移植神经远端吻合口再处理后相关神经元GAP-43、Bcl-2和Bax的表达
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摘要
神经缺损同手内在肌功能恢复、臂丛神经根性撕脱伤一样是至今尚未有效解决的难题。自体神经移植仍是目前临床治疗的首选方法,也是其他研究周围神经缺损治疗方法的“金标准”。移植神经存在经过缺血性改变,易形成瘢痕,再生神经纤维需经过两个吻合口,易使再生神经纤维错长或被阻断在远端吻合口等缺点。除了继发性损害的不断加重,移植的神经同样面临着中枢神经元的再生修复,然而关于移植神经远端吻合口对神经元再生影响的研究,国内外报导较少。
     本实验在国内外研究的基础上,利用大鼠坐骨神经移植模型,以GAP-43、bcl-2和bax作为观察指标,通过免疫组化、RT-PCR、western-blot以及TUNEL技术,研究二次处理移植神经远端吻合口对感觉和运动神经元再生的影响。
     实验结果显示:移植神经远端吻合口二次处理后,实验组GAP-43在相应脊髓和背根神经节中再次出现表达高峰,与对照组有明显差异;实验组bcl-2和bax的比值在相应脊髓和背根神经节中的表达再次达到低值,与TUNEL检测相一致,但与对照组相比无统计学意义。
     本实验可以得出如下结论:通过二次处理移植神经远端吻合口,轴突的延长和重建可被重新诱导,给神经元提供了二次再生的能力;二次处理虽然引起了神经元的再次凋亡,但是影响较小,形态学上观察没有统计学意义。
Peripheral nerve regeneration has been a great concern of medical science studies.The first question encountered is the source of nerve transplant donor. Nerve conduit and variant nerve can't be widely used in the clinic due to a variety of difficulties.The autograft nerve transplant takes the priority in the clinic treatment,“the golden standard”measuring other peripheral nerve treatments as well.Regeneration and scar reparation are the only two means of repairing after the body tissues get injured, which coexist after the peripheral nerve injury.Ischemic in the process of nerve transplant would bring about a scar, and desmoplasia will hamper the regenerative nerve fibers to pass through the second stomas because these fibers have two stomas to pass. The apoptosis of the neuron body and secondary lesion will be following. With the development of base medicine, people get a deeper knowledge of genes and molecule.Now we find that as a result of weaker stimuli, less factors, and restraint from the external conditions, nerve regeneration declines and enters into a relative“platform stage”after undergoing a peak of repair. Whether we can find a way to protect neuron body and overcome the defect in the autograft nerve transplant, rendering new stimulus and re-activating nerve growing, will substantially propel the studies on nerve regeneration. That’s exactly what we are working at.
     The adult wistar rats were divided into the pseudo-operation group (exposure only), the control group (excision of 2cm and suture) and the experimental group(excision of 2cm and retreatment after 8 weeks). Based on the animal model of sciatic nerve transplant, the corresponding dorsal root ganglia and spinal cord (L4-L6) were taken at different time after the operation.The growth-associated protein GAP-43 is a presynaptic membrane phosphoprotein that is expressed at high levels with the growth of axone. The protein was considered related with the nerve growth, axone regeneration and synapse reconnection strongly. Immunohistochemistry, Western Blot and RT-PCR were adopted to evaluate the different expressions of GAP-43 in dorsal root ganglia and spinal cord in the different period of time.As a new type of tumor family, bcl-2 can inhibit the cellule apoptosis and prolong the activity of cellule. The survival of nerve depends on the ration of bcl-2 and bax. Immunohistochemistry was used to detect the different expressions of bcl-2, bax and their ratio to study nerve variation rules at the protein level and the molecule mechanisms of nerve cellule apoptiosis.
     TUNEL is a widely-adopted method of cellule apoptiosis studies, by which we ascertain whether the stoma retreatment could lead to another apoptosis of the corresponding spinal segment motor neuron or not.
