Delineating the angiogenic gene expression profile before pulmonary vascular remodeling in a lamb model of congenital heart disease

Jing Tian, Sohrab Fratz, Yali Hou, Qing Lu, Agnes Görlach, John Hess, Christian Schreiber, Sanjeev A. Datar, Peter Oishi, John Nechtman, Robert Podolsky, Jin-Xiong She, Jeffrey R. Fineman, Stephen Matthew Black

Research output: Contribution to journalArticle

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Abstract

Disordered angiogenesis is implicated in pulmonary vascular remodeling secondary to congenital heart diseases (CHD). However, the underlying genes are not well delineated. We showed previously that an ovine model of CHD with increased pulmonary blood flow (PBF, Shunt) has an "angiogenesis burst" between 1 and 4 wk of age. Thus we hypothesized that the increased PBF elicited a proangiogenic gene expression profile before onset of vessel growth. To test this we utilized microarray analysis to identify genes that could be responsible for the angiogenic response. Total RNA was isolated from lungs of Shunt and control lambs at 3 days of age and hybridized to Affymetrix gene chips for microarray analyses (n = 8/group). Eighty-nine angiogenesis-related genes were found to be upregulated and 26 angiogenesis-related genes downregulated in Shunt compared with control lungs (cutting at 1.2-fold difference, P < 0.05). We then confirmed upregulation of proangiogenic genes FGF2, Angiopoietin2 (Angpt2), and Birc5 at mRNA and protein levels and upregulation of ccl2 at mRNA level in 3-day Shunt lungs. Furthermore, we found that pulmonary arterial endothelial cells (PAEC) isolated from fetal lambs exhibited increased expression of FGF2, Angpt2, Birc5, and ccl2 and enhanced angiogenesis when exposed to elevated shear stress (35 dyn/cm 2) compared with cells exposed to more physiological shear stress (20 dyn/cm2). Finally, we demonstrated that blocking FGF2, Angpt2, Birc5, or ccl2 signaling with neutralizing antibodies or small interfering RNA (siRNA) significantly decreased the angiogenic response induced by shear stress. In conclusion, we have identified a "proangiogenic" gene expression profile in a lamb model of CHD with increased PBF that precedes onset of pulmonary vascular remodeling. Our data indicate that FGF2, Angpt2, Birc5, and ccl2 may play important roles in the angiogenic response.

Original languageEnglish (US)
Pages (from-to)87-98
Number of pages12
JournalPhysiological Genomics
Volume43
Issue number2
DOIs
StatePublished - Jan 1 2011

Fingerprint

Transcriptome
Heart Diseases
Lung
Fibroblast Growth Factor 2
Genes
Microarray Analysis
Up-Regulation
Messenger RNA
Vascular Remodeling
Neutralizing Antibodies
Oligonucleotide Array Sequence Analysis
Small Interfering RNA
Sheep
Down-Regulation
Endothelial Cells
RNA
Growth
Proteins

Keywords

  • Microarray
  • Pulmonary hypertension
  • Shear stress

ASJC Scopus subject areas

  • Physiology
  • Genetics

Cite this

Delineating the angiogenic gene expression profile before pulmonary vascular remodeling in a lamb model of congenital heart disease. / Tian, Jing; Fratz, Sohrab; Hou, Yali; Lu, Qing; Görlach, Agnes; Hess, John; Schreiber, Christian; Datar, Sanjeev A.; Oishi, Peter; Nechtman, John; Podolsky, Robert; She, Jin-Xiong; Fineman, Jeffrey R.; Black, Stephen Matthew.

In: Physiological Genomics, Vol. 43, No. 2, 01.01.2011, p. 87-98.

Research output: Contribution to journalArticle

Tian, J, Fratz, S, Hou, Y, Lu, Q, Görlach, A, Hess, J, Schreiber, C, Datar, SA, Oishi, P, Nechtman, J, Podolsky, R, She, J-X, Fineman, JR & Black, SM 2011, 'Delineating the angiogenic gene expression profile before pulmonary vascular remodeling in a lamb model of congenital heart disease', Physiological Genomics, vol. 43, no. 2, pp. 87-98. https://doi.org/10.1152/physiolgenomics.00135.2010
Tian, Jing ; Fratz, Sohrab ; Hou, Yali ; Lu, Qing ; Görlach, Agnes ; Hess, John ; Schreiber, Christian ; Datar, Sanjeev A. ; Oishi, Peter ; Nechtman, John ; Podolsky, Robert ; She, Jin-Xiong ; Fineman, Jeffrey R. ; Black, Stephen Matthew. / Delineating the angiogenic gene expression profile before pulmonary vascular remodeling in a lamb model of congenital heart disease. In: Physiological Genomics. 2011 ; Vol. 43, No. 2. pp. 87-98.
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