MMP-2、MMP-9及TIMP-1在颅内动脉瘤中的表达及意义
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摘要
目的:
     通过观察基质金属蛋白酶-2(MMP-2)、基质金属蛋白酶-9(MMP-9)和基质金属蛋白酶抑制剂-1(TIMP-1)在颅内动脉瘤中的表达情况,并且与正常颅内动脉的表达相比较,为研究颅内动脉瘤的发病原因及机制提供思路。
     方法:
     收集南昌大学第一附属医院2009年10月-2010年7月之间经开颅手术,夹闭动脉瘤后切取的颅内动脉瘤标本31例,其中前交通动脉瘤(ACA)13例,大脑中动脉动脉瘤(MCAA)8例,后交通动脉瘤(PCA)6例,椎动脉动脉瘤(VSA)2例,大脑前动脉动脉瘤2例。正常对照组的16例动脉血管均来自我科同期行颅内血肿清除的脑外伤病人已经离断的动脉血管。其中颞浅7例,脑膜中动脉4例,脑皮层动脉5例。将所得染色标本在光镜下观察颅内动脉瘤壁的镜下病理结构特征。用免疫组化方法比较颅内动脉瘤壁与正常颅内动脉壁中的MMP-2、MMP-9、TIMP-1的表达情况。
     结果:
     1.肉眼观察:动脉瘤夹闭前呈浆果状,切除后动脉瘤呈紫褐色、暗红色或灰色。部分动脉瘤瘤腔内有血栓,有些出现机化和钙化。瘤壁厚薄不一,顶部较基底部薄,多数瘤壁由很薄的纤维组织构成,呈半透明状。质地不均,有的松软,有的较硬。
     2.HE染色:动脉瘤瘤壁很难分辨内膜、中膜和外膜。均丧失了正常脑动脉壁的三层结构。尤其表现在内膜和中膜。内弹力层几乎全部消失,内皮细胞减少,连续性中断。可见血栓形成及部分血栓机化。中膜层正常结构消失,平滑肌萎缩,平滑肌细胞大量减少甚至消失。被大量的纤维组织填充,增生的纤维组织排列紊乱。外膜层较薄,主要为纤维组织,无外弹力层。瘤壁各层均可见到不同程度的炎性细胞浸润,主要为巨噬细胞和淋巴细胞。瘤壁呈现动脉硬化样改变,见细胞内脂质沉积,主要出现在内膜层和中膜层。
     3.免疫组化染色结果:MMP-2、MMP-9在颅内动脉瘤壁中高表达,分别为87.10%(27/31)、80.65%(25/31),在内、中、外膜均有表达,而对照组中均无表达,差异有统计学意义。TIMP-1在颅内动脉瘤壁和对照组中的阳性率分别为87.10%(27/31)和56.25%(9/16),差异有统计学意义。
     结论:
     1.颅内动脉瘤的病理学改变主要是内弹力层几乎全部消失,平滑肌萎缩,平滑肌细胞大量减少,外膜层较薄,瘤壁各层均可见到不同程度的炎性细胞浸润,主要为巨噬细胞和淋巴细胞。
     2. MMP-2、MMP-9及TIMP-1在颅内动脉瘤瘤壁各层均有表达,颅内动脉瘤中MMP-2、MMP-9、TIMP-1表达明显增高。
     3.MMP-2、MMP-9与TIMP-1与颅内动脉瘤密切相关,可能是MMPs与TIMPs共同维系的细胞外基质新陈代谢的动态平衡发生失衡与颅内动脉瘤的发生密切相关,具体机制有待今后进一步的研究。
Objective:
     To examine the expression of matrix metalloproteinases-2 (MMP-2)、matrix metalloproteinases-9 (MMP-9) and Matrix metalloproteinase inhibitor-1 (TIMP-1) in intracranial aneurysms and compare them with those exp ressed in normal brain vessels tissue. To hope to obtain useful informations for better understanding of the pathogenesis of intracranial aneurysms.
