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001-es BibID:BIBFORM060928
035-os BibID:(WoS)000373072800283 (Scopus)84960114767
Első szerző:Kovács Dóra (Biológus)
Cím:Sebocytes differentially express and secrete adipokines / Dóra Kovács, Marianna Lovászi, Szilárd Póliska, Attila Oláh, Tamás Bíró, Imre Veres, Christos C. Zouboulis, Mona Ståhle, Ralph Rühl, Éva Remenyik, Dániel Törőcsik
Dátum:2016
ISSN:0906-6705
Megjegyzések:In addition to producing sebum, sebocytes link lipid metabolism with inflammation at a cellular level and hence, greatly resemble adipocytes. However, so far no analysis was performed to identify and characterize the adipocyte-associated inflammatory proteins, the members of the adipokine family in sebocytes. Therefore, we determined the expression profile of adipokines (adiponectin, interleukin [IL] 6, resistin, leptin, serpin E1, visfatin, apelin, chemerin, retinol-binding protein 4 [RBP4] and monocyte chemoattractant protein 1 [MCP1]) in sebaceous glands of healthy and various disease-affected (acne, rosacea, melanoma and psoriasis) skin samples. Sebaceous glands in all examined samples expressed adiponectin, IL6, resistin, leptin, serpin E1 and visfatin, but not apelin, chemerin, RBP4 and MCP1. Confirming the presence of the detected adipokines in the human SZ95 sebaceous gland cell line we further characterized their expression and secretion patterns under different stimuli mimicking bacterial invasion (by using Toll-like receptor [TLR] 2 and 4 activators), or by 13-cis retinoic acid (13CRA; also known as isotretinoin), a key anti-acne agent. With the exception of resistin, the expression of all of the detected adipokines (adiponectin, IL6, leptin, serpin E1 and visfatin) could be further regulated at the level of gene expression, showing a close correlation with the secreted protein levels. Besides providing further evidence on similarities between adipocytes and sebocytes, our results strongly suggest that sebocytes are not simply targets of inflammation but may exhibit initiatory and modulatory roles in the inflammatory processes of the skin through the expression and secretion of adipokines.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Adipokine
Inflammation
Sebocyte
Megjelenés:Experimental Dermatology. - 25 : 3 (2016), p. 194-199. -
További szerzők:Lovászi Marianna (1986-) (biológus) Póliska Szilárd (1978-) (biológus) Oláh Attila (1984-) (élettanász) Bíró Tamás (1968-) (élettanász) Veres Imre (1963-) (bőrgyógyász) Zouboulis, Christos C. (1960-) (bőrgyógyász) Ståhle, Mona Rühl, Ralph (1969-) (vegyész) Remenyik Éva (1956-) (bőrgyógyász) Töröcsik Dániel (1979-) (bőrgyógyász)
Pályázati támogatás:NN117020
OTKA
TÁMOP-4.2.2.A-11/1/KONV-2012-0031
TÁMOP
TÁMOP-4.2.4 A/2-11-1-2012-0001
TÁMOP
FP7-PEOPLE-2013-IEF
Egyéb
"Lendület" LP2011-003/2015
Egyéb
Internet cím:DOI
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001-es BibID:BIBFORM074734
035-os BibID:(cikkazonosító)e0198323 (WOS)000435802500016 (Scopus)85048863741
Első szerző:Töröcsik Dániel (bőrgyógyász)
Cím:Genome wide analysis of TLR1/2- and TLR4-activated SZ95 sebocytes reveals a complex immune-competence and identifies serum amyloid A as a marker for activated sebaceous glands / Dániel Törőcsik, Dóra Kovács, Szilárd Póliska, Zita Szentkereszty-Kovács, Marianna Lovászi, Katalin Hegyi, Andrea Szegedi, Christos C. Zouboulis, Mona Ståhle
Dátum:2018
ISSN:1932-6203
Megjegyzések:Toll-like receptors (TLR) 2 and 4 are active in sebaceous glands and play a central role in the development of acne. Still, there is only limited knowledge on their effect on sebocytes. In this work we performed global gene expression profile analysis with functional clustering of the differentially regulated genes of TLR1/2 (PAM3CSK4)- and TLR4 (lipopolysaccharide [LPS])-activated SZ95 sebocytes. Both TLR1/2- and 4-activation promoted inflammation in a similar manner already at an early time-point (6 hours), regulating genes involved in inflammation, wound healing and chemotaxis reflecting a more complex cytokine and chemokine regulation than previously known. Importantly, lipid metabolism, the primary feature of sebocytes, was affected at the level of gene expression only at a later time point (24 hours) indicating that sebocytes prioritize to exert a pro-inflammatory phenotype when confronted with a danger signal. Supporting the biological relevance of our results, a meta-analysis revealed that the genes showing the strongest up-regulation were also found up-regulated in acne. Of these genes, serum amyloid A 1/2 (SAA1/2) was confirmed to be a suitable protein marker for in vivo activated sebocytes, underlining their immune-competence, which is structurally defined within sebaceous glands of acne and rosacea skin samples. Altogether our findings demonstrate that sebocytes are not only positioned at the end point of inflammation but are actively involved in shaping the inflammatory response with putative diagnostic and therapeutic relevance.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Acne
Gene expression
Sebaceous glands
Inflammation
Gene regulation
Inflammatory diseases
Immune response
Lipid metabolism
Megjelenés:Plos One. - 13 : 6 (2018), p. 1-20. -
További szerzők:Kovács Dóra (1988-) (Biológus) Póliska Szilárd (1978-) (biológus) Szentkereszty-Kovács Zita (1988-) (orvos) Lovászi Marianna (1986-) (biológus) Dull Katalin (1983-) (molekuláris biológus, genetikus) Szegedi Andrea (1964-) (bőrgyógyász) Zouboulis, Christos C. (1960-) (bőrgyógyász) Ståhle, Mona
Pályázati támogatás:GINOP-2.3.2-15-2016-00005
GINOP
GINOP-2.3.2-15-2016-00050
GINOP
EFOP-3.6.1-16-2016-00022
EFOP
Internet cím:Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
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