AIM: To determine the tissue and temporal distribution of human umbilical cord matrix stem (hUCMS) cells in severe combined immunodeficiency (SCID) mice. METHODS: For studying the localization of hUCMS cells, tritiate...AIM: To determine the tissue and temporal distribution of human umbilical cord matrix stem (hUCMS) cells in severe combined immunodeficiency (SCID) mice. METHODS: For studying the localization of hUCMS cells, tritiated thymidine-labeled hUCMS cells were injected in SCID mice and tissue distribution was quantitatively determined using a liquid scintillation counter at days 1, 3, 7 and 14. Furthermore, an immunofluorescence detection technique was employed in which anti-human mitochondrial antibody was used to identify hUCMS cells in mouse tissues. In order to visualize the distribution of transplanted hUCMS cells in H&E stained tissue sections, India Black ink 4415 was used to label the hUCMS cells. RESULTS: When tritiated thymidine-labeled hUCMS cells were injected systemically (iv) in female SCID mice, the lung was the major site of accumulation at 24 h after transplantation. With time, the cells migrated to other tissues, and on day three, the spleen, stomach, and small and large intestines were the major accumulation sites. On day seven, a relatively large amount of radioactivity was detected in the adrenal gland, uterus, spleen, lung, and digestive tract. In addition, labeled cells had crossed the blood brain barrier by day 1. CONCLUSION: These results indicate that peripherally injected hUCMS cells distribute quantitatively in a tissue-specific manner throughout the body.展开更多
Acellular peripheral allograft scaffolds can be fabricated using chemical extraction techniques,but methods for producing acellular scaffold derived from spinal cord tissue are not currently available.The present stud...Acellular peripheral allograft scaffolds can be fabricated using chemical extraction techniques,but methods for producing acellular scaffold derived from spinal cord tissue are not currently available.The present study demonstrated that chemical extraction using Triton X-100 and sodium deoxycholate could be used to completely remove the cells,axons and neural sheaths in spinal cord extracellular matrix-derived scaffolds.The matrix fibers were longitudinally arranged in a wave-like formation,and were connected by fiber junctions.Lattice-shaped fiber cages appeared and developed into bone trabecula-like changes.The natural structure of matrix fibers in the scaffolds was maintained;this helps to guide the differentiation and migration of implanted stem cells.Decellularized spinal cord extracellular matrix-derived scaffolds can provide an ideal substance for fabricating tissue-engineered spinal cord.展开更多
Alternatively activated macrophages （M2 macrophages） promote central nervous system regeneration. Our previous study demonstrated that treatment with peripheral nerve grafts and fibroblast growth factor-1 recruited ...Alternatively activated macrophages （M2 macrophages） promote central nervous system regeneration. Our previous study demonstrated that treatment with peripheral nerve grafts and fibroblast growth factor-1 recruited more M2 macrophages and improved partial functional recovery in spinal cord transected rats. The migration of macrophages is matrix metalloproteinase （MMP） dependent. We used a general inhibitor of MMPs to influence macrophage migration, and we examined the migration of macrophage populations