     Methods:
     Thirty-one surgical specimens of human cerebal aneurysm in the First Affiliated Hospital of Nanchang University during Oct,2009 to July,2010 were choosen.All specimens were got from dissecting after clinpping the aneurysm in craniotomy.Including 13 of cases anterior communicating aneurysms,8 cases of middle cerebral artery aneurysms,6 cases of posterior communicating aneurysms,2 cases Aneurysm of vertebral artery,2 cases of anterior cerebral artery aneurysms.Sixteen control specimens including 7 cases of superficial temporal artery,4 cases of middle meningeal artery, and 5 cases of pial artery.These specimens came from hematoma removal and internal decompression.To observe the expression of MMP-2,MMP-9 and TIMP-1 in human cerebral aneurysm with immunohistochemical method.
     Results:
     1.Naked eyes observation:The aneurysms look like berry before clipping.Most specimens were dark brown、dark red and gray.There were thrombosis in some cavities of the aneurysms. Calcification could be seen in some of the aneurysms specimens.The wall of the aneurysms were various,the top were thinner than the basilar part.Most aneurysms were made of thin fibrous tissue.texture were various,some were soft.and some were stiff.
     2.HE staining:It is difficult to distinguish the tunica interna、the tunica media and the tunica externa.The three-layered structure of normal brain artery wall were lost. Internal elastic layer almost disappeared,and endothelial cell were reduced, thrombosis and part organization could be seen.The normal structure of tunica media layer were disapeared. smooth muscle atrophied and smooth muscle cell were reduced even disapeared.were filled with fibrous tissue,and the fibrous tissue arrange disord. Tunica externa layer were thin, mainly fibrous tissue, no external elastic layer. Inflammatory cell infiltrate could be seen in every layer of the aneurysms wall, mainly macrophages and lymphocytes.The aneurysmal wall showed atherosclerosis-like changes, lipidoses could be seen in the cell,mainly in the tunica interna and tunica media.
     3.The immunhistochemistry staining:The high expression of MMP-2, MMP -9 in human cerebal aneurysmal walls,were 87.10%(27/31) and 80.65% (25/31),MMP-2、MMP-9 expressed in tunica interna、tunica media and tunica externa.But no erpression of MMP-2、MMP-9 in control group, indicating the statistical significance.The positive rate of TIMP-1 in human cerebal aneurismal walls and control group were 87.10%(27/31) and 56.25%(9/16), indicating the statistical significance.
     Conclusions:
     1.The pathological changes of intracranial aneurysms mainly internal elastic layer almost disappeared,and endothelial cell were reduced and Tunica externa layer were thin. Inflammatory cell infiltrate could be seen in every layer of the aneurysms wall. Mainly macrophages and lymphocytes.
     2.The high expression of MMP-2,MMP-9 and TIMP-1 in human cerebal aneurismal walls,they express in every layer.
     3.MMP-2,MMP-9 and TIMP-1 were closely related with intracranial aneurysms, maybe MMPs and TIMP common to maintain the homeostasis of extracellular matrix metabolism occurrence imbalance were closely to related intracranial aneurysm. Specific mechanism needs further research.
引文
[1]Rinkel GJ, Djibuti M, Algra A, et al. Prevalence and risk of rupture of intracranial aneurysms: a systematic review. Stroke 1998; 29:251-6
    [2]Gasparotti R, Liserre R. Intracranial aneurysms. Eur Radiol 2005; 15:441-7
    [3]Polmear A. Sentinel headaches in aneurysmal subarachnoid haemorrhage:what is the true incidence? A systematic review.Cephalalgia 2003; 23:935-41
    [4]Fergusen S, Macdonald RL. Predictors of cerebral infarction in patients with aneurysmal subarachnoid hemorrhage. Neurosurgery.2007;60:658-667
    [5]Tipper G, U-King-Im JM, Price SJ, et al. Detection and evaluation of intracranial aneurysms with 16-row multislice CT angiography. Clin Radiol 2005;60:565-72
    [6]Kouskouras C, Charitanti A, Giavroglou C, et al. Intracranial aneurysms:evaluation using CTA and MRA. Correlation with DSA and intraoperative findings. Neuroradiology 2004; 46:842-50
    [7]Tummala RP, Baskaya MK, Heros RC. Contemporary management of incidental intracranial aneurysms. Neurosurg Focus 2005; 18:9:1-7.
