Telocytes constitute a widespread interstitial meshwork in the lamina propria and underlying striated muscle of human tongue

Sci Rep. 2019 Apr 10;9(1):5858. doi: 10.1038/s41598-019-42415-3.

Abstract

Telocytes have recently emerged as unique interstitial cells defined by their extremely long, thin and moniliform prolongations termed telopodes. Despite growing evidence that these cells consistently reside in the stromal compartment of various organs from human beings, studies dealing with telocytes in structures of the oral cavity are scarce. Hence, the present morphologic study was undertaken to explore for the first time the presence and specific localization of telocytes within tissues of the normal human tongue, a complex muscular organ whose main functions include taste, speech, and food manipulation in the oral cavity. Telocytes were initially identified by CD34 immunostaining and confirmed by CD34/PDGFRα double immunofluorescence and transmission electron microscopy. CD34+/PDGFRα+ telocytes were organized in interstitial meshworks either in the tongue lamina propria or in the underlying striated muscle. Lingual telocytes were immunonegative for CD31, c-kit and α-SMA. Telopodes were finely distributed throughout the stromal space and concentrated beneath the lingual epithelium and around CD31+ vessels, skeletal muscle bundles/fibers, and intramuscular nerves and ganglia. They also enveloped salivary gland units outside the α-SMA+ myoepithelial cells and delimited lymphoid aggregates. These findings establish telocytes as a previously overlooked interstitial cell population worth investigating further in the setting of human tongue pathophysiology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antigens, CD34 / metabolism
  • Female
  • Humans
  • Immunophenotyping
  • Male
  • Microscopy, Electron, Transmission
  • Microscopy, Fluorescence
  • Middle Aged
  • Mucous Membrane / cytology
  • Mucous Membrane / metabolism
  • Mucous Membrane / pathology
  • Proto-Oncogene Proteins c-kit / metabolism
  • Receptor, Platelet-Derived Growth Factor alpha / metabolism
  • Telocytes / metabolism*
  • Telocytes / pathology
  • Telocytes / ultrastructure
  • Telopodes / metabolism
  • Telopodes / pathology
  • Tongue / metabolism*
  • Tongue / pathology

Substances

  • Antigens, CD34
  • Proto-Oncogene Proteins c-kit
  • Receptor, Platelet-Derived Growth Factor alpha