and changes in spinal function. Rat spinal cords were completely transected at Ts, and 5 mm of spinal cord was removed （group T）. In group R, spinal cord-transected rats received treatment with fibroblast grow th factor- 1 and peripheral nerve grafts. In group RG, rats received the same treatment as group R with the addition of 200 μM GM6001 （an MMP inhibitor） to the fibrin mix. We found that MMP-9, but not MMP- 2, was upregulated in the graft area of rats in group R. Local application of the MMP inhibitor resulted in a reduction in the ratio of arginase-1 （M2 macrophage subset）/inducible nitric oxide synthase-postive cells. When the MMP inhibitor was applied at 8 weeks postoperation, the partial functional recovery observed in group R was lost. This effect was accompanied by a decrease in brain-derived neurotrophic factor levels in the nerve graft. These results suggested that the arginase-1 positive population in spinal cord transected rats is a migratory cell population rather than the phenotypic conversion of early iNOS^＋ cells and that the migration of the arginase-1^＋ population could be regulated locally. Simultaneous application of MMP in- hibitors or promotion of MMP activity for spinal cord injury needs to be considered if the coadministered treatment involves M2 recruitment.展开更多
In cell therapy protocols, many tissues were proposed as a source of mesenchymal stem cells(MSC) isolation. So far, bone marrow(BM) has been presented as the main source of MSC despite the invasive isolation pro-cedur...In cell therapy protocols, many tissues were proposed as a source of mesenchymal stem cells(MSC) isolation. So far, bone marrow(BM) has been presented as the main source of MSC despite the invasive isolation pro-cedure related to this source. During the last years, the umbilical cord(UC) matrix was cited in different studies as a reliable source from which long term ex vivo prolif-erating fibroblasts were isolated but with contradictory data about their immunophenotype, gene expression profile, and differentiation potential. Hence, an inter-esting question emerged: Are cells isolated from cord matrix(UC-MSC) different from other MSCs? In this re-view, we will summarize different studies that isolated and characterized UC-MSC. Considering BM-MSC as gold standard, we will discuss if UC-MSC fulfill different criteria that define MSC, and what remain to be done in this issue.展开更多
Propofol has been shown to exert neuroprotective effects on the injured spinal cord.However,the effect of propofol on the blood-spinal cord barrier（BSCB） after ischemia/reperfusion injury（IRI） is poorly understood...Propofol has been shown to exert neuroprotective effects on the injured spinal cord.However,the effect of propofol on the blood-spinal cord barrier（BSCB） after ischemia/reperfusion injury（IRI） is poorly understood.Therefore,we investigated whether propofol could maintain the integrity of the BSCB.Spinal cord IRI（SCIRI） was induced in rabbits by infrarenal aortic occlusion for 30 minutes.Propofol,30 mg/kg,was intravenously infused 10 minutes before aortic clamping as well as at the onset of reperfusion.Then,48 hours later,we performed histological and m RNA/protein analyses of the spinal cord.Propofol decreased histological damage to the spinal cord,attenuated the reduction in BSCB permeability,downregulated the m RNA and protein expression levels of matrix metalloprotease-9（MMP-9） and nuclear factor-κB（NF-κB）,and upregulated the protein expression levels of occludin and claudin-5.Our findings suggest that propofol helps maintain BSCB integrity after SCIRI by reducing MMP-9 expression,by inhibiting the NF-κB signaling pathway,and by maintaining expression of tight junction proteins.展开更多
