Literature DB >> 18677317

The kinase p38 alpha serves cell type-specific inflammatory functions in skin injury and coordinates pro- and anti-inflammatory gene expression.

Chun Kim1, Yasuyo Sano, Kristina Todorova, Bradley A Carlson, Luis Arpa, Antonio Celada, Toby Lawrence, Kinya Otsu, Janice L Brissette, J Simon C Arthur, Jin Mo Park.   

Abstract

The mitogen-activated protein kinase p38 mediates cellular responses to injurious stress and immune signaling. Among the many p38 isoforms, p38 alpha is the most widely expressed in adult tissues and can be targeted by various pharmacological inhibitors. Here we investigated how p38 alpha activation is linked to cell type-specific outputs in mouse models of cutaneous inflammation. We found that both myeloid and epithelial p38 elicit inflammatory responses, yet p38 alpha signaling in each cell type served distinct inflammatory functions and varied depending on the mode of skin irritation. In addition, myeloid p38 alpha limited acute inflammation via activation of anti-inflammatory gene expression dependent on mitogen- and stress-activated kinases. Our results suggest a dual function for p38 alpha in the regulation of inflammation and show mixed potential for its inhibition as a therapeutic strategy.

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Year:  2008        PMID: 18677317      PMCID: PMC2587092          DOI: 10.1038/ni.1640

Source DB:  PubMed          Journal:  Nat Immunol        ISSN: 1529-2908            Impact factor:   25.606


  49 in total

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Review 2.  The many paths to p38 mitogen-activated protein kinase activation in the immune system.

Authors:  Jonathan D Ashwell
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4.  Conditional gene targeting in macrophages and granulocytes using LysMcre mice.

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Journal:  Transgenic Res       Date:  1999-08       Impact factor: 2.788

Review 5.  Potential adverse effects associated with inhibition of p38alpha/beta MAP kinases.

Authors:  Donna M Dambach
Journal:  Curr Top Med Chem       Date:  2005       Impact factor: 3.295

6.  Essential role of MAPK phosphatase-1 in the negative control of innate immune responses.

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7.  A MAP kinase targeted by endotoxin and hyperosmolarity in mammalian cells.

Authors:  J Han; J D Lee; L Bibbs; R J Ulevitch
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Journal:  Proc Natl Acad Sci U S A       Date:  2006-02-06       Impact factor: 11.205

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Journal:  J Exp Med       Date:  2005-12-27       Impact factor: 14.307

10.  Dual specificity phosphatase 1 (DUSP1) regulates a subset of LPS-induced genes and protects mice from lethal endotoxin shock.

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  133 in total

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Authors:  Pengyu Huang; Jiahuai Han; Lijian Hui
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3.  Taurine attenuates liver injury by downregulating phosphorylated p38 MAPK of Kupffer cells in rats with severe acute pancreatitis.

Authors:  Sidong Wei; Qingyong Huang; Jinzheng Li; Zuojin Liu; Haibo You; Yong Chen; Jianping Gong
Journal:  Inflammation       Date:  2012-04       Impact factor: 4.092

4.  p38 MAPK activation is downstream of the loss of intercellular adhesion in pemphigus vulgaris.

Authors:  Xuming Mao; Yasuyo Sano; Jin Mo Park; Aimee S Payne
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5.  The p38 MAP Kinase Family as Regulators of Proinflammatory Cytokine Production in Degenerative Diseases of the CNS.

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6.  Sex-specific control of central nervous system autoimmunity by p38 mitogen-activated protein kinase signaling in myeloid cells.

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Journal:  Ann Neurol       Date:  2014-01       Impact factor: 10.422

Review 7.  Mitogen-activated protein kinase p38 in HIV infection and associated brain injury.

Authors:  Kathryn E Medders; Marcus Kaul
Journal:  J Neuroimmune Pharmacol       Date:  2011-02-01       Impact factor: 4.147

Review 8.  Targeting innate immunity protein kinase signalling in inflammation.

Authors:  Matthias Gaestel; Alexey Kotlyarov; Michael Kracht
Journal:  Nat Rev Drug Discov       Date:  2009-06       Impact factor: 84.694

9.  MSK1 and MSK2 inhibit lipopolysaccharide-induced prostaglandin production via an interleukin-10 feedback loop.

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Journal:  Mol Cell Biol       Date:  2013-02-04       Impact factor: 4.272

10.  Distinct effects of p38alpha deletion in myeloid lineage and gut epithelia in mouse models of inflammatory bowel disease.

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