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Aberrant extracellular signal-regulated kinase (ERK) 5 signaling in hippocampus of suicide subjects.

Aberrant extracellular signal-regulated kinase (ERK) 5 signaling in hippocampus of suicide subjects. Research Abstract Details 

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  • Aberrant extracellular signal-regulated kinase (ERK) 5 signaling in hippocampus of suicide subjects. Abstract Text:

    yogesh dwivediYogesh Dwivedi,hooriyah s rizaviHooriyah S Rizavi,tara teppenTara Teppen,nobuyuki sasakiNobuyuki Sasaki,hu chenHu Chen,hui zhangHui Zhang,rosalinda c robertsRosalinda C Roberts,robert r conleyRobert R Conley,ghanshyam n pandeyGhanshyam N Pandey,yogesh dwivediYogesh Dwivedi,hooriyah s rizaviHooriyah S Rizavi,tara teppenTara Teppen,nobuyuki sasakiNobuyuki Sasaki,hu chenHu Chen,hui zhangHui Zhang,rosalinda c robertsRosalinda C Roberts,robert r conleyRobert R Conley,ghanshyam n pandeyGhanshyam N Pandey,

    Extracellular signal-regulated kinase 5 (ERK5), the newest member of the mitogen-activated protein (MAP) kinase family, is regulated differently than the other MAP kinases. Emerging evidence suggest the role of ERK5 signaling in promoting cell proliferation, differentiation, neuronal survival, and neuroprotection. The present study investigates whether suicide brain is associated with alterations in components of the ERK5 signaling cascade. In the prefrontal cortex (PFC) and hippocampus of suicide subjects (n=28) and nonpsychiatric control subjects (n=21), we examined the catalytic activities and protein levels of ERK5 and upstream MAP kinase kinase MEK5 in various subcellular fractions; mRNA levels of ERK5 in total RNA; and DNA-binding activity of myocyte enhancer factor (MEF)2C, a substrate of ERK5. In the hippocampus of suicide subjects, we observed that catalytic activity of ERK5 was decreased in cytosolic and nuclear fractions, whereas catalytic activity of MEK5 was decreased in the total fraction. Further, decreased mRNA and protein levels of ERK5, but no change in protein level of MEK5 were noted. A decrease in MEF2C-DNA-binding activity in the nuclear fraction was also observed. No significant alterations were noted in the PFC of suicide subjects. The observed changes were not related to a specific psychiatric diagnosis. Our findings of reduced activation and/or expression of ERK5 and MEK5, and reduced MEF2C-DNA-binding activity demonstrate abnormalities in ERK5 signaling in hippocampus of suicide subjects and suggest possible involvement of this aberrant signaling in pathogenic mechanisms of suicide.

    Aberrant extracellular signal-regulated kinase (ERK) 5 signaling in hippocampus of suicide subjects. Publishing Authors By Initials

    y dwivediY Dwivedi,hs rizaviHS Rizavi,t teppenT Teppen,n sasakiN Sasaki,h chenH Chen,h zhangH Zhang,rc robertsRC Roberts,rr conleyRR Conley,gn pandeyGN Pandey,y dwivediY Dwivedi,hs rizaviHS Rizavi,t teppenT Teppen,n sasakiN Sasaki,h chenH Chen,h zhangH Zhang,rc robertsRC Roberts,rr conleyRR Conley,gn pandeyGN Pandey,

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    Aberrant extracellular signal-regulated kinase (ERK) 5 signaling in hippocampus of suicide subjects. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Neuropsychopharmacology : official publication of

    VOLUME: 32

    Page Numbers: 2338-50

    Journal Abbreviation: Neuropsychopharmacology

    ISSN: 0893-133X

    DAY: 7

    MONTH: 03

    YEAR: 2007

    Aberrant extracellular signal-regulated kinase (ERK) 5 signaling in hippocampus of suicide subjects. Information

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    LANGUAGE: eng

    NlmUniqueID: 8904907

    Aberrant extracellular signal-regulated kinase (ERK) 5 signaling in hippocampus of suicide subjects. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: Aberrant extracellular signal-regulated kinase (ERK) 5 signaling in hippocampus of suicide subjects. Information

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    Grant and Affiliation Information for Aberrant extracellular signal-regulated kinase (ERK) 5 signaling in hippocampus of suicide subjects.

    AFFILIATION: Department of Psychiatry, Psychiatric Institute, University of Illinois at Chicago, Chicago, IL 60612, USA. ydwivedi@psych.uic.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIMH

    GRANT: R01MH60744

    ACRONYM: MH

    MEDLINETA: Neuropsychopharmacology

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