Differential expression of receptors mediating receptor-mediated transcytosis (RMT) in brain microvessels, brain parenchyma and peripheral tissues of the mouse and the human

Fluids Barriers CNS. 2020 Jul 22;17(1):47. doi: 10.1186/s12987-020-00209-0.

Abstract

Receptor-mediated transcytosis (RMT) is a principal pathway for transport of macromolecules essential for brain function across the blood-brain barrier (BBB). Antibodies or peptide ligands which bind RMT receptors are often co-opted for brain delivery of biotherapeutics. Constitutively recycling transferrin receptor (TfR) is a prototype receptor utilized to shuttle therapeutic cargos across the BBB. Several other BBB-expressed receptors have been shown to mediate transcytosis of antibodies or protein ligands including insulin receptor (INSR) and insulin-like growth factor-1 receptor (IGF1R), lipid transporters LRP1, LDLR, LRP8 and TMEM30A, solute carrier family transporter SLC3A2/CD98hc and leptin receptor (LEPR). In this study, we analyzed expression patterns of genes encoding RMT receptors in isolated brain microvessels, brain parenchyma and peripheral organs of the mouse and the human using RNA-seq approach. IGF1R, INSR and LRP8 were highly enriched in mouse brain microvessels compared to peripheral tissues. In human brain microvessels only INSR was enriched compared to either the brain or the lung. The expression levels of SLC2A1, LRP1, IGF1R, LRP8 and TFRC were significantly higher in the mouse compared to human brain microvessels. The protein expression of these receptors analyzed by Western blot and immunofluorescent staining of the brain microvessels correlated with their transcript abundance. This study provides a molecular transcriptomics map of key RMT receptors in mouse and human brain microvessels and peripheral tissues, important to translational studies of biodistribution, efficacy and safety of antibodies developed against these receptors.

Keywords: Blood–brain barrier; IGF1R; Isolated brain microvessels; Mouse and human species; RNAseq; Receptor-mediated transcytosis; Transferrin receptor.

MeSH terms

  • Aged
  • Animals
  • Antigens, CD / metabolism
  • Blood-Brain Barrier / metabolism*
  • Brain / blood supply
  • Brain / metabolism*
  • Female
  • Humans
  • Low Density Lipoprotein Receptor-Related Protein-1 / metabolism
  • Lung / blood supply
  • Lung / metabolism*
  • Male
  • Mice, Inbred C57BL
  • Microvessels / metabolism*
  • Parenchymal Tissue / blood supply
  • Parenchymal Tissue / metabolism*
  • Receptor, IGF Type 1
  • Receptors, Cell Surface / metabolism*
  • Receptors, Transferrin / metabolism
  • Spleen / blood supply
  • Spleen / metabolism
  • Transcytosis*

Substances

  • Antigens, CD
  • CD71 antigen
  • IGF1R protein, human
  • LRP1 protein, human
  • Low Density Lipoprotein Receptor-Related Protein-1
  • Receptors, Cell Surface
  • Receptors, Transferrin
  • Receptor, IGF Type 1