     Results of the study
     1 The detection of the GAP-43
     1)spinal cord motor neurons: (1) the pseudo-operation group: the results show that GAP-43 in the pseudo-operation group maintains a certain level in spinal cord but only has a small amount of expressions, and shows no statistical difference over time. (2)the control group : The amount of GAP-43 in the control group increases significantly on the first week, peaks in the second week, keeps high in the fourth to the sixth weeks, and in the eighth to the sixteenth weeks it descends and stays invariable. (3)The experiment group: The amount of GAP-43 in the experiment group is the same with that in the control group in the third day to the eighth week. GAP-43 increases again from the third day after the eighth week to the twelfth week, and peaks in the tenth week again. It descends in the fourteenth to the sixteenth weeks over time.
     2)dorsal root ganglion:(1) the pseudo-operation group: the results show that GAP-43 in the pseudo-operation group maintains a certain level in spinal cord but only has a small amount of expressions, and shows no statistical difference over time. (2) the control group : GAP-43 expression has increased in the first week and reached peak in the second week after sciatic nerve transplant. It keeps high in the fourth to the sixth weeks, falls in the eighth week, and shows no statistical difference over time. (3) the experiment group: The expression of GAP-43 in the experiment group is the same with that in the control group in the third day to the eighth week, increases again from the third day after the eighth week to the twelfth week, comes to the second peak in the tenth week after the first operation, and finally falls over time in the fourteenth to the sixteenth week.
     2 The detection of bcl-2 and bax
     1) spinal cord motor neurons: chromagen was buffy and located in cytoplasm,excluding nucleus. (1)the pseudo-operation group: the immunoreactive cells stained are not found.(2) the control group : the immunoreactive cells stained shown in neuron and glioncyte on the third day after the sciatic nerve transplant, are located in cytoplasm, excluding nucleus. The expression of bcl-2 and bax increases gradually, reaches the peak in the second week, then descends little by little. (3) the experiment group: The result is the same with the control group in the third day to the eighth week. The expression increases again on the third day after the eighth week, peaks in the tenth week again, and then descends.(4) bcl-2/ bax in the control group: The ration of bcl-2/ bax falls down from the third day, comes to the lowest point in the second week, then increases little by little and stays invariable from the eighth week.(5) bcl-2/ bax in the experiment group: The ration of bcl-2/ bax is the same with the control group in the third day to the eighth week. It descends again in the third day after the eighth week, peaks in the tenth week again, and then increases. The Student’s test results show no statistical significance over time.
     2) dorsal root ganglion:chromagen was buffy and located in cytoplasm ,excluding nucleus.(1) pseudo-operation group: the immunoreactive cells stained are not found.(2) the control group : the immunoreactive cells stained shown in neuron and glioncyte on the third day after the sciatic nerve transplant, are located in cytoplasm ,excluding nucleus . The expression of bcl-2 and bax increases gradually, reaches the peak in the second week, and then descends little by little. (3) the experiment group: The expression is the same with the control group on the third day to the eighth week. After that, it increases, peaks in the tenth week again, and then descends.(4) bcl-2/ bax in the control group: The ration of bcl-2/ bax falls down from the third day, comes to the lowest point in the second week, and then increases little by little.(5) bcl-2/ bax in the experiment group: The ration of bcl-2/ bax is the same with the control group onn the third day to the eighth week. After it, it descends, peaks in the tenth week again, then increases. The Student’s test results show no statistical significance over time compared with the control group.
     3 The detection of TUNEL
     1) the control group: The electropositive cells are microamount on the third day, and becomes dense in the second week, when the number density of apopotosis comes to the peak, and then descends obviously from the third day after the eighth week and the tenth week.2) the experiment group: it is the same with the control group on the third day and in the second week, but it becomes more in the tenth week than on the third day after the eighth week. There is no statistical significance in the apopotosis cell over time.
     Conclusion:In the rat model of sciatic nerve transplant, after surgical removal and renovation of the distal stoma of transplant nerves, elongation and reconstruction of an axon can be induced again, and then transcription and translation of growth-associated protein gene are stimulated, thus GAP-43 arrives at the second peak. The expression of bcl-2 and bax coincides with apoptosis following the nerve regeneration. The change of bax/bcl-2 ratio determines the neurocytes to survive or die following the nerve regeneration. The surgical removal and renovation of the distal stoma induce the neurocytes apoptosis, but have little effect. There is no statistical significance on morphology observation. This method can not only stimulate the regeneration of the neuron body but also release the scar restraint for nerve regeneration, which displays the reparation unity of neural body, neurite and microenvironment, and thus offers a new scientific idea and technique for the reinforcement of nerve transplant.
