Tie2 mRNA in peripheral blood: a new marker to assess damage of endothelial cells in a rat model of sepsis
Objective: To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis. Methods: The model of sepsis was established by cecal ligation and puncture (CLP) in 90 rats which were divided into 6 groups: normal, sham, CLP-3 h, CLP-6 h, CLP- 12 h and CLP-2...
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Published in | Chinese journal of traumatology Vol. 13; no. 5; pp. 308 - 312 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
China
Elsevier B.V
01.10.2010
State Key Laboratory of Trauma, Burns and Combined Injury, Trauma Center, Trauma Laboratory, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing 400042, China%Intensive Care Unit, Institute of Surgery Research,Daping Hospital, Third Military Medical University,Chongqing 400042, China |
Subjects | |
Online Access | Get full text |
ISSN | 1008-1275 |
DOI | 10.3760/cma.j.issn.1008-1275.2010.05.011 |
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Abstract | Objective: To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis. Methods: The model of sepsis was established by cecal ligation and puncture (CLP) in 90 rats which were divided into 6 groups: normal, sham, CLP-3 h, CLP-6 h, CLP- 12 h and CLP-24 h. Serum biochemical markers were detected by automatic biochemical analyzer. Serum IL-6 was measured with enzyme linked immunosorbent assay. The vascular permeability of liver, kidney, lung and heart was detected with Evans blue. Circulating endothelial cells (CEC) were separated using density gradient separation and counted. Total RNA of whole blood were extracted and the mRNA levels of two endothelial specific genes, Tie2 and vascular endothelial growth factor receptor 2 (VEGFR2), were measured by quantitative real-time PCR. Results: The level of serum biochemical indexes increased after CLP. The amount of serum IL-6 in CLP-6 h, 12 h,and 24 h group was increased 6.5-fold (P〈 0.05), 8.4-fold (P〈 0.01 ), and 13.3-fold (P〈0.001 ) compared with normal group ( 170.68 pg/mli42.46 pg/ml) respectively (F= 14.319, P〈0.001). Significantly increased organ vasopermeability of liver, kidney, lung and heart was observed after CLP respectively. The number of CEC peaked (11.83±1.94) 3 hours after CLP compared with normal control (5.33±1.21, P〈0.05), and then decreased gradually (F=54.183, P〈0.001). The mRNA level of Tie2 in CLP-3 h group (3.47±1.47) was also markedly higher than that in other groups (F=10.640, P〈0.001 ). Conclusion: Using quantitative real-time PCR to measure the level of Tie2 mRNA in peripheral blood is a simple and relatively sensitive method to evaluate the damage of endothelial cells. |
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AbstractList | To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis.
The model of sepsis was established by cecal ligation and puncture (CLP) in 90 rats which were divided into 6 groups: normal, sham, CLP-3 h, CLP-6 h, CLP-12 h and CLP-24 h. Serum biochemical markers were detected by automatic biochemical analyzer. Serum IL-6 was measured with enzyme linked immunosorbent assay. The vascular permeability of liver, kidney, lung and heart was detected with Evans blue. Circulating endothelial cells (CEC) were separated using density gradient separation and counted. Total RNA of whole blood were extracted and the mRNA levels of two endothelial specific genes, Tie2 and vascular endothelial growth factor receptor 2 (VEGFR 2), were measured by quantitative real-time PCR.
The level of serum biochemical indexes increase d after CLP. The amount of s erum IL-6 in C LP-6 h, 12 h, and 24 h group was increased 6.5-fold (
P<0.05), 8.4-fold (
P<0.01), and 13.3-fold (
P<0.001) compared with normal group (170.68 pg/ml±42.46 pg/ml) respectively (
F=14.319,
P<0.001). Significantly increased organ vasopermeability of liver, kidney, lung and heart was observed after CLP respectively. The number of CEC peaked (11.83±1.94) 3 hours after CLP compared with normal control (5.33±1.21,
P<0.05), and then decreased gradually (
F=54.183,
P<0.001). The mRNA level of Tie2 in CLP-3 h group (3.47±1.47) was also markedly higher than that in other groups (
F=10.640,
P<0.001).
