Analysis of TGF-beta 1 gene expression in contused rat spinal cord using quantitative RT-PCR

被引:53
|
作者
SempleRowland, SL [1 ]
Mahatme, A [1 ]
Popovich, PG [1 ]
Green, DA [1 ]
Hassler, G [1 ]
Stokes, BT [1 ]
Streit, WJ [1 ]
机构
[1] OHIO STATE UNIV, COLL MED, SPINAL CORD INJURY RES CTR, DEPT PHYSIOL, COLUMBUS, OH 43210 USA
关键词
cytokine; cyclophilin; inflammation; reactive gliosis; regeneration; spinal cord injury; transforming growth factor beta;
D O I
10.1089/neu.1995.12.1003
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
We have used northern blot analysis and quantitative reverse transcription polymerase chain reaction (RT-PCR) to determine the postinjury expression profile of the transforming growth factor-beta 1 (TGF-beta 1) gene in the contused rat spinal cord, Spectrophotometric estimates of total sample RNA and quantitative analyses of cyclophilin mRNA using RT-PCR served as controls for comparisons between samples, No changes in cyclophilin gene expression were found at any postinjury survival times, The results of the TGF-beta 1 analyses, which were carried out on spinal cord samples taken at postinjury intervals ranging from 6 h to 10 days, show that the amount of TGF-beta 1 mRNA present in spinal cord increases rapidly following injury, reaching maximum levels 7 days postinjury. Unoperated control samples contained approximately 2 x 10(8) molecules of TGF-beta 1 mRNA/0.5 mu g total RNA. By 1 day postinjury, the amount of TGF-beta 1 mRNA in the cord had increased by a factor of 2.5 to 5 x 10(8) molecules/0.5 mu g total RNA, At 7 days postinjury, there were approximately 15 x 10(8) molecules of TGF-beta 1 mRNA/0.5 mu g total RNA. By 10 days postinjury the amount of TGF-beta 1 mRNA present in the spinal cord had declined to 8 x 10(8) molecules of TGF-beta 1 mRNA/0.5 mu g total RNA, a value similar to that observed at 3 days postinjury, The roles that TGF-beta 1 might play in modifying cellular responses in injured spinal cord are discussed.
引用
收藏
页码:1003 / 1014
页数:12
相关论文
共 50 条
  • [1] ONTOGENY OF TGF-BETA(1) AND AT(1) GENE-EXPRESSION IN THE RAT
    TUFROMCREDDIE, A
    EVERETT, AD
    GOMEZ, RA
    PEDIATRIC RESEARCH, 1994, 35 (04) : A375 - A375
  • [2] QUANTITATIVE RT-PCR FOR MEASURING GENE-EXPRESSION
    RIEDY, MC
    TIMM, EA
    STEWART, CC
    BIOTECHNIQUES, 1995, 18 (01) : 70 - &
  • [3] Spatial and temporal gene expression profiling of the contused rat spinal cord
    Aimone, JB
    Leasure, JL
    Perreau, VM
    Thallmair, M
    EXPERIMENTAL NEUROLOGY, 2004, 189 (02) : 204 - 221
  • [4] Evaluation of Reference Genes for Gene Expression Analysis Using Quantitative RT-PCR in Azospirillum brasilense
    McMillan, Mary
    Pereg, Lily
    PLOS ONE, 2014, 9 (05):
  • [5] Investigation of Reference Genes in Vibrio parahaemolyticus for Gene Expression Analysis Using Quantitative RT-PCR
    Ma, Yue-jiao
    Sun, Xiao-hong
    Xu, Xiao-yan
    Zhao, Yong
    Pan, Ying-jie
    Hwang, Cheng-An
    Wu, Vivian C. H.
    PLOS ONE, 2015, 10 (12):
  • [6] Gene expression of trisomy 21 placenta using expression microarrays and quantitative RT-PCR
    Jonish, A
    Bar-Shira, A
    Ochshorn, Y
    Rozovzki, U
    Goldstein, M
    Yaron, Y
    AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2005, 193 (06) : S163 - S163
  • [7] Quantitative analysis of NQO1 gene expression by RT-PCR and CE-LIF
    Kolesar, JM
    Rizzo, JD
    Kuhn, JG
    JOURNAL OF CAPILLARY ELECTROPHORESIS, 1995, 2 (06) : 287 - 290
  • [8] Quantitative RT-PCR gene expression analysis of laser microdissected tissue samples
    Heidi S Erickson
    Paul S Albert
    John W Gillespie
    Jaime Rodriguez-Canales
    W Marston Linehan
    Peter A Pinto
    Rodrigo F Chuaqui
    Michael R Emmert-Buck
    Nature Protocols, 2009, 4 : 902 - 922
  • [9] Quantitative RT-PCR gene expression analysis of laser microdissected tissue samples
    Erickson, Heidi S.
    Albert, Paul S.
    Gillespie, John W.
    Rodriguez-Canales, Jaime
    Linehan, W. Marston
    Pinto, Peter A.
    Chuaqui, Rodrigo F.
    Emmert-Buck, Michael R.
    NATURE PROTOCOLS, 2009, 4 (06) : 902 - 922
  • [10] A method for the quantitative analysis of human heat shock gene expression using a multiplex RT-PCR assay
    Wang, SM
    Khandekar, JD
    Kaul, KL
    Winchester, DJ
    Morimoto, RI
    CELL STRESS & CHAPERONES, 1999, 4 (03): : 153 - 161