mRna expression and transport characterization of conditionally immortalized rat brain capillary endothelial cell lines; a new in vitro BBB model for drug targeting

J Drug Target. 2000;8(6):357-70. doi: 10.3109/10611860008997912.

Abstract

Brain capillary endothelial cell lines (TR-BBB) were established from a recently developed transgenic rat harboring temperature-sensitive simian virus 40 (ts SV 40) large T-antigen gene (Tg rat) and used to characterize the endothelial marker, transport activity, and mRNA expression of transporters and tight-junction strand proteins at the blood-brain barrier (BBB). These cell lines expressed active large T-antigen and grew well at 33 degrees C with a doubling-time of about 22-31 hr, but did not grow at 39 degrees C. TR-BBBs expressed the typical endothelial marker, von Willebrand factor, and exhibited acetylated low-density lipoprotein uptake activity. Although the gamma-glutamyltranspeptidase activity in TR-BBBs was approximately 13% of that of the brain capillary fraction of a normal rat, it was localized in the apical side, suggesting that it reflects the functional polarity of the in vivo BBB. The mRNA of tight-junction strand proteins such as claudine-5, occludin, and junctional adhesion molecule are expressed in TR-BBB13. Drug efflux transporter, P-glycoprotein, with a molecular weight of 170 kDa was expressed in all TR-BBBs and mdr 1a, mdr 1b, and mdr 2 mRNA were detected in TR-BBBs using RT-PCR. Moreover, mrp1 mRNA was expressed in all TR-BBBs. Influx transporter, GLUT-1, expressed at 55 kDa was revealed by Western blot analysis. It had 3-O-methyl-D-glucose (3-OMG) uptake activity which was concentration-dependent with a Michaelis-Menten constant of 9.86 +/- 1.20 mM. The mRNA of large neutral amino acid transporter, which consists of LAT-1 and 4F2hc was expressed in TR-BBBs. In conclusion, the conditionally immortalized rat brain capillary endothelial cell lines (TR-BBB) had endothelial makers, expressed mRNA for tight-junction strand proteins and the influx and efflux transporters and produced GLUT-1, which is capable of 3-OMG transport activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Animals
  • Animals, Genetically Modified
  • Antigens, Viral, Tumor / metabolism
  • Blood-Brain Barrier / drug effects
  • Blood-Brain Barrier / physiology*
  • Cell Adhesion Molecules / metabolism
  • Cell Line / cytology
  • Cell Line / metabolism*
  • Claudin-5
  • Drug Delivery Systems / methods*
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / metabolism*
  • Glucose Transporter Type 1
  • Guanosine / analogs & derivatives
  • Guanosine / pharmacokinetics*
  • Junctional Adhesion Molecules
  • Male
  • Membrane Proteins / metabolism
  • Monosaccharide Transport Proteins / metabolism
  • Occludin
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Wistar

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Antigens, Viral, Tumor
  • Cell Adhesion Molecules
  • Claudin-5
  • Cldn5 protein, rat
  • Glucose Transporter Type 1
  • Junctional Adhesion Molecules
  • Membrane Proteins
  • Monosaccharide Transport Proteins
  • Occludin
  • Ocln protein, rat
  • RNA, Messenger
  • Slc2a1 protein, rat
  • 3'-O-methylguanosine
  • Guanosine