Using quantitative real-time PCR to measure the level of Tie2 mRNA in peripheral blood is a simple and relatively sensitive method to evaluate the damage of endothelial cells. R6; Objective: To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis.Methods: The model of sepsis was established by cecal ligation and puncture (CLP) in 90 rats which were divided into 6 groups: normal, sham, CLP-3 h, CLP-6 h, CLP12 h and CLP-24 h. Serum biochemical markers were detected by automatic biochemical analyzer. Serum IL-6 was measured with enzyme linked immunosorbent assay. The vascular permeability of liver, kidney, lung and heart was detected with Evans blue. Circulating endothelial cells (CEC)were separated using density gradient separation and counted. Total RNA of whole blood were extracted and the mRNA levels of two endothelial specific genes, Tie2 and vascular endothelial growth factor receptor 2 (VEGFR2), were measured by quantitative real-time PCR.Results: The level of serum biochemical indexes increased after CLP. The amount of serum IL-6 in CLP-6 h, 12 h,and 24 h group was increased 6.5-fold (P<0.05), 8.4-fold (P<0.01 ), and 13.3-fold (P<0.001 ) compared with normal group ( 170.68 pg/ml±42.46 pg/ml) respectively (F=14.319,P<0.001). Significantly increased organ vasopermeabilityof liver, kidney, lung and heart was observed after CLPrespectively. The number of CEC peaked (11.83± 1.94) 3hours after CLP compared with normal control (5.33± 1.21,P<0.05), and then decreased gradually (F=54.183, P<0.001).The mRNA level of Tie2 in CLP-3 h group (3.47±1.47) was also markedly higher than that in other groups (F=10.640,P<0.001).Conclusion: Using quantitative real-time PCR to measure the level of Tie2 mRNA in peripheral blood is a simple and relatively sensitive method to evaluate the damage of endothelial cells. Objective: To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis. Methods: The model of sepsis was established by cecal ligation and puncture (CLP) in 90 rats which were divided into 6 groups: normal, sham, CLP-3 h, CLP-6 h, CLP- 12 h and CLP-24 h. Serum biochemical markers were detected by automatic biochemical analyzer. Serum IL-6 was measured with enzyme linked immunosorbent assay. The vascular permeability of liver, kidney, lung and heart was detected with Evans blue. Circulating endothelial cells (CEC) were separated using density gradient separation and counted. Total RNA of whole blood were extracted and the mRNA levels of two endothelial specific genes, Tie2 and vascular endothelial growth factor receptor 2 (VEGFR2), were measured by quantitative real-time PCR. Results: The level of serum biochemical indexes increased after CLP. The amount of serum IL-6 in CLP-6 h, 12 h,and 24 h group was increased 6.5-fold (P〈 0.05), 8.4-fold (P〈 0.01 ), and 13.3-fold (P〈0.001 ) compared with normal group ( 170.68 pg/mli42.46 pg/ml) respectively (F= 14.319, P〈0.001). Significantly increased organ vasopermeability of liver, kidney, lung and heart was observed after CLP respectively. The number of CEC peaked (11.83±1.94) 3 hours after CLP compared with normal control (5.33±1.21, P〈0.05), and then decreased gradually (F=54.183, P〈0.001). The mRNA level of Tie2 in CLP-3 h group (3.47±1.47) was also markedly higher than that in other groups (F=10.640, P〈0.001 ). Conclusion: Using quantitative real-time PCR to measure the level of Tie2 mRNA in peripheral blood is a simple and relatively sensitive method to evaluate the damage of endothelial cells. To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis.OBJECTIVETo evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis.The model of sepsis was established by cecal ligation and puncture (CLP) in 90 rats which were divided into 6 groups: normal, sham, CLP-3 h, CLP-6 h, CLP-12 h and CLP-24 h. Serum biochemical markers were detected by automatic biochemical analyzer. Serum IL-6 was measured with enzyme linked immunosorbent assay. The vascular permeability of liver, kidney, lung and heart was detected with Evans blue. Circulating endothelial cells (CEC) were separated using density gradient separation and counted. Total RNA of whole blood were extracted and the mRNA levels of two endothelial specific genes, Tie2 and vascular endothelial growth factor receptor 2 (VEGFR2), were measured by quantitative real-time PCR.METHODSThe model