Cited by 269Acne and Rosacea Treatments and EffectsDermatology and Skin DiseasesInflammatory mediators and NSAID effects

Enzymes involved in the biosynthesis of leukotriene B4 and prostaglandin E2 are active in sebaceous glands

Alestas, Theodosios, Ganceviciene, Ruta, Fimmel, Sabine, Müller-Decker, Karin, Zouboulis, Christos C.·2006·Journal of Molecular Medicine

Abstract

The expression of enzymes involved in leukotriene and prostaglandin signalling pathways, of interleukins 6 and 8 and of peroxisome proliferator-activated receptors in sebaceous glands of acne-involved facial skin was compared with those of non-involved skin of acne patients and of healthy individuals. Moreover, 5-lipoxygenase and leukotriene A(4) hydrolase were expressed at mRNA and protein levels in vivo and in SZ95 sebocytes in vitro (leukotriene A(4) hydrolase > 5-lipoxygenase), while 15-lipoxygenase-1 was only detected in cultured sebocytes. Cyclooxygenase-1 and cyclooxygenase-2 were also present. Peroxisome proliferator-activated receptors were constitutively expressed. Enhanced 5-lipoxygenase, cyclooxygenase 2 and interleukin 6 expression was detected in acne-involved facial skin. Arachidonic acid stimulated leukotriene B(4) and interleukin 6 release as well as prostaglandin E(2) biosynthesis in SZ95 sebocytes, induced abundant increase in neutral lipids and down-regulated peroxisome proliferator-activated receptor-alpha, but not receptor-gamma1 mRNA levels, which were the predominant peroxisome proliferator-activated receptor isotypes in SZ95 sebocytes. In conclusion, human sebocytes possess the enzyme machinery for functional leukotriene and prostaglandin pathways. A comprehensive link between inflammation and sebaceous lipid synthesis is provided.

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Crossref · 10.1007/s00109-005-0715-8

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  • Activation of TLR-2 and -4, which are expressed in sebocytes, plays a crucial role in the inflammatory properties of sebocytes.

    “in which the activation of TLR-2 and -4, shown to also be expressed in sebocytes, play a crucial role.46-48”

    From Sebaceous-immunobiology is orchestrated by sebum lipids (2017) · cites this paper as [47]

  • PPAR-α, -δ, -γ1 and -γ2 are all expressed in sebocytes.

    “PPARs with all three isoforms namely PPAR-α, -δ, -γ1 and -γ2 which are all expressed in sebocytes47”

    From Sebaceous-immunobiology is orchestrated by sebum lipids (2017) · cites this paper as [47]

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References 55 · Cited by 269

Authors
Alestas, T., Ganceviciene, R., Fimmel, S., Müller-Decker, K., & Zouboulis, C. C.
Affiliations
  • Stiftung Charité (DE)
  • Charité – Universitätsmedizin Berlin (DE)
  • Städtisches Klinikum Dessau (DE)
Corresponding author
Zouboulis, Christos C.
Venue
Journal of Molecular Medicine
Published
2005-12-31
Volume
84
Issue
1
Pages
75-87
ISSN
  • 0946-2716 (ISSN-L)
  • 1432-1440
OpenAlex
W2158599779
Cited by
269
References
55
Citations by year
2026: 3 · 2025: 11 · 2024: 9 · 2023: 7 · 2022: 12 · 2021: 17 · 2020: 13 · 2019: 12 · 2018: 14 · 2017: 16 · 2016: 11 · 2015: 17 · 2014: 22 · 2013: 13 · 2012: 11
FWCI
13.62
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Molecular Medicine (publishedVersion)
  • PubMed (publishedVersion)
Funders
Dermatology Foundation
Topics
  • Health Sciences › Medicine › Dermatology › Acne and Rosacea Treatments and Effects
  • Health Sciences › Medicine › Dermatology › Dermatology and Skin Diseases
  • Health Sciences › Medicine › Pharmacology › Inflammatory mediators and NSAID effects
Keywords
sebaceous glands, sebocytes, acne, leukotriene B4, prostaglandin E2, 5-lipoxygenase, leukotriene A4 hydrolase, 15-lipoxygenase-1, cyclooxygenase-2, cyclooxygenase-1, peroxisome proliferator-activated receptors, interleukin-6, interleukin-8, arachidonic acid, inflammation
MeSH terms
Acne Vulgaris, Adolescent, Adult, Arachidonate 5-Lipoxygenase, Cells, Cultured, Epoxide Hydrolases, Female, Humans, Inflammation, Leukotriene B4, Male, Membrane Proteins, Sebaceous Glands, Dinoprostone, Interleukin-6, Interleukin-8, Arachidonic Acid, Protein Isoforms, Peroxisome Proliferator-Activated Receptors, Cyclooxygenase 2

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