We derive explicit expressions for quantum discord and classical correlation for an X structure density matrix. Based on the characteristics of the expressions, the quantum discord and the classical correlation are ea...We derive explicit expressions for quantum discord and classical correlation for an X structure density matrix. Based on the characteristics of the expressions, the quantum discord and the classical correlation are easily obtained and compared under different initial conditions using a novel analytical method. We explain the relationships among quantum discord, classical correlation, and entanglement, and further find that the quantum discord is not always larger than the entanglement measured by concurrence in a general two-qubit X state. The new method, which is different from previous approaches, has certain guiding significance for analysing quantum discord and classical correlation of a two-qubit X state, such as a mixed state.展开更多
目的 本研究旨在探讨细胞外基质刚度变化对神经干细胞(neural stem cells,NSCs)分化的影响及其作用机制。方法 本研究基于成功构建脊髓损伤大鼠模型,并制备不同刚度(0.7 k Pa、40 k Pa)的聚丙烯酰胺凝胶基底,将大鼠原代NSCs于不同刚度...目的 本研究旨在探讨细胞外基质刚度变化对神经干细胞(neural stem cells,NSCs)分化的影响及其作用机制。方法 本研究基于成功构建脊髓损伤大鼠模型,并制备不同刚度(0.7 k Pa、40 k Pa)的聚丙烯酰胺凝胶基底,将大鼠原代NSCs于不同刚度基底上培养。压电型机械敏感离子通道组件1 (piezo type mechanosensitive ion channel component 1,Piezo1) sh RNA质粒转染NSCs细胞。免疫荧光染色检测神经元标志物双皮质醇(doublecortion,DCX)和星形胶质细胞标志物胶质纤维酸性蛋白(glial fibrillary acidic protein,GFAP)阳性细胞百分比。免疫组织化学及蛋白质免疫印迹(Western blot)法检测损伤组织及NSCs细胞中Piezo1蛋白的表达水平。结果 与0.7 k Pa基质刚度组相比,40 k Pa基质刚度组中DCX阳性细胞数增加,而GFAP阳性细胞数减少,Piezo1蛋白表达量上升。脊髓损伤大鼠损伤组织Piezo1蛋白表达显著高于空白对照(sham)组。40 k Pa基质刚度条件下沉默Piezo1后,DCX阳性细胞数减少,而GFAP阳性细胞数增加,差异具有统计学意义(P<0.05)。机制研究发现,沉默Piezo1导致IV型胶原及纤连蛋白表达下降。重组纤连蛋白逆转了Piezo1 sh RNA对NSCs分化的影响,即DCX阳性细胞数增加,而GFAP阳性细胞数减少。结论 综上可见,硬基底刚度通过促进Piezo1蛋白表达,上调IV型胶原及纤连蛋白表达,从而调控NSCs细胞分化。本研究为基于生物材料治疗脊髓损伤提供了新的视角。展开更多
The scarring response after a penetrant central nervous system injury results from the interaction between invading leptominingeal/pericyte-derived fibroblasts and endogenous reactive astrocytes about the wound margin...The scarring response after a penetrant central nervous system injury results from the interaction between invading leptominingeal/pericyte-derived fibroblasts and endogenous reactive astrocytes about the wound margin. Extracellular matrix and scar-derived axon growth inhibitory mole- cules fill the lesion site providing both a physical and chemical barrier to regenerating axons. Dec orin, a small leucine-rich chondroitin-dermatan sulphate proteoglycan expressed by neurons and astrocytes in the central nervous system, is both anti-fibrotic and anti-inflammatory and attenu- ates the formation and partial dissolution of established and chronic scars. Here, we discuss the potential of using Decorin to antagonise scarring in the central nervous system.展开更多
