Involvement of Pattern Recognition Receptors in the Direct Influence of Bacterial Components and Standard Antiacne Compounds on Human Sebaceous Gland Cells.
Acne Vulgaris
/ drug therapy
Cell Culture Techniques
Humans
Hydrocortisone
/ pharmacology
Inflammation Mediators
/ metabolism
Isotretinoin
/ pharmacology
Lipopolysaccharide Receptors
/ drug effects
Lipopolysaccharides
/ pharmacology
RNA, Messenger
Real-Time Polymerase Chain Reaction
Retinoids
/ pharmacology
Sebaceous Glands
/ drug effects
Teichoic Acids
/ pharmacology
Toll-Like Receptors
/ drug effects
Tretinoin
/ pharmacology
Vitamin A
/ pharmacology
Human sebaceous gland cells
Hydrocortisone
Innate immunity
Retinoids
Toll-like receptors
Journal
Skin pharmacology and physiology
ISSN: 1660-5535
Titre abrégé: Skin Pharmacol Physiol
Pays: Switzerland
ID NLM: 101188418
Informations de publication
Date de publication:
2021
2021
Historique:
received:
10
06
2020
accepted:
22
11
2020
pubmed:
19
2
2021
medline:
27
10
2021
entrez:
18
2
2021
Statut:
ppublish
Résumé
Pattern recognition receptors are involved in innate and adaptive immunity by detecting microbial components. Bacteria have been accused to play a role in inflammatory acne. We investigated the potential involvement of Toll-like receptor (TLR)2, TLR4, TLR6, and CD14 in the direct influence of bacterial components and standard antiacne compounds on human sebocytes. mRNA and protein expression of TLR2, TLR4, TLR6, and CD14 in SZ95 sebocytes was evaluated by real-time qRT-PCR and immunocytochemistry. The effects of lipopolysaccharides (LPS) and lipoteichoic acid on TLR2, TLR4, and CD14 expression and of cytokine/chemokine secretion by 13-cis-retinoic acid, all-trans-retinoic acid, retinol, and hydrocortisone at the mRNA and protein levels were assessed by real-time qRT-PCR and ELISA and verified by cocultivation with neutralizing antibodies. The constitutive expression of TLR2, TLR4, and CD14 in SZ95 sebocytes was augmented by exposure to LPS. Hydrocortisone induced TLR2, but markedly reduced TLR4 expression. 13-cis-retinoic acid and all-trans-retinoic acid regulated IL-6 release. LPS enhanced and hydrocortisone reduced cytokine and chemokine release. Anti-TLR4 and anti-CD14 mAb blocked LPS-induced IL-8 and IL-6 release. Microbial components use pattern recognition receptors to directly activate sebocytes to express a wide range of proinflammatory molecules and especially IL-8 and IL-6 in a TLR4- and CD14-specific manner. Retinoids, but mostly corticosteroids, also use this pathway to exhibit anti-inflammatory effects.
Identifiants
pubmed: 33601383
pii: 000513259
doi: 10.1159/000513259
doi:
Substances chimiques
Inflammation Mediators
0
Lipopolysaccharide Receptors
0
Lipopolysaccharides
0
RNA, Messenger
0
Retinoids
0
Teichoic Acids
0
Toll-Like Receptors
0
Vitamin A
11103-57-4
lipoteichoic acid
56411-57-5
Tretinoin
5688UTC01R
Isotretinoin
EH28UP18IF
Hydrocortisone
WI4X0X7BPJ
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
19-29Informations de copyright
© 2021 S. Karger AG, Basel.