https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2017/08/IL-17A.png 368 655 Linhda Coulevard https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Linhda Coulevard2017-07-14 09:37:162017-08-30 13:48:41Interleukin-17A-induced production of acute serum amyloid A by keratinocytes contributes to psoriasis pathogenesis
Acute-serum Amyloid A (A-SAA), one of the major acute-phase proteins, is mainly produced in the liver but extra-hepatic synthesis involving the skin has been reported. Its expression is regulated by the transcription factors NF-κB, C/EBPβ, STAT3 activated by proinflammatory cytokines.
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2016/03/mw_inhibition-of-keratinocyte-differentiation.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2014-07-10 16:22:302016-09-29 12:48:20Inhibition of keratinocyte differentiation by the synergistic effect of IL-17A, IL-22, IL-1α, TNFα and oncostatin M
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2013/04/mw_Contribution-of-IL-22.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2013-04-11 15:14:312016-09-29 12:52:19Contribution of IL22 to experimental skin inflammation
Focused on in vitro human models, we present the mechanisms of action of IL22 as well as its involvement in structure, metabolism, differentiation, chemotaxis, antibacterial activity, innate immunity, and tissue remodeling of epidermis.
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2016/05/mw_keratinocytes-under-fire.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2012-10-05 16:11:462016-09-29 12:54:49Keratinocytes under fire of proinflammatory cytokines: Bonafide innate immune cells involved in the physiopathology of chronic atopic dermatitis and psoriasis
Specific cytokine environment deregulation plays a central role on skin morphology and innate immunity, moving towards specific pathologies and opening the way to new therapeutic strategies.
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2016/05/mw_Skin-inflammation-induced-by-the-synergistic-action-of-IL-17A.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2010-03-26 15:25:302016-09-29 13:11:35Skin inflammation induced by the synergistic action of IL17A, IL22, OSM, IL1α and TNFα recapitulates some features of psoriasis
Our results demonstrate the important potentiating activities of IL17A, IL22, oncostatin M, TNF-alpha, and IL1alpha on keratinocytes. This is particularly interesting in the context of psoriasis where these cytokines are overexpressed and could synergize to play an important role in upregulation of chemokines and antimicrobial peptides production.
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2016/05/mw_Keratinocytes-as-targets-for-cytokines.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2008-11-20 14:50:532016-09-29 13:14:44Keratinocytes as targets for cytokines in skin inflammation
Current knowledge about the effects of different cytokine families on keratinocytes, and more particularly theirinvolvement in skin inflammation and in the development of inflammatory skin diseases such as psoriasis
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2016/05/mw_Cytokine-induced-CEACAM1-expression.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2008-10-09 13:29:202016-09-29 13:15:20Cytokine-induced CEACAM1 expression on keratinocytes is characteristic for psoriatic skin and contributes to a prolonged lifespan of neutrophils
These results show that cytokine-induced cell-surface expression of CEACAM1 by keratinocytes in the context of a psoriatic environment might contribute to the persistence of neutrophils and thus to ongoing inflammation and the decreased propensity for skin infection, typical for patients with psoriasis.
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2007/09/mw_T-cell-derived-interleukin-22.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2007-09-27 16:47:372016-09-29 13:19:25A role for T cell-derived interleukin 22 in psoriatic skin inflammation
This study indicate that interleukin 22 is a cytokine produced by skin-infiltrating lymphocytes that is potentially involved in initiation and/or maintenance of the pathogenesis of psoriasis.
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2016/05/mw_Oncostatin-M.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2007-04-01 08:56:232016-09-29 13:20:28Oncostatin M secreted by skin infiltrating T lymphocytes is a potent keratinocyte activator involved in skin inflammation
These results demonstrate that OSM and its receptor play an important role in cutaneous inflammatory responses in general and that the specific effects of OSM are associated with distinct inflammatory diseases depending on the cytokine environment.
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2016/05/mw_Keratinocytes-as-targets-for-IL-10-related-cytokines.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2005-12-15 09:47:352016-09-29 13:22:44Keratinocytes as targets for IL-10-related cytokines : a putative role in psoriasis pathogenesis
In this review, we discuss recent knowledge about the effects of cytokines of the IL-10 family on keratinocytes and their potential role in psoriasis, a cutaneous inflammatory disease.
https://cdn-bneoicczbswi.netdna-ssl.com/wp-content/uploads/2016/05/mw_IL-22-inhibits-epidermal-differentiation.jpg 368 655 Julie https://www.bioalternatives.com/wp-content/uploads/2017/03/logo-Bioalternatives-1.png Julie2005-03-15 11:15:072016-09-29 13:27:26IL-22 inhibits epidermal differentiation and induces proinflammatory gene expression and migration of human keratinocytes
IL-22 belongs to a family of cytokines structurally related to IL-10, including IL-19, IL-20, IL-24, and IL-26. In contrast to IL-10, IL-22 has proinflammatory activities. IL-22 signals through a class II cytokine receptor composed of an IL-22-binding chain, IL-22RA1, and the IL-10RB subunit, which is shared with the IL-10R.