Rapid GLUT-1 mediated glucose transport in erythrocytes from the grey-headed fruit bat (Pteropus poliocephalus)

Comp Biochem Physiol A Mol Integr Physiol. 2000 May;126(1):45-55. doi: 10.1016/s1095-6433(00)00177-x.

Abstract

D-Glucose entry into erythrocytes from adult grey-headed flying fox fruit bats (Pteropus poliocephalus) was rapid and showed saturation at high substrate concentrations. Kinetic parameters were estimated from the concentration dependence of initial rates of zero-trans D-glucose entry at 5.5 degrees C as Michaelis constant (K(m)) 1. 64+/-0.56 mM, and maximal velocity (V(max)) 1162+/-152 micromol.l. cell water(-1).min(-1). D-Glucose entry was inhibited by cytochalasin B; mass law analysis of D-glucose-displaceable cytochalasin B binding gave values of K(d) 37.1+/-5.0 nM and B(max) 361.2+/-9.1 pmol/mg membrane protein. Entry of 2-deoxy-D-glucose, and 3-O-methyl-D-glucose, into P. poliocephalus red cells was rapid, entry of D-fructose was very slow. Glucose transporter polypeptides were identified on immunoblots as a band M(r) 47000-54000 and their identity confirmed by D-glucose-sensitive photolabeling of membranes with [3H]-cytochalasin B. Peptide-N-glycanase F digestion of both human and bat erythrocyte membranes generated GLUT-1-derived bands M(r) 37000. Trypsin digestion of human and fruit bat erythrocyte membranes generated fragmentation patterns consistent with similar GLUT-1 polypeptide structures in both species. Erythrocytes from adult Australian ghost bats (Macroderma gigas), a carnivorous microchiropteran bat, also expressed high levels of GLUT-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amidohydrolases / metabolism
  • Animals
  • Binding, Competitive / drug effects
  • Biological Transport / drug effects
  • Cell Membrane Permeability
  • Chiroptera / metabolism*
  • Cytochalasin B / chemistry
  • Cytochalasin B / pharmacology
  • Erythrocyte Membrane / chemistry
  • Erythrocyte Membrane / metabolism
  • Erythrocytes / drug effects
  • Erythrocytes / metabolism*
  • Glucose / metabolism*
  • Glucose / pharmacokinetics
  • Glucose Transporter Type 1
  • Immunoblotting
  • Monosaccharide Transport Proteins / analysis
  • Monosaccharide Transport Proteins / metabolism*
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase
  • Photochemistry
  • Tritium
  • Trypsin / metabolism

Substances

  • Glucose Transporter Type 1
  • Monosaccharide Transport Proteins
  • Tritium
  • Cytochalasin B
  • Trypsin
  • Amidohydrolases
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase
  • Glucose