The Expression Pattern of Genes Related to Melanogenesis and Endogenous Opioids in Psoriasis

The melanocortin system is a major regulator of stress responses in the skin and is responsible for the induction of melanin synthesis through activation of melanogenesis enzymes. The expression of both melanocortin system genes and melanogenesis enzyme genes is altered in psoriasis, and the focus h...

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Main Authors: Ulvi Loite, Liisi Raam, Ene Reimann, Paula Reemann, Ele Prans, Tanel Traks, Eero Vasar, Helgi Silm, Külli Kingo, Sulev Kõks
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/23/13056
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author Ulvi Loite
Liisi Raam
Ene Reimann
Paula Reemann
Ele Prans
Tanel Traks
Eero Vasar
Helgi Silm
Külli Kingo
Sulev Kõks
author_facet Ulvi Loite
Liisi Raam
Ene Reimann
Paula Reemann
Ele Prans
Tanel Traks
Eero Vasar
Helgi Silm
Külli Kingo
Sulev Kõks
author_sort Ulvi Loite
collection DOAJ
description The melanocortin system is a major regulator of stress responses in the skin and is responsible for the induction of melanin synthesis through activation of melanogenesis enzymes. The expression of both melanocortin system genes and melanogenesis enzyme genes is altered in psoriasis, and the focus here was on twelve genes related to the signal transduction between them. Additionally, five endogenous opioid system genes that are involved in cutaneous inflammation were examined. Quantitative real-time-PCR was utilized to measure mRNA expression in punch biopsies from lesional and non-lesional skin of psoriasis patients and from the skin of healthy control subjects. Most of the genes related to melanogenesis were down-regulated in patients (CREB1, MITF, LEF1, USF1, MAPK14, ICAM1, PIK3CB, RPS6KB1, KIT, and ATRN). Conversely, an up-regulation occurred in the case of opioids (PENK, PDYN, and PNOC). The suppression of genes related to melanogenesis is in agreement with the reported reduction in pigmentation signaling in psoriatic skin and potentially results from the pro-inflammatory environment. The increase in endogenous opioids can be associated with their involvement in inflammatory dysregulation in psoriasis.
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spelling doaj.art-51ab4ca763bf44e694345b46cd9a5e062023-11-23T02:32:26ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-12-0122231305610.3390/ijms222313056The Expression Pattern of Genes Related to Melanogenesis and Endogenous Opioids in PsoriasisUlvi Loite0Liisi Raam1Ene Reimann2Paula Reemann3Ele Prans4Tanel Traks5Eero Vasar6Helgi Silm7Külli Kingo8Sulev Kõks9Department of Dermatology and Venerology, University of Tartu, 31 Raja, 50417 Tartu, EstoniaDepartment of Dermatology and Venerology, University of Tartu, 31 Raja, 50417 Tartu, EstoniaInstitute of Genomics, University of Tartu, 23b/2 Riia, 51010 Tartu, EstoniaDepartment of Dermatology and Venerology, University of Tartu, 31 Raja, 50417 Tartu, EstoniaDepartment of Anaesthesiology and Intensive Care, Tartu University Hospital, 8 L. Puusepa, 51014 Tartu, EstoniaDepartment of Dermatology and Venerology, University of Tartu, 31 Raja, 50417 Tartu, EstoniaDepartment of Physiology, University of Tartu, 19 Ravila Street, 50411 Tartu, EstoniaDepartment of Dermatology and Venerology, University of Tartu, 31 Raja, 50417 Tartu, EstoniaDepartment of Dermatology and Venerology, University of Tartu, 31 Raja, 50417 Tartu, EstoniaThe Perron Institute for Neurological and Translational Science, 8 Verdun St., Nedlands, WA 6009, AustraliaThe melanocortin system is a major regulator of stress responses in the skin and is responsible for the induction of melanin synthesis through activation of melanogenesis enzymes. The expression of both melanocortin system genes and melanogenesis enzyme genes is altered in psoriasis, and the focus here was on twelve genes related to the signal transduction between them. Additionally, five endogenous opioid system genes that are involved in cutaneous inflammation were examined. Quantitative real-time-PCR was utilized to measure mRNA expression in punch biopsies from lesional and non-lesional skin of psoriasis patients and from the skin of healthy control subjects. Most of the genes related to melanogenesis were down-regulated in patients (CREB1, MITF, LEF1, USF1, MAPK14, ICAM1, PIK3CB, RPS6KB1, KIT, and ATRN). Conversely, an up-regulation occurred in the case of opioids (PENK, PDYN, and PNOC). The suppression of genes related to melanogenesis is in agreement with the reported reduction in pigmentation signaling in psoriatic skin and potentially results from the pro-inflammatory environment. The increase in endogenous opioids can be associated with their involvement in inflammatory dysregulation in psoriasis.https://www.mdpi.com/1422-0067/22/23/13056psoriasismelanocortin systemmelanogenesis enzymesendogenous opioid systemmRNA expression analysis
spellingShingle Ulvi Loite
Liisi Raam
Ene Reimann
Paula Reemann
Ele Prans
Tanel Traks
Eero Vasar
Helgi Silm
Külli Kingo
Sulev Kõks
The Expression Pattern of Genes Related to Melanogenesis and Endogenous Opioids in Psoriasis
International Journal of Molecular Sciences
psoriasis
melanocortin system
melanogenesis enzymes
endogenous opioid system
mRNA expression analysis
title The Expression Pattern of Genes Related to Melanogenesis and Endogenous Opioids in Psoriasis
title_full The Expression Pattern of Genes Related to Melanogenesis and Endogenous Opioids in Psoriasis
title_fullStr The Expression Pattern of Genes Related to Melanogenesis and Endogenous Opioids in Psoriasis
title_full_unstemmed The Expression Pattern of Genes Related to Melanogenesis and Endogenous Opioids in Psoriasis
title_short The Expression Pattern of Genes Related to Melanogenesis and Endogenous Opioids in Psoriasis
title_sort expression pattern of genes related to melanogenesis and endogenous opioids in psoriasis
topic psoriasis
melanocortin system
melanogenesis enzymes
endogenous opioid system
mRNA expression analysis
url https://www.mdpi.com/1422-0067/22/23/13056
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