引文
[1]Femandez VC,Bunge Rp,Bunge MB.Schwann cells degrade myelin and proliferate in the absence of maorophages:evidence frorm in vitro studies of Wallerian degenerotion [J].J Neurocytol,1995,24(9):667-679.
    [2]Rath EM,Kelly D,Bouldin TW,et al. Impaired peripheral nerve regenration.in a mutant strain of mice (Enr) with a Schwann cell defect [J].J Neurosci 1995,15(11):7226-7237.
    [3]Stoll G,Griffin JW,Li CY,et al.Wallerian degeneration in the peripberal nervous system:participation of both Schwann cells and macrophages in myelin degeneration.J Neuroeytol,1989,18:671-683.
    [4]Wheeler EF,Naftel JP,Pan M,et al.Neurotrophin receptor expression is induced in a subpopulation of trigeminal neurons that label by retrograde transport of NGF or fluoro-gold following tooth injury. Brain ResMol Brain Res,1998,61:23-38.
    [5]Barde YA.Trophic factors and neuron survival.Neuron,1989;2:1525-1534.
    [6]Raff MC,Barres BA,Burne JF,et al.Programmed cell death And the control of cell survival:lesions from the nervous system.Science,1993;262:695-699.
    [7]Longo FM,Skaper SD,Manthorpe M,et al.Temporal Changes of neuronotrophic activities accumulating in vivo with in nerve regeneration chambers. Exp Neurol,1983;81:756-769.
    [8]Fu SY,Gordon T.The Cellular and molecular basis of peripheral Nerve regeneration [J].Mol Neurobiol,1997,14(1-2):67-116.
    [9]Lundborg G,DahlinL,Danielsen N,et al.Trophism,tropism and specificity in nerve regeneration. J Reeonst Microsurg,1994;10:345-354.
    [10]王国英,平井圭一,钟世镇.雪旺氏细胞基底膜成份_Laminin在神经再生中的作用探讨,中国临床解剖学杂志,1992;10:200-207.
    [11]Kuffler DP. Promoting and directing axon outgrowth. MolNeurobiol. 1994;9:233-243.
    [12]Bixby JL,Bookman RJ. Intracellular mechanisms of axon growth induction by CAMs and integrins:some unresolved issues. Perspect Dev Neurobiol,1996,4:147-156.
    [13]Hirokawa N. Molecular architecture and dynamics of the neuronal cytoskeleton.In:Burgoyne R D,ed.The Neuronal Cytskeleton.New York:Wiley Liss,1991,5-74.
    [14]Hirokawa N. Miceotubuleorganization and dynamics dependent on microtubule–associated proteins.Curr Opin Cell Biol,1994,6:74-81.
    [15]Tǒgel M,Wiche G,Propst F.Novel features of the light chain of microtubule-associated protein MAP1B:microtubule stabilization,self-interaction,actin filanent binding andregulation by heavy chain.J Cell Biol,1998,143:695-707.
    [16]Zheng M,Kuffler DP.Guidance of regenerating motor axons in vivo by gadients of diffusible peripheral nerve-derived faetors [J].J Neurobiol,2000,42(2):212-219.
    [17]Black MM,Slaughter T,Fischer I.Microtubule-assoeiated protein lb (MAPlb) is concentrated in the distal region of growing axons[J].J Neurosci,1994,14(2):857-870.
    [18]Goold RG,OwenR,Gordon-WeeksPR. Glycogen synthase kinase 3beta phosphorylation of microtubule-associated protein 1B regulates the stability of microtubules in growth cones.J Cell Sci. 1999 Oct;112 ( Pt 19):3373-3384.
    [19]Meixner A,Haverkamp S,Wassle H,et al. MAP1B is required for axon guidance and is involved in the devdlopment of the central and peripheral nervous system. J Cell Biol,2000 Dec 11;151(6):1169-1178.
    [20]Ramon-Cueto A,Avila J Two modes of microtuble-associated protein1B phosphorylation are differentially regulated during perlpheral nerve regeneration[J].Brain Res,1999, 815 (2):213-226.
    [21]George R,Griffin JW. Delayed macrophage responses and myelin clearance during Wallerian degeneration in the central nervous system:the dorsal radiculotomy model. Exp Neurol,1994,129:225-236.
