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 inChinese journal of traumatology Vol. 13; no. 5; pp. 308 - 312
Main Author 杨京 黄健 张耀宗 陈林
Format Journal Article
LanguageEnglish
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
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ISSN1008-1275
DOI10.3760/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.
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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Keywords Polymerase chain reaction
Sepsis
Ligation
Endothelial cells
Punctures
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Punctures
Sepsis
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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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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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https://dx.doi.org/10.3760/cma.j.issn.1008-1275.2010.05.011
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Volume 13
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