Display options
Share it on

Exp Transl Stroke Med. 2011 Oct 26;3:12. doi: 10.1186/2040-7378-3-12.

The ATP-binding cassette transporters ABCB1 and ABCC1 are not regulated by hypoxia in immortalised human brain microvascular endothelial cells.

Experimental & translational stroke medicine

Pauline Patak, Fengyan Jin, Simon T Schäfer, Eric Metzen, Dirk M Hermann

Affiliations

  1. Department of Neurology, University Hospital Essen, Germany. [email protected].

PMID: 22029974 PMCID: PMC3213079 DOI: 10.1186/2040-7378-3-12

Abstract

BACKGROUND: ATP-binding cassette transporters at the blood-brain barrier are actively regulated upon ischemic stroke in a way that impedes the access of pharmacological compounds to the brain tissue. The luminal endothelial transporter ABCB1 was recently shown to be increased, whereas the abluminal transporter ABCC1 was decreased on ischemic brain capillaries. In vitro studies using epithelial cells suggested that ABCB1 is regulated during hypoxia in a hypoxia-inducible factor (HIF)-1α-dependent way.

METHODS: In order to investigate whether hypoxia might be responsible for the expression changes of ABCB1 and ABCC1 in the ischemic brain, the immortalised human brain microvascular endothelial cell line hCMEC/D3 was exposed to hypoxia (1%) or anoxia (0%). Cell lysates were analysed by Western blot to detect the protein expression of ABCB1, ABCC1, HIF-1α and HIF-2α.

RESULTS: During hypoxia, an accumulation of HIF-1α and HIF-2α was noticed in hCMEC/D3 cells that followed different time kinetics. Both HIF-1α and HIF-2α abundance increased within 4 h of hypoxia. HIF-1α levels decreased to below detection levels within 16 h of hypoxia, whereas HIF-2α remained elevated even after 48 h. No changes of ABCB1 and ABCC1 expression were detected, neither on the mRNA nor protein level.

CONCLUSION: Our data suggests that other factors than hypoxia may be responsible for the expression changes of ATP-binding cassette transporters in the ischemic brain.

References

  1. Sci Signal. 2010 Oct 05;3(142):ra72 - PubMed
  2. FASEB J. 2005 Nov;19(13):1872-4 - PubMed
  3. Brain. 2008 Oct;131(Pt 10):2679-89 - PubMed
  4. Adv Exp Med Biol. 2008;614:157-64 - PubMed
  5. Cancer Res. 2002 Jun 15;62(12):3387-94 - PubMed
  6. J Neurochem. 2002 Jan;80(1):64-72 - PubMed
  7. Ann Neurol. 2006 Nov;60(5):489-98 - PubMed
  8. J Neurochem. 2009 Oct;111(1):132-41 - PubMed
  9. Neurosci Lett. 2008 Feb 27;432(3):184-7 - PubMed
  10. Mol Cell Biol. 2003 Dec;23(24):9361-74 - PubMed
  11. Nat Rev Neurosci. 2006 Jan;7(1):41-53 - PubMed
  12. NeuroRx. 2005 Jan;2(1):86-98 - PubMed
  13. Nat Neurosci. 2006 Apr;9(4):487-8 - PubMed
  14. Cancer Res. 2003 Nov 1;63(21):7284-90 - PubMed

Publication Types