    [22]Wang J,Chako J,Battisti W,et al.The response of non-neuronal cells to optic nerve injury in goldfish.Abstracts of 21th Annual Meeting,New Orleans:Louisana,1991:10-15.
    [23]Beuche W,Friede RL.The role of non-resident cells in Wallerian degeneration.J neurocytol,1984;13:767-796.
    [24]Saada A,Reichert F,Rotshenker S. Granulocyte macrophage colony stimulating factor produced in lesioned peripheral nerves induces the up-regulation of cell surface expression of MAC-2 by macrophages and Schwann cells. J Cell Biol,1996,133:159-167.
    [25]Bruck W,Friede RL.Anti-macrophage CR3 antibody blocks myelin phagocytosis by macrophages in vitro.Acta Neurophath,1990;80:415-418.
    [26]Carnmer W,Bloom BR,Norton WT et al. Degradation of basic protein in myelin by proteases secreted by activated macrophages:A possible rnachanism of inflammarory demyelinarion.Proc Natl Acad Sci USA,1978;75:1554-1558.
    [27]Rich KM,YipHK,Osborne PA,et al.Role of nerve growth factor in the adult dorsal root ganglia neuron and its response to injury.J Comp Neurol,1984,230:110.
    [28]许家军,何成,宋田斌,等.周围神经损伤后外源性神经生长因子及睫状神经营养因子对神经元的保护作用.中华显微外科杂志,1997,20:32-35.
    [29]刘红光,洪光祥,王发斌,等.周围神经损伤后背根神经节神经元合成抗氟化物酸性磷酸酶的变化及其保护作用.中华实验外科杂志,1998,15:267-268.
    [30]Xi-Nan Yi,Lin-Feng Zheng,Jian-Wei Zhang, et al. Dynamic changes in Robo2 and Slit1 expression in adult rat dorsal root ganglion and sciatic nerve after peripheral and central axonal injury.Neuroscience Research 56 (2006) 314–321.
    [31]吴燕,米瑞发,刘红,等.损伤坐骨神经后脊髓腹角运动神经元中α管蛋白的免疫组化研究.解剖科学进展,1997,3:281.
    [32]Curtis R,Tonra JR. Neuronal injury increases retrograde axonal transport of the neurotrophins to spinal sensory neurons and motor neurons via multiple receptor mechanisms. Mol Cell Neurosci,1998,12(3):105-118.
    [33]Yan Q,Johnson EM. An immunohistchemical study of the nerve growth factor receptor in developing rats. J Nrurosci,1998,8:3481-3485.
    [34]杨青峰,陈彪,杨宏,等.大鼠脊髓组织CNTFR mRNA的表达及其坐骨神经伤后表达的变化.军事医学科学院院刊,1998,22:84-87.
    [35]Yamada M,Natsume A,Mata M,et al.Herpes simplex virus vector-mediated expression of Bcl- 2 protects spinal motor neurons from degeneration following root avulsion [J].Exp Neurol,2001,168(2):225-230.
    [36]Natsume A,Mata M,Wolfe D,et al.Bcl-2 and GDNF delivered by HSV-mediated gene transfer after spinal root avuision provide a synergistic effect [J]. Neurotrauma, 2002,19 (1)
    [37]Mattsson P,Aldskogius H,Svensson.Nimodipine-induced improved survival rate of facial motor neurons following intracranial transection of the facial nerve in the adult rat.J Neurosurg,1999,90(4):760-765.
    [38]Casanovas A,Ribera J,Hukkanen M,et al.Prevention by lamotrigine,MK-801 and N omega-nitro-L-arginine methyl ester of motoneuron cell death after neonatal axotomy. Neuroscience,1996,71(2):313-325.
    [39]Iwasaki Y,Ikeda K.Prevention by insulin-like growth factor-Ⅰand riluzole in motor neuron death after neonatal axotomy.J Neurol Sci,1999,169(1-2):148-155.
    [40]Smith SL,Oostveen JA,Hall ED.Two novel pyrrolopyrimidine lipid preoccupation inhibitors U-101033E and U-104067F protect facial motor neurons following neonatal axotomy.Exp Neurol,1996,141(2):304-309.
