Regional chemoarchitecture of the brain of lungfishes based on calbindin D-28K and calretinin immunohistochemistry

J Comp Neurol. 2018 Jun 15;526(9):1457-1497. doi: 10.1002/cne.24422. Epub 2018 Mar 23.

Abstract

Lungfishes are the closest living relatives of land vertebrates, and their neuroanatomical organization is particularly relevant for deducing the neural traits that have been conserved, modified, or lost with the transition from fishes to land vertebrates. The immunohistochemical localization of calbindin (CB) and calretinin (CR) provides a powerful method for discerning segregated neuronal populations, fiber tracts, and neuropils and is here applied to the brains of Neoceratodus and Protopterus, representing the two extant orders of lungfishes. The results showed abundant cells containing these proteins in pallial and subpallial telencephalic regions, with particular distinct distribution in the basal ganglia, amygdaloid complex, and septum. Similarly, the distribution of CB and CR containing cells supports the division of the hypothalamus of lungfishes into neuromeric regions, as in tetrapods. The dense concentrations of CB and CR positive cells and fibers highlight the extent of the thalamus. As in other vertebrates, the optic tectum is characterized by numerous CB positive cells and fibers and smaller numbers of CR cells. The so-called cerebellar nucleus contains abundant CB and CR cells with long ascending axons, which raises the possibility that it could be homologized to the secondary gustatory nucleus of other vertebrates. The corpus of the cerebellum is devoid of CB and CR and cells positive for both proteins are found in the cerebellar auricles and the octavolateralis nuclei. Comparison with other vertebrates reveals that lungfishes share most of their features of calcium binding protein distribution with amphibians, particularly with salamanders.

Keywords: RRID AB_10000321; RRID AB_10000340; RRID AB_10000347; RRID AB_2079751; RRID AB_572268; brain evolution; calcium binding proteins; choline acetyltransferase; dipnoans; segmentation; tyrosine hydroxylase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / metabolism
  • Animals
  • Brain / anatomy & histology*
  • Brain / metabolism*
  • Calbindin 1 / metabolism*
  • Calbindin 2 / metabolism*
  • Female
  • Fishes / anatomy & histology*
  • Male
  • Species Specificity
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Calbindin 1
  • Calbindin 2
  • Tyrosine 3-Monooxygenase
  • Acetylcholinesterase