Primary Cilia Negatively Regulate Melanogenesis in Melanocytes and Pigmentation in a Human Skin Model

PLoS One. 2016 Dec 12;11(12):e0168025. doi: 10.1371/journal.pone.0168025. eCollection 2016.

Abstract

The primary cilium is an organelle protruding from the cell body that senses external stimuli including chemical, mechanical, light, osmotic, fluid flow, and gravitational signals. Skin is always exposed to the external environment and responds to external stimuli. Therefore, it is possible that primary cilia have an important role in skin. Ciliogenesis was reported to be involved in developmental processes in skin, such as keratinocyte differentiation and hair formation. However, the relation between skin pigmentation and primary cilia is largely unknown. Here, we observed that increased melanogenesis in melanocytes treated with a melanogenic inducer was inhibited by a ciliogenesis inducer, cytochalasin D, and serum-free culture. However, these inhibitory effects disappeared in GLI2 knockdown cells. In addition, activation of sonic hedgehog (SHH)-smoothened (Smo) signaling pathway by a Smo agonist, SAG inhibited melanin synthesis in melanocytes and pigmentation in a human skin model. On the contrary, an inhibitor of primary cilium formation, ciliobrevin A1, activated melanogenesis in melanocytes. These results suggest that skin pigmentation may be regulated partly by the induction of ciliogenesis through Smo-GLI2 signaling.

MeSH terms

  • Animals
  • Cell Line
  • Cell Line, Tumor
  • Cilia / drug effects
  • Cilia / physiology*
  • Cytochalasin D / pharmacology
  • Hedgehog Proteins / metabolism
  • Humans
  • Kruppel-Like Transcription Factors / metabolism
  • Melanins / biosynthesis*
  • Melanocytes / cytology
  • Melanocytes / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Nuclear Proteins / metabolism
  • Quinazolinones / pharmacology
  • Signal Transduction
  • Skin / cytology*
  • Skin / drug effects
  • Skin / metabolism
  • Skin Physiological Phenomena* / drug effects
  • Skin Pigmentation / drug effects
  • Skin Pigmentation / physiology*
  • Zinc Finger Protein Gli2

Substances

  • GLI2 protein, human
  • Hedgehog Proteins
  • Kruppel-Like Transcription Factors
  • Melanins
  • Nuclear Proteins
  • Quinazolinones
  • SHH protein, human
  • Zinc Finger Protein Gli2
  • ciliobrevin A
  • Cytochalasin D

Grants and funding

This study was supported by grants from the National Research Foundation (NRF- 2013R1A1A1058361), Ministry of Science, ICT and Future Planning, Republic of Korea. All Funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The AmorePacific Corporation (HC, IHB, HJK, YL, TRL) and MEDIPOST corporation (HBJ) provided support in the form of salaries for authors, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.