    [41]蔡卫华,贾连顺,叶晓健,等.甲基强的松龙对脊髓损伤后伤段脊髓线粒体功能的影响[J].中国脊柱脊髓杂志,2005,15(12):749-752.
    [42]Ludwig A,Pico C.Depltion of 43-KD Growth -associated Protein in Primary Sensory Neurons Leads to Diminished Formation and Spreading of Growth Cones.J Cell Biol, 1993;123:417.
    [43]Larry IB,Aryeh R. GAP-43:an intrinsic determinant of neuronal development and plasticity. TINS,1997; 20(2):84.
    [44]Basi GS,Jacobson RD, Virag I,Schilling J, Skene JH. Primary structure and transcriptional regulation of GAP-43, a protein associated with nerve growth.Cell. 1987 Jun 19;49(6):785-91.
    [45]严恒林.生长相关蛋白(GAP-43)与神经发育和再生.神经解剖学杂志, 1993;9 (2):155.
    [46]Arvidsson J,Ygge J, Grant G.Cell loss in lumbar dorsal root ganglia and transganalionic degeneration after sciatic nerve resection in the rat.Brain Res. 1986 May 14;373 (1-2):15-21.
    [47]杨辉综述. GAP-43表达与神经元生长、可塑性的关系.国外医学生理、病理科学与临床分册,1995;15 (2):117-119.
    [48]许建中,李起鸿.生长相关蛋白-43与周围神经损伤及再生.中华创伤杂志, 1999;15(5):391.
    [49]Brook GA Schmitt AB, Nacimiento W, et al. Distribution of B-50(GAP-43 mRNA and protein in the normal adult human spinal cord.Acta Neuropathol Berl, 1998;95(4): 378.
    [50]Davies SJ,Fitch MT.Memberg SP,et al.Regeneration of adult axon in white matter tracts of the central nervous system.Nature,1997,390:680-683.
    [51]Tolner EA,Vliet EA,Holtmaat AJ,et al.GAP-43 mRNA and protein expression in the hippocampal and parahippocampal region during the course of epileptogenesis in rats [J] . Eur Neurosci,2003,17:2369-380.
    [52]Mason MR,Lieberman AR,Anderson PN.Corticospinal neurons up-regulate a range of growth-associated genes following intracortical,but nor spinal,axotomy. Eur J Neurosci,2003,18:789-802.
    [53]Kawasaki T,Nishio T,Kawaguchi S,et al.Spatiotemporal distribution of GAP-43 in the developing rat spinal cord:a histological and quantitative immunofluorescence study. Neurosci Res,2001,39:347-358.
    [54]Naffah-Mazzacoratti M,Funke MG,Sanabria ERG,et al.Growth–associated phospho- protein expression is increase in the supragranular region of the dentategyrus following pilocarpine-induced seizures in rats[J].Neuroscience,1999,91(2):485-492.
    [55]Luque JM,Puign,Martinez JM,et al.Glutamate N-methy L-D-aspartate receptor blockadeprevents induction of GAP-43 after focal ischemia in rats[J].Neurosci Lett,2001, 305 (2):87-90.
    [56]McIlvain VA,Robertson DR,Maimone MM ,et al.Abnormal thalamocortical pathfinding and terminal arbors lead to enlarged barrels in neonatal GAP-43 heterozygous mice [J].CompNeurol,2003,462(2):252-64.
    [57]Gajda M,Adriaensen D,Cichocki T. Development of the innervation of long bones:expression of the growth-associated protein 43.Folia Histochem Cytobiol, 2000; 38: 103-10.
    [58]Dubroff JG,Stevens RT,Hitt J,et al. Anomalous functional organization of barrel cortex in GAP-43 deficient mice [J]. Neuro-Image,2006,29(4):1040-1048.
    [59]Zhu QZ,Julien JP. A key role for GAP-43 in the retinotectal topographic organization [J]. Exp Neurol,1999,155(2):228-242.
    [60]覃华丽,周雪,章为.生长相关蛋白GAP-43的研究现状[J].四川解剖学杂志,2002,10(2):78-83.
    [61]DeGraan PN,Hens JJ,Gispen WH.Presynaptidc PKC substrate B-50(GAP-43) and neurotransmitter release :studies with permeated synaptosomes Neurotoxicology. 1994 Spring;15(1):41-47.
