Erythrocyte/HEPG2-type glucose transporter is concentrated in cells of blood-tissue barriers

https://doi.org/10.1016/S0006-291X(05)81022-8Get rights and content

In search of possible diverse roles of glucose transporters(GT's), we examined whether any GT's are present in blood-tissue barriers where selective flow of glucose from blood to tissue cells is critically important. We found in rat that the erythrocyte/HepG2-type GT is localized in all the limiting plasma membranes known to serve as blood-tissue barriers, whether the barriers are endothelial type(brain, iris, inner retina, peripheral nerve) or epithelial type(choroid plexus, ciliary body, outer retina, peripheral nerve, placenta), except for plasma membranes in testis and thymus where no appreciable amount of the GT was found. The erythrocyte/HepG2-type GT may play a vital role for the entry of glucose into these firmly guarded tissues.

References (30)

  • BalyD.L. et al.

    Biochim. Biophys. Acta

    (1988)
  • KasaharaM. et al.

    J. Boil. Chem.

    (1977)
  • KasaharaM. et al.

    Biochem. Biophys. Res. Commun.

    (1985)
  • RaviolaG.

    Exp. Eye Res.

    (1977)
  • SaseS. et al.

    Biochim. Biophys. Acta

    (1982)
  • EzakiO. et al.

    J. Biol. Chem.

    (1986)
  • MuecklerM. et al.

    Science

    (1985)
  • HedigerM.A. et al.

    Nature

    (1987)
  • BellG.I. et al.

    Diabetes Care

    (1990)
  • ThorensB. et al.

    Diabetes Care

    (1990)
  • BetzA.L. et al.

    ann. Rev. Physiol.

    (1986)
  • FishmanR.A.

    Cerebrospinal Fluid in Diseases of the Nervous System

    (1980)
  • BöckP. et al.

    Histochemie

    (1971)
  • FaberJ.J. et al.

    Placental Physiology

    (1983)
  • DymM.

    Anat. Rec.

    (1973)
  • Cited by (154)

    • Paclitaxel-loaded ginsenoside Rg3 liposomes for drug-resistant cancer therapy by dual targeting of the tumor microenvironment and cancer cells

      2023, Journal of Advanced Research
      Citation Excerpt :

      Various transporters, including glucose transporters, mannose receptors, low-density lipoprotein receptors, transferrin receptors, and albumin-binding proteins, may serve as drug delivery portal [36]. Particularly, GLUT-1 is highly expressed in malignant cells and endothelial cells of tumor-vessels associated with neoplasms [37-40], where it mediates the transport of glucose as well as other similar substances [36,41]. Rg3 has a hydrophobic domain with a steroid structure in character with that of cholesterol which is the indispensable main ingredient of liposomes and a hydrophilic domain with two glucosyl groups.

    • Interaction of glucose sensing and leptin action in the brain

      2020, Molecular Metabolism
      Citation Excerpt :

      The brain preferentially utilizes glucose as its energy source and all six isoforms of the facilitated glucose transporters are found in the brain [1]. Transport of glucose across the blood–brain barrier is mediated by endothelial glucose transporter-1 (GLUT1) [2], and cellular glucose uptake by astrocytes and neurons is primarily accomplished through GLUT1 and glucose transporter-3, respectively [3]. While it is traditionally believed that glucose enters neurons directly and undergoes glycolysis to form pyruvate and provide neuronal fuel, it is alternatively demonstrated that l-lactate serves as an energy substrate in neurons [4,5].

    • Solute carrier transporters: the metabolic gatekeepers of immune cells

      2020, Acta Pharmaceutica Sinica B
      Citation Excerpt :

      While GLUT6 was previously reported to mediate glucose uptake in endometrial cancer cells65, at least in macrophages, the lysosomally located GLUT6 is not a true glucose transporter, and its physiological roles in immune cells still need to be clarified further64. The information reviewed above glucose transporters involved in immune cells are summarized in Table 166–86,87-119. Glutamine is one of the most abundant amino acids in circulation.

    • Influence of glucose transporter 1 activity inhibition on neuroblastoma in vitro

      2019, Gene
      Citation Excerpt :

      GLUTs are the main carriers of glucose uptake into cells. In the GLUT family, GLUT1 is responsible for primary glucose uptake and maintenance of basal glucose metabolism in cells (Takata et al., 1990). Previous studies showed that GLUT1 activity inhibition by WZB117 effectively reduced glycolysis and cell proliferation, induced cell-cycle arrest in laryngeal carcinoma and lung cancer (Zhou et al., 2009; Liu et al., 2012).

    View all citing articles on Scopus
    View full text