Cited by 76Peroxisome Proliferator-Activated ReceptorsCholesterol and Lipid MetabolismHair Growth and Disorders

Characterization of liver X receptor expression and function in human skin and the pilosebaceous unit

Russell, Louise E., Harrison, Wesley J., Bahta, Adiam W., Zouboulis, Christos C., Burrin, Jacky M., Philpott, Michael P.·2007·Experimental Dermatology

Abstract

Abstract: The nuclear receptors liver X receptor alpha (LXRα) and liver X‐receptor beta (LXRβ) have a well documented role in cholesterol homeostasis and lipid metabolism within tissues and cells including the liver, small intestine and macrophages. In keratinocytes, LXRs have been shown to up‐regulate differentiation in vitro via increased transcription of proteins of the AP1 complex and to down‐regulate proliferation in vivo. In this study, we provide a detailed description of the location and possible role of LXRs within human skin and its associated glands and appendages. Using RT‐PCR, Western blotting and immunohistochemistry, we have demonstrated expression of LXRα and LXRβ mRNA and proteins in whole human skin as well as within a range of primary and immortalized human cell lines derived from human skin, hair follicle and sebaceous glands. Furthermore, we have shown that synthetic LXR specific agonists GW683965 and TO901317 significantly inhibit cell proliferation in primary epidermal keratinocytes, immortalized N/TERT keratinocytes and the immortalized SZ95 sebocyte line, and significantly increase lipogenesis in SZ95 sebocytes. In addition, we showed that the synthetic agonist TO901317 significantly reduced hair growth, in vitro.

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Crossref · 10.1111/j.1600-0625.2007.00612.x

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  • Using LXR ligands such as 22R-hydroxycholesterol increases the expression of key fatty acid synthetases and sterol regulatory element-binding protein-1 (SREBP-1), followed by the accumulation of lipid droplets, a hallmark of sebaceous lipogenesis.

    “Using LXR ligands such as 22R-hydroxycholesterol an increase in the expression of key fatty acid synthetases as well as sterol regulatory element-binding protein-1 (SREBP-1) was observed, followed by the accumulation of lipid droplets, a hallmark of sebaceous lipogenesis.77,78”

    From Sebaceous-immunobiology is orchestrated by sebum lipids (2017) · cites this paper as [77]

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References 48 · Cited by 76

Authors
Russell, L. E., Harrison, W. J., Bahta, A. W., Zouboulis, C. C., Burrin, J. M., & Philpott, M. P.
Affiliations
  • University of London (GB)
  • Städtisches Klinikum Dessau (DE)
Corresponding author
Russell, Louise E.
Venue
Experimental Dermatology
Publisher
Wiley
Published
2007-09-05
Volume
16
Issue
10
Pages
844-852
ISSN
  • 0906-6705 (ISSN-L)
  • 1600-0625
OpenAlex
W1975903787
Cited by
76
References
48
Citations by year
2026: 1 · 2025: 1 · 2024: 4 · 2023: 4 · 2022: 2 · 2021: 4 · 2020: 1 · 2019: 3 · 2018: 2 · 2017: 6 · 2016: 6 · 2015: 7 · 2014: 4 · 2013: 6 · 2012: 4
FWCI
2.39
Type
journal article
Language
en
Open access
closed
Locations
  • Experimental Dermatology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
  • Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
  • Health Sciences › Medicine › Urology › Hair Growth and Disorders
Keywords
liver X receptor alpha, liver X receptor beta, human skin, pilosebaceous unit, sebocytes, keratinocytes, hair follicle, sebaceous glands, LXR agonists, TO901317, cell proliferation, lipogenesis, hair growth, cholesterol homeostasis, lipid metabolism
MeSH terms
Liver X Receptors, Epidermal Cells, Cell Line, Cells, Cultured, DNA-Binding Proteins, Epidermis, Fibroblasts, Hair, Humans, Phenylacetates, Sebaceous Glands, Skin, Sulfonamides, Sweat Glands, Blotting, Western, Keratinocytes, Gene Expression, Receptors, Cytoplasmic and Nuclear, Hair Follicle, Reverse Transcriptase Polymerase Chain Reaction, Cell Proliferation, Lipogenesis, Orphan Nuclear Receptors

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