    [8]干忠诚,赵继宗等,王忠诚神经外科学:湖北科学技术出版社,2005:759-762
    [9]Baker CJ, Fiore A, Connolly S, et al. Serum elastase and alpha-1-antitrypsin levels in patients with ruptured and unruptured cerebral aneurysms. Neurosurgery.1995;37:56-62
    [10]Hashimoto T, Meng H, Young WL. Intracranial aneurysms:Links between inflammation, hemodynamics and vascular remodeling. Neurol Res.2006;28:372-380
    [11]Shi C, Awad IA, Jafari N,et al. Genomics of human intracranial aneurysm wall. Stroke. 2009;40:1252-1261
    [12]Yoshitsugu Nuki, Tsung-Ling Tsou, Chie Kurihara,et al. Elastase-induced intracranial aneurysms in hypertensive mice. Hypertension.2009;54(6):1337-1344
    [13]Kataoka K,Taneda M,Asai T,X.Sturctural fragility and inflammatory response of ruptured cerebral aneurysm :a comparative study between ruptures and unruptured cerebral aneurysms[J].Stroke,1999,30:1396-1401
    [14]Pfefferkorn T,Rosenberg GA,Closure of the blood-brain barrier by matrix metalloproteinase inhibition reduces rtPA-mediated mortality in cerebral ischemia with delayed reperfusion, Stroke,2003,34:63-68.
    [15]Pendas AM,Knauoer V,Puents XS,et al.Idenfication and characterization of a novel huaman matrix metaloproteinase with unique structural characteristic,chromosomal location,and tissue distibution[J].J Biol Chem,1997,272(7):4281-4286.
    [16]Toschi E, Barillari G. Sga dari C. et al. Activation of matrix-metlloproteinase-2 and membrane-type-1-matrix-metaHoproteinase in endothelial cells and induction of vascular permeability in vivo by human inmunodeficiency virus-1 Tat protein and basic fibroblast growth factor. Mol Biol Cell,2001.12:2934—2946.
    [17]Brew K.Dinakarpandian D,Nagase H.Tissue inhibitors of metallproteinases evolution structure and function[J].Biochim 2000; 1477(1-2):267-283.
    [18]Taraboletti G,Ascenzo S,Borsotti G,Giavazzi R,Pavan A,Dolo V.Shedding of the matrix metalloproteinases MMP-2,MMP-9,and MTI-MMP as membrane vesi-cle-assiciated componets by endotheil cells(J).Am J Pathol,2002; 160(2):673-677.
    [19]Visse R, Nagase H. Matrix metalloproteinases and tissue inhibitors of metalloproteinases: structure,function,and biochemistry.Circ Res 2003;92(8):827-39
    [20]Ailawadi G, Eliason JL, Upchurch GR Jr. Current concepts in the pathogenesis of abdominal aortic aneurysm. J Vasc Surg 2003;38(3):584-8
    [21]Ailawadi G, Eliason JL, Roelofs KJ, et al. Gender differences in experimental aortic aneurysm formation. Arterioscler Thromb Vasc Biol 2004;24(11):2116-22
    [22]Wilson EM, Spinale FG. Myocardial remodelling and matrix metalloproteinases in heart failure:turmoil within the interstitium. Ann Med 2001;33(9):623-34
    [23]Faisal Aziz, Helena Kuivaniemi. Role of Matrix Metalloproteinase Inhibitors in Preventing Abdominal Aortic Aneurysm. Ann Vasc Surg.2007; 21(3):392-401
    [24]Mata KM, Prudente PS, Rocha FS,et al. Combining two potential causes of metallo-proteinase secretion causes abdominal aortic aneurysms in rats:a new experimental model, Int J Exp Pathol.2011;92(1):26-39
    [25]Aoki T, Kataoka H, Morimoto M,et al. Macrophage-derived matrix metalloproteinase-2 and-9 promote the progression of cerebral aneurysms in rats. Stroke.2007; 38:162-169.
