Expression profiling of laser-microdissected intrapulmonary arteries in hypoxia-induced pulmonary hypertension

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• 作者：Grazyna Kwapiszewska (1)
  Jochen Wilhelm (1)
  Stephanie Wolff (1)
  Isabel Laumanns (1)
  Inke R Koenig (2)
  Andreas Ziegler (2)
  Werner Seeger (3)
  Rainer M Bohle (1)
  Norbert Weissmann (3)
  Ludger Fink (1)
  
• 刊名：Respiratory Research
• 出版年：2005
• 出版时间：December 2005
• 年：2005
• 卷：6
• 期：1
• 全文大小：2051KB
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• 作者单位：Grazyna Kwapiszewska (1)
  Jochen Wilhelm (1)
  Stephanie Wolff (1)
  Isabel Laumanns (1)
  Inke R Koenig (2)
  Andreas Ziegler (2)
  Werner Seeger (3)
  Rainer M Bohle (1)
  Norbert Weissmann (3)
  Ludger Fink (1)
  
  1. Department of Pathology, Justus-Liebig-University Giessen, Germany
  2. Department of Medical Biometry and Statistics, University at Luebeck, Germany
  3. Department of Internal Medicine, Justus-Liebig-University Giessen, Germany
  

文摘

Background Chronic hypoxia influences gene expression in the lung resulting in pulmonary hypertension and vascular remodelling. For specific investigation of the vascular compartment, laser-microdissection of intrapulmonary arteries was combined with array profiling. Methods and Results Analysis was performed on mice subjected to 1, 7 and 21 days of hypoxia (FiO2 = 0.1) using nylon filters (1176 spots). Changes in the expression of 29, 38, and 42 genes were observed at day 1, 7, and 21, respectively. Genes were grouped into 5 different classes based on their time course of response. Gene regulation obtained by array analysis was confirmed by real-time PCR. Additionally, the expression of the growth mediators PDGF-B, TGF-β, TSP-1, SRF, FGF-2, TIE-2 receptor, and VEGF-R1 were determined by real-time PCR. At day 1, transcription modulators and ion-related proteins were predominantly regulated. However, at day 7 and 21 differential expression of matrix producing and degrading genes was observed, indicating ongoing structural alterations. Among the 21 genes upregulated at day 1, 15 genes were identified carrying potential hypoxia response elements (HREs) for hypoxia-induced transcription factors. Three differentially expressed genes (S100A4, CD36 and FKBP1a) were examined by immunohistochemistry confirming the regulation on protein level. While FKBP1a was restricted to the vessel adventitia, S100A4 and CD36 were localised in the vascular tunica media. Conclusion Laser-microdissection and array profiling has revealed several new genes involved in lung vascular remodelling in response to hypoxia. Immunohistochemistry confirmed regulation of three proteins and specified their localisation in vascular smooth muscle cells and fibroblasts indicating involvement of different cells types in the remodelling process. The approach allows deeper insight into hypoxic regulatory pathways specifically in the vascular compartment of this complex organ.