目的:探讨损伤控制手术(damage control operation)治疗兔脊髓压迫性损伤的效果。方法:应用球囊压迫法制备新西兰大白兔脊髓压迫损伤模型45只,造模术后2d随机取5只完成行为学观测、评分后取出损伤区脊髓组织进行流式细胞仪凋亡细胞检测...目的:探讨损伤控制手术(damage control operation)治疗兔脊髓压迫性损伤的效果。方法:应用球囊压迫法制备新西兰大白兔脊髓压迫损伤模型45只,造模术后2d随机取5只完成行为学观测、评分后取出损伤区脊髓组织进行流式细胞仪凋亡细胞检测、病理学观察、免疫组化染色检测兔损伤区脊髓组织中基质金属蛋白酶2(MMP-2)表达(对照组),剩余40只随机分为两组,每组20只,一组采用损伤控制手术(A组),即减压术前先将球囊内压力减为原来一半,使椎管内有效容积增加后再自远离脊髓压迫较重的一侧进行全椎板减压;另一组直接予全椎板切除减压,减压自压迫最严重部位开始(B组),两组减压完毕后均取出球囊,并在减压术后1d、3d、7d、14d分别随机取5只实验兔完成以上检测内容。结果:对照组造模术后48h的Tarlov评分为1.20±0.45分,A、B组减压术后1d时Tarlov评分与对照组比较均无统计学差异(P>0.05);A、B组减压术后1d、3d、7d时的Tarlov评分均无统计学差异(P>0.05),减压术后14d时A组高于B组(P<0.05)。对照组脊髓细胞凋亡率为(2.66±1.40)%,A、B组减压术后1d时脊髓细胞凋亡率均低于对照组(P<0.05);减压术后1d、3d时A、B两组损伤区脊髓细胞凋亡率无统计学差异(P>0.05);A、B组减压术后1d与3d、7d与14d损伤区脊髓细胞凋亡率无统计学差异(P>0.05);A、B组减压术后3d与7d损伤区脊髓细胞凋亡率均有统计学差异(P<0.05);减压术后7d、14d时A组损伤区脊髓细胞凋亡率均低于同时间点B组(P<0.05)。病理学观察显示对照组白质轻度脱髓鞘、部分轴突空泡样变,灰质内细胞水肿,A、B组减压术后1d、3d、7d、14d白质弥漫性脱髓鞘改变及散在点状出血,灰质内细胞水肿伴神经细胞变性逐渐加重,至减压术后7d时灰质内广泛神经细胞变性,并持续到术后14d。对照组MMP-2表达阳性细胞率为(45.76±0.75)%,A、B组减压术后1d时MMP-2表达阳性率均低于对照组(P<0.05);减压术后1d、3d、7d、14d时B组MMP-2表达阳性细胞率均高于同时间点A组(P<0.05),A、B组减压术后1d、3d比较均无统计学差异(P>0.05),3d、7d,7d、14d比较均有统计学差异(P<0.05)。结论:损伤控制手术治疗兔脊髓压迫性损伤较直接减压效果好,建议对胸腰椎爆裂骨折合并脊髓压迫损伤的治疗采用损伤控制手术方案。展开更多
基金Supported by (in part) the Kansas State University (KSU) Terry C. Johnson Center for Basic Cancer Researchthe KSU College of Veterinary Medicine Dean's FundKSU Targeted Excellence, Kansas State Legislative Appropriation and NIH1R21CA135599
文摘AIM: To determine the tissue and temporal distribution of human umbilical cord matrix stem (hUCMS) cells in severe combined immunodeficiency (SCID) mice. METHODS: For studying the localization of hUCMS cells, tritiated thymidine-labeled hUCMS cells were injected in SCID mice and tissue distribution was quantitatively determined using a liquid scintillation counter at days 1, 3, 7 and 14. Furthermore, an immunofluorescence detection technique was employed in which anti-human mitochondrial antibody was used to identify hUCMS cells in mouse tissues. In order to visualize the distribution of transplanted hUCMS cells in H&E stained tissue sections, India Black ink 4415 was used to label the hUCMS cells. RESULTS: When tritiated thymidine-labeled hUCMS cells were injected systemically (iv) in female SCID mice, the lung was the major site of accumulation at 24 h after transplantation. With time, the cells migrated to other tissues, and on day three, the spleen, stomach, and small and large intestines were the major accumulation sites. On day seven, a relatively large amount of radioactivity was detected in the adrenal gland, uterus, spleen, lung, and digestive tract. In addition, labeled cells had crossed the blood brain barrier by day 1. CONCLUSION: These results indicate that peripherally injected hUCMS cells distribute quantitatively in a tissue-specific manner throughout the body.
基金Science Foundation of Shaoguan in Guangdong Province, No. 2010-07the Natural Science Foundation of Guangdong Province, China, No. 10451202602005995
文摘Acellular peripheral allograft scaffolds can be fabricated using chemical extraction techniques,but methods for producing acellular scaffold derived from spinal cord tissue are not currently available.The present study demonstrated that chemical extraction using Triton X-100 and sodium deoxycholate could be used to completely remove the cells,axons and neural sheaths in spinal cord extracellular matrix-derived scaffolds.The matrix fibers were longitudinally arranged in a wave-like formation,and were connected by fiber junctions.Lattice-shaped fiber cages appeared and developed into bone trabecula-like changes.The natural structure of matrix fibers in the scaffolds was maintained;this helps to guide the differentiation and migration of implanted stem cells.Decellularized spinal cord extracellular matrix-derived scaffolds can provide an ideal substance for fabricating tissue-engineered spinal cord.
