Histamine metabolism and transport are deranged in human keratinocytes in oral lichen planus

Br J Dermatol. 2017 May;176(5):1213-1223. doi: 10.1111/bjd.14995. Epub 2017 Mar 22.

Abstract

Background: Recent reports have indicated that nonimmune cells can produce low concentrations of histamine. This observation, together with the discovery of the high-affinity histamine H4 receptor (H4 R), has added additional layers of complexity to our understanding of histamine signalling. Human oral keratinocytes (HOKs) possess a uniform H4 R pattern, which is deranged in oral lichen planus (OLP).

Objectives: To investigate histamine metabolism and transport in HOKs of healthy controls and patients with OLP.

Methods: Tissue sections and cultured primary HOKs were studied using immunostaining, quantitative real-time polymerase chain reaction and confocal microscopy. Histamine levels were analysed using high-performance liquid chromatography.

Results: l-histidine decarboxylase (HDC) and organic cation transporter (OCT)3 were increased in mRNA and protein levels in patients with OLP compared with controls. In contrast, histamine N-methyltransferase (HNMT) immunoreactivity was decreased in OLP. OCT1/OCT2 and diamine oxidase were not detectable in either tissue sections or in HOKs. Immunolocalization of HDC and OCT3 in HOKs revealed moderate-to-high expression within cytoplasm and cell boundaries. Stimulation with lipopolysaccharide (LPS) or interferon-γ upregulated HDC-gene transcript in HOKs, whereas this was downregulated with high histamine concentration and tumour necrosis factor-α. LPS induced a dose-dependent release of low histamine in HOKs, while high histamine concentration downregulated epithelial adhesion proteins.

Conclusions: HOKs are histamine-producing cells. They release histamine via OCT3 channels in concentrations too low to activate the classical low-affinity H1 R and H2 R, but high enough to stimulate the high-affinity H4 R in autocrine and paracrine modes. The substantially deranged histamine metabolism and transport in OLP could, in part, contribute to the disease pathogenesis.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Amine Oxidase (Copper-Containing) / metabolism
  • Cells, Cultured
  • Cytosol / metabolism
  • Down-Regulation / physiology
  • Histamine / metabolism*
  • Histamine N-Methyltransferase / metabolism
  • Histidine Decarboxylase / metabolism
  • Humans
  • Interferon-gamma / pharmacology
  • Keratinocytes / metabolism*
  • Lichen Planus, Oral / etiology
  • Lichen Planus, Oral / metabolism*
  • Lipopolysaccharides / pharmacology
  • Middle Aged
  • Organic Cation Transport Proteins / metabolism
  • RNA, Messenger / metabolism
  • Up-Regulation / physiology
  • Young Adult

Substances

  • Lipopolysaccharides
  • Organic Cation Transport Proteins
  • RNA, Messenger
  • solute carrier family 22 (organic cation transporter), member 3
  • Histamine
  • Interferon-gamma
  • Amine Oxidase (Copper-Containing)
  • Histamine N-Methyltransferase
  • Histidine Decarboxylase