    [26]齐巍,赵继宗,王硕,王嵘等;基质金属蛋白酶与脑囊性动脉瘤破裂的相关性研究.北京医学,2004;26(1):3-5
    [27]Pyo R, Lee JK, Shipley JM, et al. Targeted gene disruption of matrix metalloproteinase-9 (gelatinase-B) suppresses development of experimental abdominal aortic aneurysms. J Clin Invest 2000; 105(11):1641-9
    [28]Zhang L, Liao MF, Tian L,et al. Overexpression of interleukin-1βand interferon-γ in type Ⅰ thoracic aortic dissections and ascending thoracic aortic aneurysms:possible correlation with matrix metalloproteinase-9 expression and apoptosis of aortic media cells. Eur J Cardioth-orac Surg.2011;22 [Epub ahead of print]
    [29]Eskandari MK, Vijungco JD, Flores A, Borensztajn J, Shively V, Pearce WH. Enhanced abdominal aortic aneurysm in TIMP-1-deficient mice. J Surg Res.2005; 123:289-293
    [30]Ogata T, Shibamura H, Tromp G, Sinha M, Goddard KAB, Sakalihasan N, Limet R, MacKean GL, Arthur C, Sueda T, Land S, Kuivaniemi H. Genetic analysis of polymorp-hisms in biologically relevant candidate genes in patients with abdominal aortic aneurysms.J Vasc Surg.2005; 41:1036-1042
    [31]Ikonomidis JS, Gibson WC, Butler JE, McClister DM, Sweterlitsch SE, Thompson RP, Mukherjee R, Spinale FG. Effects of deletion of the tissue inhibitor of matrix metallop- roteinases-1 gene on the progression of murine thoracic aortic aneurysms. Circulation.2004; 110:Ⅱ268-Ⅱ273
    [32]Koullias GJ, Ravichandran P, Korkolis DP, Rimm DL, Elefteriades JA. Increased tissue microarray matrix metalloproteinase expression favors proteolysis in thoracic aortic aneurysms and dissections. Ann Thorac Surg.2004; 78:2106-2110
    [33]Eskandari MK, Vijungco JD, Flores A,et al. Enhanced abdominal aortic aneurysm in TIMP-1-deficient mice. J Surg Res.2005;123(2):289-93
    [34]Tomohiro Aoki,Hiroharu Kataoka,Takuya Moriwaki,et al. Role of TIMP-1 and TIMP-2 in the Progression of Cerebral Aneurysms. Stroke.2007;38:2337
    [1]赵继宗,万经海,马跃辉等,微创神经外科学:人民卫生出版社,2005:591-606
    [2]Dianshi Jin, Jun Sheng, Xinjian Yang, et.al. Matrix metalloproteinases and tissue inhibitors of metalloproteinases expression in human cerebral ruptured and unruptured aneurysm: Surgical Neurology,2007;68:11-17
    [3]International study of unruptured intracraniaaneurysms investigations. Unruptured intracranial aneurysms-risks of rupture and risks of surgical intervention. N Engl J Med, 1998,339(24):1725—1733.
    [4]Pfefferkorn T,Rosenberg GA,Closure of the blood-brain barrier by matrix metalloproteinase inhibition reduces rtPA-mediated mortality in cerebral ischemia with delayed reperfusion, Stroke,2003,34:63-68.
    [5]Pendas AM,Knauoer V,Puents XS,et al.Idenfication and characterization of a novel huaman matrix metaloproteinase with unique structural characteristic,chromosomal location,and tissue distibution[J].J Biol Chem,1997,272(7):4281-4286.
    [6]Creemers EE,Cleutjens JP,Smits JF,Daemen MJ.Matrix Metalloproteinase Inhibition After Myocardial Infarction A New Approach to Prevent Heart Failure?Circ Res,2001,89:201-210.
    [7]Masafumi K,Akihisa I.Role of matrix metalloproteinases in vascular remodeling. Journal of Atherosclerosis and Thrombosis,2003,10(5):275-282.25.
    [8]Toschi E, Barillari G. Sga dari C. et al. Activation of matrix-metlloproteinase-2 and membrane-type-l-matrix-metaHoproteinase in endothelial cells and induction of vascular permeability in vivo by human inmunodeficiency virus-1 Tat protein and basic fibroblast growth factor. Mol Biol Cell,2001.12:2934—2946.
    [9]Brew K,Dinakarpandian D,Nagase H.Tissue inhibitors of metallproteinases evolution, structure and function[J].Biochim 2000; 1477(1-2):267-283.
    [10]Taraboletti G,Ascenzo S,Borsotti G,Giavazzi R,Pavan A,Dolo V.Shedding of the matrix metal loproteinases MMP-2,MMP-9,and MTI-MMP as membrane vesi-cle-assiciated componets by endotheil cells(J).Am J Pathol,2002; 160(2):673-677.