    [62]Donovan SL,Mamounas LA,Andrews AM,et al .GAP-43 is criticalfor normal development of the serotonergic innervation in forebrain.J Neuro sci ,2002,22(9):3543.
    [63]Larry IB,Aryeh R. A membrane phosphoprotein associated with neural Development, axonal regeneration,phospholipid metabolism and synaptic plasticity. TINS,1987; 10(12): 527.
    [64]Skene JHP. Axonal Growth-Associated Proteins. Ann Rev Neurosci,1989;12:127.
    [65]Biewenga JE,Schrama LH,Gispen WH. Presynaptic phosphoprotein Gap-43/B-50 in neuronal and synaptic plasticity.Acta Biochim Por,1996;43:327-38.
    [66]Gerendasy D. Homeostatic tuning of Ca2+ signal transduction by members of the calpacitin protein family. J Neurosci Res, 1999;58 (1):107.
    [67]Esdar C,Oehrlein SA,Reinhardt S,et al. The protein kinase C (PKC) substrate GAP-43 is already expressed in neural precursorcells,colocalizes with PKCeta and binds calmodulin. Eur J Neurosci,1999;11(2):503.
    [68]Neve RL,Coopersmith R,McPhie DL,et al. The neuronal growth-associated protein GAP-43 interacts with rabaptin-5 and participates in endocytosis. J Neurosci, 1998; 18(19):7757.
    [69]Lu J,Ashwell KW,Waite P.Advances in secondary spinal cord injury:role of apoptosis[J].Spine,2000,25(14):1859-1866.
    [70]Snider WD,ThanedarS .Target dependence of hypoglossal motor neurons during development and in maturity.J ComP Neurol,1989,279:489-498.
    [71]Sendtdner M,Kreutzberg GW,Thoenen H.Ciliary neurotrophic factor prevents the degeneration of motor neurons after axotomy.Nature,1990,345:440-441.
    [72]Phelan KA,Hollyday M.Embryonic development and survival of brachial motoneurons projecting to muscless chick wings.J Comp Neurol,1991,311:313-320.
    [73]Sulpice JC,Zachovisk A,Devanx DF, et al. Requirement for phosphatidy linositol 4,5-bisphosphate in the Ca2+-induced phospholipid redistribution in the human erythrocyte membrance[J].J Biol Chem,1995,269(12):6347-6354.
    [74]李涛,徐汉宫.溴氰葡酯对大鼠神经细胞内游离钙浓度及凋亡的影响[J].中华劳动卫生职业病杂志,2002,20(6):427-429.
    [75]彭黎明,王曾礼.细胞凋亡的基础与临床[M].北京:人民卫生出版社,2000:41-91.
    [76]Schulz JB,Beinroth S,WellerM, et al. Endonucleolytic DNA fragmentation is not required for apoptosis of cultured rat cerebellar granule neurons. Neurosci Lett,1998,245:9-12.
    [77]Aronica EM,Gorter JA,Grooms S,et al. Aurintricarboxylic acid prevents GLUR2 mRNA down-regulation and delayed neurodegeneration in hippocampal CA1 neurons of gerbil after global ischemia. Proc Natl Acad Sci USA,1998,95:7115-7120.
    [78]王贵波,李兵仓,王建民,等.兔坐骨神经火器伤后腰段脊髓脂质过氧化反应及意义.中国急救医学,2002,22:1-3.
    [79]Love S. Oxidative stress in brain ischemia.Brain Pathol,1999,9:119-131.
    [80]Fraser A,Evan G.A license to kill.Cell,1996,85(6):781-784.
    [81]Masayuki M,Zhu H,Rrotello R,et al. Introduction of apoptosis in fibroblasts by IL-1β-converting enzyme, a mammalian homolog of the C. Elegans cell death gene ced-3[J]. Cell,1993,75:653-655.
    [82]Thornberry N A,Lazebnik Y. Caspases:Enemies Within[J]. Science, 1998,281:1312 -1316 .
    [83]Enari M,Sakahira H,Yokoyama H,et al. A Caspase-activated DNase that degrades DNA during apoptosis and its inhibitor ICAD[J]. Nature,1998,391:43-50.