of sepsis was established by cecal ligation and puncture (CLP) in 90 rats which were divided into 6 groups: normal, sham, CLP-3 h, CLP-6 h, CLP-12 h and CLP-24 h. Serum biochemical markers were detected by automatic biochemical analyzer. Serum IL-6 was measured with enzyme linked immunosorbent assay. The vascular permeability of liver, kidney, lung and heart was detected with Evans blue. Circulating endothelial cells (CEC) were separated using density gradient separation and counted. Total RNA of whole blood were extracted and the mRNA levels of two endothelial specific genes, Tie2 and vascular endothelial growth factor receptor 2 (VEGFR2), were measured by quantitative real-time PCR.The level of serum biochemical indexes increased after CLP. The amount of serum IL-6 in CLP-6 h, 12 h, and 24 h group was increased 6.5-fold (P <0.05), 8.4-fold (P < 0.01), and 13.3-fold (P < 0.001) compared with normal group (170.68 pg/ml ± 42.46 pg/ml) respectively (F = 14.319, P < 0.001). Significantly increased organ vasopermeability of liver, kidney, lung and heart was observed after CLP respectively. The number of CEC peaked (11.83 ± 1.94) 3 hours after CLP compared with normal control (5.33 ± 1.21, P < 0.05), and then decreased gradually (F = 54.183, P < 0.001). The mRNA level of Tie2 in CLP-3 h group (3.47 ± 1.47) was also markedly higher than that in other groups (F = 10.640, P < 0.001).RESULTSThe level of serum biochemical indexes increased after CLP. The amount of serum IL-6 in CLP-6 h, 12 h, and 24 h group was increased 6.5-fold (P <0.05), 8.4-fold (P < 0.01), and 13.3-fold (P < 0.001) compared with normal group (170.68 pg/ml ± 42.46 pg/ml) respectively (F = 14.319, P < 0.001). Significantly increased organ vasopermeability of liver, kidney, lung and heart was observed after CLP respectively. The number of CEC peaked (11.83 ± 1.94) 3 hours after CLP compared with normal control (5.33 ± 1.21, P < 0.05), and then decreased gradually (F = 54.183, P < 0.001). The mRNA level of Tie2 in CLP-3 h group (3.47 ± 1.47) was also markedly higher than that in other groups (F = 10.640, P < 0.001).Using quantitative real-time PCR to measure the level of Tie2 mRNA in peripheral blood is a simple and relatively sensitive method to evaluate the damage of endothelial cells.CONCLUSIONUsing quantitative real-time PCR to measure the level of Tie2 mRNA in peripheral blood is a simple and relatively sensitive method to evaluate the damage of endothelial cells. To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis. The model of sepsis was established by cecal ligation and puncture (CLP) in 90 rats which were divided into 6 groups: normal, sham, CLP-3 h, CLP-6 h, CLP-12 h and CLP-24 h. Serum biochemical markers were detected by automatic biochemical analyzer. Serum IL-6 was measured with enzyme linked immunosorbent assay. The vascular permeability of liver, kidney, lung and heart was detected with Evans blue. Circulating endothelial cells (CEC) were separated using density gradient separation and counted. Total RNA of whole blood were extracted and the mRNA levels of two endothelial specific genes, Tie2 and vascular endothelial growth factor receptor 2 (VEGFR2), were measured by quantitative real-time PCR. The level of serum biochemical indexes increased after CLP. The amount of serum IL-6 in CLP-6 h, 12 h, and 24 h group was increased 6.5-fold (P <0.05), 8.4-fold (P < 0.01), and 13.3-fold (P < 0.001) compared with normal group (170.68 pg/ml ± 42.46 pg/ml) respectively (F = 14.319, P < 0.001). Significantly increased organ vasopermeability of liver, kidney, lung and heart was observed after CLP respectively. The number of CEC peaked (11.83 ± 1.94) 3 hours after CLP compared with normal control (5.33 ± 1.21, P < 0.05), and then decreased gradually (F = 54.183, P < 0.001). The mRNA level of Tie2 in CLP-3 h group (3.47 ± 1.47) was also markedly higher than that in other groups (F = 10.640, P < 0.001). Using quantitative real-time PCR to measure the level of Tie2 mRNA in peripheral blood is a simple and relatively sensitive method to evaluate the damage of endothelial cells. |
Author | 杨京 黄健 张耀宗 陈林 |
AuthorAffiliation | State Key Laboratory of Trauma, Burns and Combined Injury, Trauma Center, Trauma Laboratory, Institute of Sur- gery Research, Daping Hospital, Third Military Medical University. Chonaaina 400042, China Intensive Care Unit, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing 400042, China |