    [11]Tomohiro Aoki, Hiroharu Kataoka, Takuya Moriwaki, et.al. Role of TIMP-I and TIMP-2 in the Progression of Cerebral Aneurysms:Stroke,2007;38:2337-2345
    [12]Pyo R,Lee J K,Shipley JM,et al. Targeted gene disruption of matrix metalloproteinase-9 (gelatinase B) suppresses development of experimental abdominal aortic aneurysms. J Clin Invest,2000,105:1641-1649.
    [13]Hong BK,Kwon HM,Lee BK,et al. Coexpression of cycolooxygenase-2 and matrix metalloproteinases in human aortic atherosclerotic lesions. Yonsei Med J,2000,41:82-88.
    [14]McGirt MJ,Lynch JR,Blessing R,et al.Serum von willebrand factor,matrix metalloproteinase-9 and vascular endothelial growth factor levels predict the onset of cerebral vasospasm after aneurismal subarachnoid hemorrhage. Neurosurgery,2002,51(5):1128-1134.
    [15]Tomohiro Aoki, Hiroharu Kataoka, Masafumi Morimoto,et.al. Macrophage-Derived Matrix Metalloproteinase-2 and-9 Promote the Progression of Cerebral Aneurysms in Rats: Stroke,2007;38:162-169
    [16]Gerard Tromp, Zoran Gatalica, Magdalena Skunca, et.al. Elevated Expression of Matrix Metalloproteinase-13 in Abdominal Aortic Aneurysms:Ann Vase Surg,2004; 18:414-420
    [17]Longo G,,Matthew B, Steven J. Buda, et.al. MMP-12 has a role in abdominal aortic aneurysms in mice:Surgery,2005; 137:457-62
    [18]Deguara J, Burnand KG, Taylor PR, et al. The 5A-allele of the matrix metalloproteinase-3 gene may be important in the pathogenesis of abdomifml aortic aneurysm formation[J]: British Journal of Surgery,2005,92(4),499-500.
    [19]Carrell T, Burnand K, Wells G, et al. Stromelysin-1 (matrix metalloproteinase-3)and tissue inhibitor of metalloproteinase-3 are overexpressed in the wall of abdominal aortic aneurysms[J]. Circulation,2002,105(4):477—82.
    [20]朱荣江,王任直,张波等;基质金属蛋白]酶-3在脑动脉瘤和脑外伤患者血清中的含量及意义;神经疾病与精神卫生;2005;5(1):4-5.
    [21]AAssar OS, Fujiwara NH, Marx WF, et al. Aneurysm growth, elastinolysis, and attempted doxycycline inhibition of elastase- induced aneurysms in rabbits [J]. J Vasc Interv Radiol,2003,14:1427-1432.
    [22]齐巍,赵继宗,王硕,王嵘等;基质金属蛋白酶与脑囊性动脉瘤破裂的相关性研究.北京医学,2004;26(1):3-5
    [23]Wilson WRW, Anderton M, Schwalbe EC, et al. Matrix metalloproteinase-8 and -9 are increased at the site of abdominal aortic aneurysm rupture:Circulation,2006;113:438-45
    [24]Baiping Zhang, Sahar Dhillon, Irene Geary, et.al. Polymorphisms in Matrix Metalloproteinase-1,-3,-9, and-12 Genes in Relation to Subarachnoid Hemorrhage:Stroke. 2001:32:2198-2202
    [25]Dietmar Krex, Henning Rohl, Inke R. Konig,et.al. Tissue Inhibitor of Metalloproteinases-1,-2, and -3 Polymorphisms in a White Population With Intracranial Aneurysms:Stroke,2003; 34:2817-2821
    [26]Xiaoju Wang, Gerard Tromp, C. William Cole, et.al. Analysis of coding sequences for tissue inhibitor of metalloproteinases 1 (TIMP1)and 2 (TIMP2)in patients with aneurysms:Matrix Biology,1999; 18:121-124
    [27]Irene Hinterseher, Dietmar Krex, Eberhard Kuhlisch,et.al. Tissue Inhibitor of Metalloproteinase-1 (TIMP-1) Polymorphisms in a Caucasian Population with Abdominal Aortic Aneurysm:World J Surg,2007;31:2248-2254

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