SIRT1 regulates MAPK pathways in vitiligo skin: insight into the molecular pathways of cell survival. Issue 3 (10th January 2014)
- Record Type:
- Journal Article
- Title:
- SIRT1 regulates MAPK pathways in vitiligo skin: insight into the molecular pathways of cell survival. Issue 3 (10th January 2014)
- Main Title:
- SIRT1 regulates MAPK pathways in vitiligo skin: insight into the molecular pathways of cell survival
- Authors:
- Becatti, Matteo
Fiorillo, Claudia
Barygina, Victoria
Cecchi, Cristina
Lotti, Torello
Prignano, Francesca
Silvestro, Agrippino
Nassi, Paolo
Taddei, Niccolò - Abstract:
- <abstract abstract-type="main" id="jcmm12206-abs-0001"> <title>Abstract</title> <p>Vitiligo is an acquired and progressive hypomelanotic disease that manifests as circumscribed depigmented patches on the skin. The aetiology of vitiligo remains unclear, but recent experimental data underline the interactions between melanocytes and other typical skin cells, particularly keratinocytes. Our previous results indicate that keratinocytes from perilesional skin show the features of damaged cells. Sirtuins (silent mating type information regulation 2 homolog) 1, well‐known modulators of lifespan in many species, have a role in gene repression, metabolic control, apoptosis and cell survival, DNA repair, development, inflammation, neuroprotection and healthy ageing. In the literature there is no evidence for SIRT1 signalling in vitiligo and its possible involvement in disease progression. Here, biopsies were taken from the perilesional skin of 16 patients suffering from non‐segmental vitiligo and SIRT1 signalling was investigated in these cells. For the first time, a new SIRT1/Akt, also known as Protein Kinase B (PKB)/mitogen‐activated protein kinase (MAPK) signalling has been revealed in vitiligo. SIRT1 regulates MAPK pathway <italic>via</italic> Akt‐apoptosis signal‐regulating kinase‐1 and down‐regulates pro‐apoptotic molecules, leading to decreased oxidative stress and apoptotic cell death in perilesional vitiligo keratinocytes. We therefore propose SIRT1 activation as a novel way<abstract abstract-type="main" id="jcmm12206-abs-0001"> <title>Abstract</title> <p>Vitiligo is an acquired and progressive hypomelanotic disease that manifests as circumscribed depigmented patches on the skin. The aetiology of vitiligo remains unclear, but recent experimental data underline the interactions between melanocytes and other typical skin cells, particularly keratinocytes. Our previous results indicate that keratinocytes from perilesional skin show the features of damaged cells. Sirtuins (silent mating type information regulation 2 homolog) 1, well‐known modulators of lifespan in many species, have a role in gene repression, metabolic control, apoptosis and cell survival, DNA repair, development, inflammation, neuroprotection and healthy ageing. In the literature there is no evidence for SIRT1 signalling in vitiligo and its possible involvement in disease progression. Here, biopsies were taken from the perilesional skin of 16 patients suffering from non‐segmental vitiligo and SIRT1 signalling was investigated in these cells. For the first time, a new SIRT1/Akt, also known as Protein Kinase B (PKB)/mitogen‐activated protein kinase (MAPK) signalling has been revealed in vitiligo. SIRT1 regulates MAPK pathway <italic>via</italic> Akt‐apoptosis signal‐regulating kinase‐1 and down‐regulates pro‐apoptotic molecules, leading to decreased oxidative stress and apoptotic cell death in perilesional vitiligo keratinocytes. We therefore propose SIRT1 activation as a novel way of protecting perilesional vitiligo keratinocytes from damage.</p> </abstract> … (more)
- Is Part Of:
- Journal of cellular and molecular medicine. Volume 18:Issue 3(2014)
- Journal:
- Journal of cellular and molecular medicine
- Issue:
- Volume 18:Issue 3(2014)
- Issue Display:
- Volume 18, Issue 3 (2014)
- Year:
- 2014
- Volume:
- 18
- Issue:
- 3
- Issue Sort Value:
- 2014-0018-0003-0000
- Page Start:
- 514
- Page End:
- 529
- Publication Date:
- 2014-01-10
- Subjects:
- Cytology
Medicine
Molecular Biology
Cytologie -- Périodiques
Médecine -- Périodiques
Biologie moléculaire -- Périodiques
Cytology -- Periodicals
Medicine -- Periodicals
Molecular biology -- Periodicals
611.01805 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1582-4934 ↗
http://www.blackwell-synergy.com/loi/jcmm ↗
http://www.usc.edu/hsc/nml/e-resources/info/joucelmm.html ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jcmm.12206 ↗
- Languages:
- English
- ISSNs:
- 1582-1838
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.005000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3158.xml