Literature DB >> 14623496

Apolipoprotein D modulates arachidonic acid signaling in cultured cells: implications for psychiatric disorders.

Elizabeth A Thomas1, Roshni C George, J Gregor Sutcliffe.   

Abstract

Deficiencies in arachidonic acid (AA) parameters have been reported in schizophrenic patients. AA is a primary binding ligand for apolipoprotein D (apoD), which is increased in response to antipsychotic drug treatment and elevated in subjects with schizophrenia and bipolar disorder. In this study, we investigated whether apoD might modulate AA signaling/mobilization in cultured embryonic kidney (HEK) 293T cells. Immunofluorescent labeling revealed both cytosolic and membrane-bound expression of apoD protein in apoD-transfected cells. In cells expressing apoD, phorbal 12-myristate 13-acetate-induced AA release was inhibited compared to controls and membrane levels of AA were elevated, as indicated by the amount of AA maximally incorporated into membrane phospholipids. In addition, exogenous apoD added directly to the incubation media prevented cellular uptake of free [3H]AA. These results suggest that apoD acts to stabilize membrane-associated AA by preventing release and sequestering free AA in the cell. These actions of apoD may be beneficial to psychiatric patients.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14623496     DOI: 10.1016/j.plefa.2003.08.014

Source DB:  PubMed          Journal:  Prostaglandins Leukot Essent Fatty Acids        ISSN: 0952-3278            Impact factor:   4.006


  12 in total

Review 1.  Apolipoprotein D.

Authors:  Eric Rassart; Frederik Desmarais; Ouafa Najyb; Karl-F Bergeron; Catherine Mounier
Journal:  Gene       Date:  2020-06-15       Impact factor: 3.688

Review 2.  Molecular profiling of antipsychotic drug function: convergent mechanisms in the pathology and treatment of psychiatric disorders.

Authors:  Elizabeth A Thomas
Journal:  Mol Neurobiol       Date:  2006-10       Impact factor: 5.590

3.  Apolipoprotein D Internalization Is a Basigin-dependent Mechanism.

Authors:  Ouafa Najyb; Louise Brissette; Eric Rassart
Journal:  J Biol Chem       Date:  2015-04-27       Impact factor: 5.157

4.  Apolipoprotein D is involved in the mechanisms regulating protection from oxidative stress.

Authors:  Maria D Ganfornina; Sonia Do Carmo; Jose M Lora; Sonia Torres-Schumann; Marci Vogel; Maria Allhorn; Constancio González; Michael J Bastiani; Eric Rassart; Diego Sanchez
Journal:  Aging Cell       Date:  2008-04-14       Impact factor: 9.304

5.  Immunohistochemical distribution of somatostatin and somatostatin receptor subtypes (SSTR1-5) in hypothalamus of ApoD knockout mice brain.

Authors:  Ujendra Kumar
Journal:  J Mol Neurosci       Date:  2012-05-12       Impact factor: 3.444

6.  Apolipoprotein D Transgenic Mice Develop Hepatic Steatosis through Activation of PPARγ and Fatty Acid Uptake.

Authors:  Marilyne Labrie; Simon Lalonde; Ouafa Najyb; Maxime Thiery; Caroline Daneault; Chrisitne Des Rosiers; Eric Rassart; Catherine Mounier
Journal:  PLoS One       Date:  2015-06-17       Impact factor: 3.240

Review 7.  Apolipoprotein D takes center stage in the stress response of the aging and degenerative brain.

Authors:  Sarah Dassati; Andreas Waldner; Rüdiger Schweigreiter
Journal:  Neurobiol Aging       Date:  2014-02-05       Impact factor: 4.673

8.  Schwann cell-derived Apolipoprotein D controls the dynamics of post-injury myelin recognition and degradation.

Authors:  Nadia García-Mateo; Maria D Ganfornina; Olimpio Montero; Miguel A Gijón; Robert C Murphy; Diego Sanchez
Journal:  Front Cell Neurosci       Date:  2014-11-11       Impact factor: 5.505

9.  Apolipoprotein D Concentration in Human Plasma during Aging and in Parkinson's Disease: A Cross-Sectional Study.

Authors:  Andreas Waldner; Sarah Dassati; Bernhard Redl; Nicola Smania; Marialuisa Gandolfi
Journal:  Parkinsons Dis       Date:  2018-03-26

10.  Apolipoprotein D Upregulation in Alzheimer's Disease but Not Frontotemporal Dementia.

Authors:  Surabhi Bhatia; Woojin Scott Kim; Claire E Shepherd; Glenda M Halliday
Journal:  J Mol Neurosci       Date:  2018-11-22       Impact factor: 3.444

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.