中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
49期
7903-7907
,共5页
赵斌%陈宝%赵海燕%王栓科
趙斌%陳寶%趙海燕%王栓科
조빈%진보%조해연%왕전과
实验动物%组织工程%音猬因子%脊髓损伤%急性压迫%神经再生
實驗動物%組織工程%音猬因子%脊髓損傷%急性壓迫%神經再生
실험동물%조직공정%음위인자%척수손상%급성압박%신경재생
hedgehogs%ligands%spinal cord injuries%nerve regeneration
背景:在神经系统的发育中,音猬因子信号通路的主要作用为诱导整个中枢神经系统形成背腹两侧分区,当这一信号通路受到破坏时,将导致整个中枢神经系统腹侧表型神经元的完全丧失。目的:制造成年大鼠急性压迫性脊髓损伤模型,检测脊髓急性压迫性损伤后与发育相关的重要分子音猬因子的表达,探讨其在神经再生过程中所发挥的作用。方法:将30只同龄SD大鼠置入后路压迫装置,制作成急性压迫性脊髓损伤模型。随机分为椎板钻孔组5只和急性脊髓损伤组25只。应用原位杂交检测方法,分别于脊髓损伤后1,3,5,7,14 d对损伤区行音猬因子mRNA检测。结果与结论:脊髓损伤后7 d,音猬因子表达水平达到最大值,在损伤区至远端10 mm处的灰质和白质中都有表达。音猬因子在室管膜细胞的表达明显低于在灰质和白质中的表达;其在室管膜区域的表达仅限于损伤区域周围5 mm的范围内,分布范围明显小于在灰质和白质中的表达。提示激活急性压迫性脊髓损伤模型音猬因子的表达,可能和损伤脊髓神经的再生有关。
揹景:在神經繫統的髮育中,音猬因子信號通路的主要作用為誘導整箇中樞神經繫統形成揹腹兩側分區,噹這一信號通路受到破壞時,將導緻整箇中樞神經繫統腹側錶型神經元的完全喪失。目的:製造成年大鼠急性壓迫性脊髓損傷模型,檢測脊髓急性壓迫性損傷後與髮育相關的重要分子音猬因子的錶達,探討其在神經再生過程中所髮揮的作用。方法:將30隻同齡SD大鼠置入後路壓迫裝置,製作成急性壓迫性脊髓損傷模型。隨機分為椎闆鑽孔組5隻和急性脊髓損傷組25隻。應用原位雜交檢測方法,分彆于脊髓損傷後1,3,5,7,14 d對損傷區行音猬因子mRNA檢測。結果與結論:脊髓損傷後7 d,音猬因子錶達水平達到最大值,在損傷區至遠耑10 mm處的灰質和白質中都有錶達。音猬因子在室管膜細胞的錶達明顯低于在灰質和白質中的錶達;其在室管膜區域的錶達僅限于損傷區域週圍5 mm的範圍內,分佈範圍明顯小于在灰質和白質中的錶達。提示激活急性壓迫性脊髓損傷模型音猬因子的錶達,可能和損傷脊髓神經的再生有關。
배경:재신경계통적발육중,음위인자신호통로적주요작용위유도정개중추신경계통형성배복량측분구,당저일신호통로수도파배시,장도치정개중추신경계통복측표형신경원적완전상실。목적:제조성년대서급성압박성척수손상모형,검측척수급성압박성손상후여발육상관적중요분자음위인자적표체,탐토기재신경재생과정중소발휘적작용。방법:장30지동령SD대서치입후로압박장치,제작성급성압박성척수손상모형。수궤분위추판찬공조5지화급성척수손상조25지。응용원위잡교검측방법,분별우척수손상후1,3,5,7,14 d대손상구행음위인자mRNA검측。결과여결론:척수손상후7 d,음위인자표체수평체도최대치,재손상구지원단10 mm처적회질화백질중도유표체。음위인자재실관막세포적표체명현저우재회질화백질중적표체;기재실관막구역적표체부한우손상구역주위5 mm적범위내,분포범위명현소우재회질화백질중적표체。제시격활급성압박성척수손상모형음위인자적표체,가능화손상척수신경적재생유관。
BACKGROUND:In the development of nervous system, the main effect of sonic hedgehog signaling pathway is to induce the partition of dorsal and ventral sides in the central nervous system. When above signaling pathway is destroyed, ventral neurons in the central nervous system wil completely lose. OBJECTIVE: To establish adult rat models of acute compressive spinal cord injury, to detect the expression of development-related sonic hedgehog after acute compressive spinal cord injury, and to explore its effects on neural regeneration. METHODS:A total of 30 Sprague-Dawley rats at the same age were placed in a posterior compression device to establish models of acute compressive spinal cord injury. They were then randomly divided into lamina driling group (n=5) and acute spinal cord injury group (n=25). Sonic hedgehog mRNA was detected by in situ hybridization method at the injury site at 1, 3, 5, 7, and 14 days after spinal cord. RESULTS AND CONCLUSION:The expression levels of sonic hedgehog increased to the maximal expression levels in grey and white matters 10 mm distal to the lesion site at 7 days after injury. Sonic hedgehog expression was apparently less in ependymal cels than in grey and white matters and was restricted to 5 mm distal to the lesion site, being narrower in its distribution than its occurrence in grey and white matters. These data indicated that acute compressive spinal cord injury can induce the expression of sonic hedgehog. This expression maybe relates to adult neural cel regeneration.