관찰.결과여결론:단순척수횡절손상후,발생료출혈、수종、변성、배사이급낭강형성,효질세포증생화신경섬유재생.후초세포이식후,명현감경료신경원화신경섬유적배사변성정도,감경병리반응,병능대손상신경원실시보호;방지료효질세포과도증생형성반흔병장,명현증가료재생신경섬유적수량.제시후초세포이식대손상척수구유감경병리반응화촉진수복적작용.
BACKGROUND: There are no effective treatments for spinal cord injury. Transplantation of olfactory ensheathing cells (OECs) has achieved great progress in repairing spinal cord injury. OBJECTIVE: To observe the effect of OECs transplantation on pathological and ultrastructural alterations of spinal cord, and the role in spinal cord injury developing.METHODS: A total of 60 SD rats were randomly divided into blank, model, transplantation and DF12 groups, with 15 animals in each group. The entire vertebral plate of T_(10), and partial vertebral plate of T_9 and T_(11) of blank group were cut open, and gelatin sponge was used for hemostasis. In the model group, the spinal cord was excised. In the transplantation and DF12 groups, OECs and DF12 culture solution were injected following spinal cord excision. The incision was sutured. Two rats from each group were anesthetized 1, 3, 7, 14, 28, 42, and 56 days following injury, and injured areas were observed by light microscopy and electron microscopy. RESULTS AND CONCLUSION: Following spinal cord injury, pathological and ultrastructural changes occurred, such as hemorrhage, edema, degeneration, necrosis, cavitation, gliacyte proliferation and nerve fiber regeneration. OECs transplantation attenuated neuronal and nerve fiber necrosis, relieved degree of pathological reaction, protected injured neurons, prevented gliacyte proliferation and increased nerve fiber regeneration. Results show that OECs transplantation ameliorated pathological reactions and promoted spinal cord injury repair.