The Lactate Receptor HCA1 Is Present in the Choroid Plexus, the Tela Choroidea, and the Neuroepithelial Lining of the Dorsal Part of the Third Ventricle

Int J Mol Sci. 2020 Sep 4;21(18):6457. doi: 10.3390/ijms21186457.

Abstract

The volume, composition, and movement of the cerebrospinal fluid (CSF) are important for brain physiology, pathology, and diagnostics. Nevertheless, few studies have focused on the main structure that produces CSF, the choroid plexus (CP). Due to the presence of monocarboxylate transporters (MCTs) in the CP, changes in blood and brain lactate levels are reflected in the CSF. A lactate receptor, the hydroxycarboxylic acid receptor 1 (HCA1), is present in the brain, but whether it is located in the CP or in other periventricular structures has not been studied. Here, we investigated the distribution of HCA1 in the cerebral ventricular system using monomeric red fluorescent protein (mRFP)-HCA1 reporter mice. The reporter signal was only detected in the dorsal part of the third ventricle, where strong mRFP-HCA1 labeling was present in cells of the CP, the tela choroidea, and the neuroepithelial ventricular lining. Co-labeling experiments identified these cells as fibroblasts (in the CP, the tela choroidea, and the ventricle lining) and ependymal cells (in the tela choroidea and the ventricle lining). Our data suggest that the HCA1-containing fibroblasts and ependymal cells have the ability to respond to alterations in CSF lactate in body-brain signaling, but also as a sign of neuropathology (e.g., stroke and Alzheimer's disease biomarker).

Keywords: GPR81; HCA1; HCAR1; choroid plexus; dorsal third ventricle; ependymal cells; fibroblasts; lactate; tela choroidea.

MeSH terms

  • Animals
  • Brain / metabolism
  • Cerebral Ventricles / metabolism
  • Cerebral Ventricles / physiology
  • Cerebrospinal Fluid / metabolism
  • Choroid Plexus / metabolism*
  • Choroid Plexus / physiology
  • Fibroblasts / metabolism
  • Humans
  • Lactic Acid / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Receptors, G-Protein-Coupled / metabolism*
  • Third Ventricle / metabolism*
  • Third Ventricle / physiology

Substances

  • HCAR1 protein, human
  • Receptors, G-Protein-Coupled
  • Lactic Acid