基金supported by the National Science Council(102-2320-B-324-001),Chinaupported by grants from Taipei Veterans General Hospital(V103E6-001&V104E6-001)by grants(MOST 104-2314-B-010-012-MY3,MOST 105-2314-B-010-013-MY2 and MOST 106-2632-B-324-001)from the Ministry of Science and Technology in Taiwan,China
文摘Alternatively activated macrophages （M2 macrophages） promote central nervous system regeneration. Our previous study demonstrated that treatment with peripheral nerve grafts and fibroblast growth factor-1 recruited more M2 macrophages and improved partial functional recovery in spinal cord transected rats. The migration of macrophages is matrix metalloproteinase （MMP） dependent. We used a general inhibitor of MMPs to influence macrophage migration, and we examined the migration of macrophage populations and changes in spinal function. Rat spinal cords were completely transected at Ts, and 5 mm of spinal cord was removed （group T）. In group R, spinal cord-transected rats received treatment with fibroblast grow th factor- 1 and peripheral nerve grafts. In group RG, rats received the same treatment as group R with the addition of 200 μM GM6001 （an MMP inhibitor） to the fibrin mix. We found that MMP-9, but not MMP- 2, was upregulated in the graft area of rats in group R. Local application of the MMP inhibitor resulted in a reduction in the ratio of arginase-1 （M2 macrophage subset）/inducible nitric oxide synthase-postive cells. When the MMP inhibitor was applied at 8 weeks postoperation, the partial functional recovery observed in group R was lost. This effect was accompanied by a decrease in brain-derived neurotrophic factor levels in the nerve graft. These results suggested that the arginase-1 positive population in spinal cord transected rats is a migratory cell population rather than the phenotypic conversion of early iNOS^＋ cells and that the migration of the arginase-1^＋ population could be regulated locally. Simultaneous application of MMP in- hibitors or promotion of MMP activity for spinal cord injury needs to be considered if the coadministered treatment involves M2 recruitment.
文摘In cell therapy protocols, many tissues were proposed as a source of mesenchymal stem cells(MSC) isolation. So far, bone marrow(BM) has been presented as the main source of MSC despite the invasive isolation pro-cedure related to this source. During the last years, the umbilical cord(UC) matrix was cited in different studies as a reliable source from which long term ex vivo prolif-erating fibroblasts were isolated but with contradictory data about their immunophenotype, gene expression profile, and differentiation potential. Hence, an inter-esting question emerged: Are cells isolated from cord matrix(UC-MSC) different from other MSCs? In this re-view, we will summarize different studies that isolated and characterized UC-MSC. Considering BM-MSC as gold standard, we will discuss if UC-MSC fulfill different criteria that define MSC, and what remain to be done in this issue.
基金supported by the Natural Science Foundation of Hubei Province of China,No.2013CFB086the Basic Research Funds of the Huazhong University of Science & Technology of China,No.2016YXZDO24the Scientific Research Project of the Health and Family Planning Commission of Hubei Province of China,No.WJ2015MB023
文摘Propofol has been shown to exert neuroprotective effects on the injured spinal cord.However,the effect of propofol on the blood-spinal cord barrier（BSCB） after ischemia/reperfusion injury（IRI） is poorly understood.Therefore,we investigated whether propofol could maintain the integrity of the BSCB.Spinal cord IRI（SCIRI） was induced in rabbits by infrarenal aortic occlusion for 30 minutes.Propofol,30 mg/kg,was intravenously infused 10 minutes before aortic clamping as well as at the onset of reperfusion.Then,48 hours later,we performed histological and m RNA/protein analyses of the spinal cord.Propofol decreased histological damage to the spinal cord,attenuated the reduction in BSCB permeability,downregulated the m RNA and protein expression levels of matrix metalloprotease-9（MMP-9） and nuclear factor-κB（NF-κB）,and upregulated the protein expression levels of occludin and claudin-5.Our findings suggest that propofol helps maintain BSCB integrity after SCIRI by reducing MMP-9 expression,by inhibiting the NF-κB signaling pathway,and by maintaining expression of tight junction proteins.