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Publisher | Elsevier B.V State Key Laboratory of Trauma, Burns and Combined Injury, Trauma Center, Trauma Laboratory, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing 400042, China%Intensive Care Unit, Institute of Surgery Research,Daping Hospital, Third Military Medical University,Chongqing 400042, China |
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References | Rajagopalan, Somers, Brook (bib260) 2004; 103 Rabascio, Muratori, Mancuso (bib170) 2004; 64 Erdbruegger, Haubitz, Woywodt (bib60) 2006; 373 Johansson, Rudolfsson, Wikström (bib80) 2005; 146 Steinle, Lashbrook (bib90) 2006; 83 Remick, Newcomb, Bolgos (bib120) 2000; 13 Boehme, Galle, Stremmel (bib160) 2002; 107 Cho, Sung, Kim (bib200) 2006; 103 Rafat, Hanusch, Brinkkoetter (bib40) 2007; 35 Usui, Kuriyama, Kisawada (bib230) 2009; 16 Schouten, Wiersinga, Levi (bib30) 2008; 83 Annane, Bellissant, Cavaillon (bib10) 2005; 365 Singleton, Wischmeyer (bib130) 2003; 35 Furstenberger, von Moos, Senn (bib70) 2005; 93 Harhaj, Antonetti (bib220) 2004; 36 Ruegg, Dormond, Foletti (bib150) 2002; 9 Rundle, Wang, Yu (bib100) 2006; 38 Kluz, Kopec, Jakobsche-Policht (bib250) 2009; 28 Nykänen, Krebs, Saaristo (bib210) 2003; 107 Loughna, Sato (bib180) 2001; 20 Henneke, Golenbock (bib20) 2002; 30 Yancopoulos, Davis, Gale (bib190) 2000; 407 Megarbane, Marchal, Marfaing-Koka (bib50) 2004; 30 Dignat-George, Sampol (bib240) 2000; 65 Franco, de Jonge, Dekkers (bib140) 2000; 96 Rittirsch, Hoesel, Ward (bib110) 2007; 81 |
References_xml | – volume: 36 start-page: 1206 year: 2004 end-page: 1237 ident: bib220 article-title: Regulation of tight junctions and loss of barrier function in pathophysiology publication-title: Int J Biochem Cell Biol – volume: 83 start-page: 536 year: 2008 end-page: 545 ident: bib30 article-title: Inflammation, endothelium, and coagulation in sepsis publication-title: J Leukoc Biol – volume: 28 start-page: 192 year: 2009 end-page: 201 ident: bib250 article-title: Circulating endothelial cells, endothelial apoptosis and soluble markers of endothelial dysfunction in patients with systemic lupus erythe-matosus-related vasculitis publication-title: Int Angiol – volume: 107 start-page: 1308 year: 2003 end-page: 1314 ident: bib210 article-title: Angiopoietin-1 protects against the development of cardiac allograft arteriosclerosis publication-title: Circulation – volume: 35 start-page: 1677 year: 2007 end-page: 1684 ident: bib40 article-title: Increased circulating endothelial progenitor cells in septic patients: correlation with survival publication-title: Crit Care Med – volume: 65 start-page: 215 year: 2000 end-page: 220 ident: bib240 article-title: Circulating endothelial cells in vascular disorders: new insights into an old concept publication-title: Eur J Haematol – volume: 365 start-page: 63 year: 2005 end-page: 78 ident: bib10 article-title: Septic shock publication-title: Lancet – volume: 373 start-page: 17 year: 2006 end-page: 26 ident: bib60 article-title: Circulating en-dothelial cells: a novel marker of endothelial damage publication-title: Clin Chim Acta – volume: 83 start-page: 16 year: 2006 end-page: 23 ident: bib90 article-title: Cervical sympathectomy regulates expression of key angiogenic factors in the rat choroid publication-title: Exp Eye Res – volume: 96 start-page: 554 year: 2000 end-page: 559 ident: bib140 article-title: The in vivo kinetics of tissue factor messenger RNA expression during human endotoxemia: relationgship with activation of coagulation publication-title: Blood – volume: 30 start-page: S207 year: 2002 end-page: S213 ident: bib20 article-title: Innate immune recognition of lipopolysaccharide by endothelial cells publication-title: Crit Care Med – volume: 64 start-page: 4373 year: 2004 end-page: 4377 ident: bib170 article-title: Assessing tumor angiogenesis: increased circulating VE-cadherin RNA in patients with cancer indicates viability of circulating endothelial cells publication-title: Cancer Res – volume: 20 start-page: 319 year: 2001 end-page: 325 ident: bib180 article-title: Angiopoietin and Tie signaling pathways in vascular development publication-title: Matrix Biol – volume: 81 start-page: 1 