    [84]Mukae N,Enari M,Sakahira H,et al.Proc Natl Acad SciU S A,1998,95(16):91-93.
    [85]Lo AC,Houenou LJ,Oppenheim RW. Apoptosis in the nervous system:morphological features,methods,pathology and prevention. Arch Histol Cytol,1995,58:139-149.
    [86]Wijsman JH,Jonker RR,Keijzer R,et al. A newmethod to detect apoptosis in paraffinsections:in situ end-labelling of fragmented DNA.J Histochem Cytochem,1993 ,41:7-12.
    [87]Garrah JM,Bisby MA,Rossiter JP. Immunolabelling of the cytoplasm and processes of apoptotic facial motoneurons following axotomy in the neonatal rat. Acta Neuropathol Berl,1998,95:223-228.
    [88]Sheridan JP,Marsters SA,Pitti RM, et al. Control of TRAIL-induced apoptosis by a family of signaling and decoy receptors (see comments).Sci,1997,277:818-821.
    [89]De Maria R,Lentil L,Malisan F,et al. Requirement for GD3 ganglioside in CD95- and ceramide-induced apoptosis. Sci,1997,277:1652-1655.
    [90]Machleidt T,Kramer B,Adam D,et al.Function of the P55 tumor necrosis factor receptor“death domain”mediated by phosphatidyl-choline-specific phospholipase C.J Exp Med.1996,184:725-733.
    [91]Beg AA,Baltimore D,Zhou Q,et al. An essential role for NF-kappa B in preventing TNF-alpha-induced cell death (see comments). Sci,1996,274:728-784.
    [92]Chinnaiyan AM,O’Rourke K,Yu GL,et al. Signal transduction by DR3,a death domain-containing receptor related to TNFR-1 and CD95.Sci,1996,274:990-992.
    [93]Marsters SA,Sheridan JP,Pitti RM,et al. Identification of a ligand for the death-domain-containing receptor Apo3.Curr Biol,1998,8:525-528.
    [94]Grusch M,Polgar D,Gfatler S,et al.Maintenance of ATP favours apoptosis over necrosis triggered by benzamide riboside[J].CELL Death Differ,2002,9(2):169-178.
    [95]Machleidt T,Kramer B,Adam D,et al.Function of the P55 tumor necrosis factor receptor“death domain”mediated by phosphatidyl-choline-specific phospholipase C.J Exp Med,1996,184:725-733.
    [96]Pan G,Ni J,Wei YF,et al. An antigonist decoy receptor and a death domain-containing receptor for TRAIL(see Comments). Sci,1997,277:815-818.
    [97]刘京升,孙正义.神经生长因子及其受体与周围神经损伤[J].中华微创外科杂志,2002,2(6):440-441.
    [98]张晓,李爱冬,王廷华,等.坐骨神经切断后脊髓神经细胞的凋亡变化[J].中国临床康复,2003,7(2):202-203.
    [99]张燕青,曾园山.雪旺细胞移植对中枢神经再生的影响[J].解剖学研究,2000,22(2):142-145.
    [100]谢冈,朱家恺,顾熊飞.雪旺细胞浆神经营养蛋白高效液相分离纯化及其生物活性研究[J].中国修复重建外科杂志,2000,14(4):226-229.
    [101]Steuer H,Fadale R,Muller E.et al.Biohybride nerve guide for regeneration;Degradable polylactide fibers coatel with rat Schwann dells Nenrosci lett 1999,277(3):165-167.
    [102]Hadlock T,Sundback C,Hunter D,et al.A polymer foam conduit seeded with Scjwamm cells promotes guided peripheral nerve regeneration.Tissue Eng2000;6(6):119-200.
    [103]许小珊.周围神经的生理及损伤病理.见:朱盛修.周围神经显微修复学[M].北京:科学出版社,1991,23-47.
    [104]Lundborg G.Nerve regeneration and repair.Acta OrthopScand,1987,58:145-169.
    [105]Lundborg G. Nerve regeneration problems in a clinical perspective.Restor Neurol Neurosci,1990,l:297.
    [106]李玉林,主编.病理学(第六版) [M].北京:人民卫生出版社,2003,25-39.
    [107]佟晓杰.周围神经再生及其影响因素[J].现代康复,2000,4(10):1444-1445.