基金supported by the Natural Science Foundation of Hunan Province of China (Grant No. 09JJ6011)the Natural Science Foundation of Education Department of Hunan Province, China (Grant Nos. 08A055 and 07C528)
文摘We derive explicit expressions for quantum discord and classical correlation for an X structure density matrix. Based on the characteristics of the expressions, the quantum discord and the classical correlation are easily obtained and compared under different initial conditions using a novel analytical method. We explain the relationships among quantum discord, classical correlation, and entanglement, and further find that the quantum discord is not always larger than the entanglement measured by concurrence in a general two-qubit X state. The new method, which is different from previous approaches, has certain guiding significance for analysing quantum discord and classical correlation of a two-qubit X state, such as a mixed state.
文摘目的 本研究旨在探讨细胞外基质刚度变化对神经干细胞(neural stem cells,NSCs)分化的影响及其作用机制。方法 本研究基于成功构建脊髓损伤大鼠模型,并制备不同刚度(0.7 k Pa、40 k Pa)的聚丙烯酰胺凝胶基底,将大鼠原代NSCs于不同刚度基底上培养。压电型机械敏感离子通道组件1 (piezo type mechanosensitive ion channel component 1,Piezo1) sh RNA质粒转染NSCs细胞。免疫荧光染色检测神经元标志物双皮质醇(doublecortion,DCX)和星形胶质细胞标志物胶质纤维酸性蛋白(glial fibrillary acidic protein,GFAP)阳性细胞百分比。免疫组织化学及蛋白质免疫印迹(Western blot)法检测损伤组织及NSCs细胞中Piezo1蛋白的表达水平。结果 与0.7 k Pa基质刚度组相比,40 k Pa基质刚度组中DCX阳性细胞数增加,而GFAP阳性细胞数减少,Piezo1蛋白表达量上升。脊髓损伤大鼠损伤组织Piezo1蛋白表达显著高于空白对照(sham)组。40 k Pa基质刚度条件下沉默Piezo1后,DCX阳性细胞数减少,而GFAP阳性细胞数增加,差异具有统计学意义(P<0.05)。机制研究发现,沉默Piezo1导致IV型胶原及纤连蛋白表达下降。重组纤连蛋白逆转了Piezo1 sh RNA对NSCs分化的影响,即DCX阳性细胞数增加,而GFAP阳性细胞数减少。结论 综上可见,硬基底刚度通过促进Piezo1蛋白表达,上调IV型胶原及纤连蛋白表达,从而调控NSCs细胞分化。本研究为基于生物材料治疗脊髓损伤提供了新的视角。
基金supported by the Wellcome Trust,grant No.092539/Z/10/Zthe International Spinal Research Trust,grant No.STR103funded by the National Institute for Health research (NIHR) Surgical Reconstruction and Microbiology Research Centre (partnership between University Hospitals Birmingham NHS Foundation Trust,the University of Birmingham and the Royal Centre for Defence Medicine)
文摘The scarring response after a penetrant central nervous system injury results from the interaction between invading leptominingeal/pericyte-derived fibroblasts and endogenous reactive astrocytes about the wound margin. Extracellular matrix and scar-derived axon growth inhibitory mole- cules fill the lesion site providing both a physical and chemical barrier to regenerating axons. Dec orin, a small leucine-rich chondroitin-dermatan sulphate proteoglycan expressed by neurons and astrocytes in the central nervous system, is both anti-fibrotic and anti-inflammatory and attenu- ates the formation and partial dissolution of established and chronic scars. Here, we discuss the potential of using Decorin to antagonise scarring in the central nervous system.
