Paracrine crosstalk between endothelial cells and melanocytes through clusterin to inhibit pigmentation

Exp Dermatol. 2018 Jan;27(1):98-100. doi: 10.1111/exd.13443. Epub 2017 Nov 10.

Abstract

Cutaneous vasculature systems play a role in regulating skin pigmentation. We analysed RNA sequencing data to identify novel antimelanogenic factors secreted from endothelial cells and found that one of the secreted factors, clusterin, is highly expressed by HDMECs. To investigate the paracrine effect of clusterin from HDMECs on the regulation of melanogenesis, HDMECs were infected with clusterin or sh-clusterin lentivirus and the HDMEC-derived conditioned media were used to treat normal human melanocytes. It was found that HDMEC-derived clusterin inhibits melanogenesis through MITF/tyrosinase downregulation. The findings here suggest that HDMECs secrete copious amounts of clusterin and that the clusterin is a factor contributing to the inhibitory effect of endothelial cells on melanogenesis via paracrine crosstalk between endothelial cells and melanocytes.

Keywords: HDMEC; Clusterin; Melanocyte; Pigmentation.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Clusterin / metabolism*
  • Endothelial Cells / metabolism*
  • Humans
  • Melanins / metabolism
  • Melanocytes / metabolism*
  • Microphthalmia-Associated Transcription Factor / metabolism
  • Monophenol Monooxygenase / metabolism
  • Pigmentation Disorders / metabolism*
  • Pigmentation*
  • Skin / metabolism
  • Skin Pigmentation
  • Transforming Growth Factor beta1 / metabolism

Substances

  • CLU protein, human
  • Clusterin
  • MITF protein, human
  • Melanins
  • Microphthalmia-Associated Transcription Factor
  • TGFB1 protein, human
  • Transforming Growth Factor beta1
  • Monophenol Monooxygenase