Common and diverse elements of ion channels and receptors underlying electrical activity in endocrine pituitary cells

Mol Cell Endocrinol. 2018 Mar 5:463:23-36. doi: 10.1016/j.mce.2017.06.022. Epub 2017 Jun 24.

Abstract

The pituitary gland contains six types of endocrine cells defined by hormones they secrete: corticotrophs, melanotrophs, gonadotrophs, thyrotrophs, somatotrophs, and lactotrophs. All these cell types are electrically excitable, and voltage-gated calcium influx is the major trigger for their hormone secretion. Along with hormone intracellular content, G-protein-coupled receptor and ion channel expression can also be considered as defining cell type identity. While many aspects of the developmental and activity dependent regulation of hormone and G-protein-coupled receptor expression have been elucidated, much less is known about the regulation of the ion channels needed for excitation-secretion coupling in these cells. We compare the spontaneous and receptor-controlled patterns of electrical signaling among endocrine pituitary cell types, including insights gained from mathematical modeling. We argue that a common set of ionic currents unites these cells, while differential expression of another subset of ionic currents could underlie cell type-specific patterns. We demonstrate these ideas using a generic mathematical model, showing that it reproduces many observed features of pituitary electrical signaling. Mapping these observations to the developmental lineage suggests possible modes of regulation that may give rise to mature pituitary cell types.

Keywords: Action potentials; Calcium signaling; G-protein coupled receptors; Ion channels; Mathematical modeling; Voltage-gated calcium influx.

Publication types

  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Animals
  • Electrophysiological Phenomena*
  • Endocrine Cells / metabolism*
  • Hormones / metabolism
  • Humans
  • Ion Channels / metabolism*
  • Pituitary Gland / cytology*
  • Pituitary Gland / metabolism*
  • Receptors, G-Protein-Coupled / metabolism*

Substances

  • Hormones
  • Ion Channels
  • Receptors, G-Protein-Coupled