year: 2007 end-page: 7 ident: bib110 article-title: The disconnect between animal models of sepsis and human sepsis publication-title: J Leukocyte Biol – volume: 38 start-page: 521 year: 2006 end-page: 529 ident: bib100 article-title: Microarray analysis of gene expression during the inflammation and endochondral bone formation stages of rat femur fracture repair publication-title: Bone – volume: 16 start-page: 513 year: 2009 end-page: 520 ident: bib230 article-title: Tissue factor expression demonstrates severe sinusoidal endothelial cell damage during rejection after living-donor liver transplantation publication-title: J Hepatobiliary Pancreat Surg – volume: 30 start-page: 867 year: 2004 end-page: 874 ident: bib50 article-title: Increased diffusion of soluble adhesion molecules in meningitis, severe sepsis and systemic inflammatory response without neurological infection is associated with intrathecal shedding in cases of meningitis publication-title: Intensive Care Med – volume: 13 start-page: 110 year: 2000 end-page: 116 ident: bib120 article-title: Comparison of the mortality and inflammatory response of two models of sepsis: lipopolysaccharide vs. cecal ligation and puncture publication-title: Shock – volume: 407 start-page: 242 year: 2000 end-page: 248 ident: bib190 article-title: Vascular-specific growth factors and blood vessel formation publication-title: Nature – volume: 146 start-page: 3463 year: 2005 end-page: 3470 ident: bib80 article-title: Altered levels of angiopoietin 1 and tie 2 are associated with androgen-regulated vascular regression and growth in the ventral prostate in adult mice and rats publication-title: Endocrinology – volume: 103 start-page: 4946 year: 2006 end-page: 4951 ident: bib200 article-title: COMP-angiopoietin-1 promotes wound healing through enhanced angiogenesis, lymphangiogenesis, and blood flow in a diabetic mouse model publication-title: Proc Natl Acad Sci USA – volume: 103 start-page: 3677 year: 2004 end-page: 3683 ident: bib260 article-title: Endothelial cell apoptosis in systemic lupus erythematosus: a common pathway for abnormal vascular function and thrombosis propensity publication-title: Blood – volume: 9 start-page: 151 year: 2002 end-page: 160 ident: bib150 article-title: Suppression of tumor angiogenesis through the inhibition of integrin function and signaling in endothelial cells: which side to target? publication-title: Endothelium – volume: 93 start-page: 793 year: 2005 end-page: 798 ident: bib70 article-title: Real-time PCR of CD146 mRNA in peripheral blood enables the relative quantification of circulating endothelial cells and is an indicator of angiogenesis publication-title: Br J Cancer – volume: 35 start-page: 486 year: 2003 end-page: 491 ident: bib130 article-title: Distance of cecum ligated influences mortality, tumor necrosis factor-alpha and interleukin-6 expression following cecal ligation and puncture in the rat publication-title: Eur Surg Res – volume: 107 start-page: 340 year: 2002 end-page: 349 ident: bib160 article-title: Kinetics of thrombomodulin release and endothelial cell injury by neutrophil-derived proteases and oxygen radicals publication-title: Immunology |
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Snippet | Objective: To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis. Methods: The model of sepsis was... To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis. The model of sepsis was established by cecal... To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis.OBJECTIVETo evaluate the endothelial cell damage... R6; Objective: To evaluate the endothelial cell damage by detecting the circulating Tie2 mRNA level in a rat model of sepsis.Methods: The model of sepsis was... |
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SubjectTerms | Animals Biomarkers - blood Capillary Permeability Endothelial cells Endothelial Cells - pathology Interleukin-6 - blood Ligation Male mRNA水平 Polymerase chain reaction Punctures Rats Rats, Sprague-Dawley Receptor, TIE-2 - genetics RNA, Messenger - blood Sepsis Sepsis - pathology 外周血 大鼠模型 细胞损伤 脓毒症 血管内皮生长因子受体 |
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Title | Tie2 mRNA in peripheral blood: a new marker to assess damage of endothelial cells in a rat model of sepsis |
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