文摘目的:探讨损伤控制手术(damage control operation)治疗兔脊髓压迫性损伤的效果。方法:应用球囊压迫法制备新西兰大白兔脊髓压迫损伤模型45只,造模术后2d随机取5只完成行为学观测、评分后取出损伤区脊髓组织进行流式细胞仪凋亡细胞检测、病理学观察、免疫组化染色检测兔损伤区脊髓组织中基质金属蛋白酶2(MMP-2)表达(对照组),剩余40只随机分为两组,每组20只,一组采用损伤控制手术(A组),即减压术前先将球囊内压力减为原来一半,使椎管内有效容积增加后再自远离脊髓压迫较重的一侧进行全椎板减压;另一组直接予全椎板切除减压,减压自压迫最严重部位开始(B组),两组减压完毕后均取出球囊,并在减压术后1d、3d、7d、14d分别随机取5只实验兔完成以上检测内容。结果:对照组造模术后48h的Tarlov评分为1.20±0.45分,A、B组减压术后1d时Tarlov评分与对照组比较均无统计学差异(P>0.05);A、B组减压术后1d、3d、7d时的Tarlov评分均无统计学差异(P>0.05),减压术后14d时A组高于B组(P<0.05)。对照组脊髓细胞凋亡率为(2.66±1.40)%,A、B组减压术后1d时脊髓细胞凋亡率均低于对照组(P<0.05);减压术后1d、3d时A、B两组损伤区脊髓细胞凋亡率无统计学差异(P>0.05);A、B组减压术后1d与3d、7d与14d损伤区脊髓细胞凋亡率无统计学差异(P>0.05);A、B组减压术后3d与7d损伤区脊髓细胞凋亡率均有统计学差异(P<0.05);减压术后7d、14d时A组损伤区脊髓细胞凋亡率均低于同时间点B组(P<0.05)。病理学观察显示对照组白质轻度脱髓鞘、部分轴突空泡样变,灰质内细胞水肿,A、B组减压术后1d、3d、7d、14d白质弥漫性脱髓鞘改变及散在点状出血,灰质内细胞水肿伴神经细胞变性逐渐加重,至减压术后7d时灰质内广泛神经细胞变性,并持续到术后14d。对照组MMP-2表达阳性细胞率为(45.76±0.75)%,A、B组减压术后1d时MMP-2表达阳性率均低于对照组(P<0.05);减压术后1d、3d、7d、14d时B组MMP-2表达阳性细胞率均高于同时间点A组(P<0.05),A、B组减压术后1d、3d比较均无统计学差异(P>0.05),3d、7d,7d、14d比较均有统计学差异(P<0.05)。结论:损伤控制手术治疗兔脊髓压迫性损伤较直接减压效果好,建议对胸腰椎爆裂骨折合并脊髓压迫损伤的治疗采用损伤控制手术方案。
文摘目的探讨脊髓损伤后基质金属蛋白酶-9(MMP-9)表达变化对血脊髓屏障(BSCB)通透性的影响。方法 C57BL/6小鼠(n=68)随机分为假手术组、损伤后2 d组(S2)、损伤后7 d组(S7)和损伤后14 d组(S14),每组17只。损伤组采用改良Allen's法制作中度脊髓损伤模型。在损伤后的第2、7、14天分别对小鼠进行盲法的小鼠后肢运动功能(BMS)评分和BMS亚评分;各组小鼠腹腔注入伊文思蓝,检测BSCB通透性;采用免疫荧光法检测紧密连接蛋白(occludin)表达,采用免疫印迹法检测occludin和MMP-9表达。结果术后2 d BMS评分显著降低,BSCB通透性显著增高;术后14 d BMS评分升高(P<0.01),BSCB通透性下降(P<0.05)。术后7 d,occludin表达下调,MMP-9表达上调(P<0.05);术后14 d occludin表达上调,MMP-9表达下调(P<0.05)。结论脊髓损伤后MMP-9可能通过介导occludin表达,影响BSCB通透性改变。