    [108]Jacob S,Martin K.The initial period of peripheral nerve regeneration and importance of the local environment for the conditioning lesion effect[J],Brain Res,1990,529:79-84.
    [109]Kwon BK,Liu J,Oschipok L,et al.Reaxotomy of chronically injured rubrospinal neurons results in only modest cell loss.Exp Neurol,2002,177:332-337.
    [110]Brock TO 3rd,Tumer JE,Retinal ganglion cell body resonse to repeated axotomy in the regenerating visual system on newt(Notophthalmus biridescens).Exp Neurol.1982, 78:316-330.
    [111]McPhail LT,Femandes KJ,Chan CC,et al.Axonal Reinjury reveals the survival and re-expression of regeneration-associated genes in chronically axotomized adult mouse motoneurons.Exp Neurol,2004,188:331-340.
    [112]Benowitz,L.I.and A.Routtenberg.GAP-43:an intrinsic determinant of neuronal development and plasticity.Trends in Neurosei.1997,20:84-91.
    [113]余茜,李晓红,经皮电刺激促进坐骨神经损伤大鼠脊髓GAP-43mRNA的表达.[J].泸州医学院学报,2001,24(5):386.
    [114]Hoffman,P.N.et al.Expression of GAP-43,a rapidly transported Growth-associted Protein,and classⅡbeta-tubulin,a slowly transported Cytoskeletal protein,are coordinated in regenrating neurons[J].Neurosei,1989,9:893-897.
    [115]刘光久,李振强,殷玉芹,等.神经损伤与再生中GAP-43mRNA表达和蛋白合成的实验研究[J].第三军医大学学报,2002,24(3):283-285.
    [116]Strittmatter SM,Vartanian t,Fiabman MC.GAP-43 as a plasticity protein in neuronal form and repair[J].J Neurobiol,1992,23(5):507-520.
    [117]Alexander KA,Wakim BT,Duyle GS et al.Indentification and characterization of the calmodulin-binding domain of neuromodulin a neurospecific calmodulinbinding protein [J].J Biol Chem,1988,263(16): 7544-7549.
    [118]Harada H,Grant S.Apoptosis regulators [J].Rev Clin Exp Hematol,2003,7(2):117-138.
    [119]Lebedeva IV,SarkarD,Su ZZ,et al.Bcl-2 and Bcl-x(L) differentially protecthuman prostate cancer cells from induction of apoptosis by melanom a differentiation associated gene-7,mda-7 /IL-24 [J].Oncogene,2003,22(54):8758-8773.
    [120]Hou Q,Cymbalyuk E,Hsu SC,et al. Apoptosismodulatory activities of transiently expressed Bcl-2:Roles in cytochrome C release and Bax regulation [J].Apoptosis, 2003,8(6):617-629.
    [121]Kerr JF.Wyllie All.Currie-AR.Apoptosis:A basic biological phenomenon with wide- ranging implications in tissue kinetics.Br J Caneer,1972,26:239.
    [122]Oliveira AL,Risling M,Deckner M,et al.Neonatal sciatic nerve transection induces TUNEL labeling of neurons in the rat spinal cord and DRG. Neuroreport, 1997, 8 (13):2837-2840.
    [123]Ekstrom PAR. Neurones and glial cells of the mouse sciatic nerve undergo apoptosis after injury in vivo and in vitro.Neuroreport, 1995,6(7):1029-1032.
    [124]Wiese,U.H.and Ruth,J.L.Differential expression of growth-associated protein (GAP-43) mRNA in rat primary sensory neurons after peripheral nerve lesion:a non-radioactive in situ hybridization study.Brain Researeh.1992,592:141-156.
    [125]Wiese,U.H.and Emson,P.C.Expression of growth-associated protein(GAP-43)mRNA in adult normal and axotomized rat lumbar primary sensory neurons[J]. Physiol. 1992,446:305.
    [126]陈晓东,顾玉东,徐建光.损伤大鼠坐骨神经诱导运动神经元凋亡的初步报告[J].中华手外科杂志,1999,15(2):111-113.
    [127]齐巍,程爱国,刘昊,等.妥乐平对大鼠坐骨神经损伤后脊髓运动神经元的保护作用[J].中国康复理论与实践,2008,14(8):703-704.

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