FASEB J. Integrated DNA Technologies
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published as doi: 10.1096/fj.08-121392.
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Buy
Right arrow All Versions of this Article:
fj.08-121392v1
23/6/1643    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tippmann, F.
Right arrow Articles by Fahrenholz, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tippmann, F.
Right arrow Articles by Fahrenholz, F.
(The FASEB Journal. 2009;23:1643-1654.)
© 2009 FASEB

Up-regulation of the {alpha}-secretase ADAM10 by retinoic acid receptors and acitretin

Frank Tippmann*, Jana Hundt*,1, Anja Schneider{dagger}, Kristina Endres*,2 and Falk Fahrenholz*,2,3

* Institute of Biochemistry, Johannes Gutenberg-University, Mainz, Germany; and

{dagger} Department of Psychiatry and Psychotherapy, University of Medicine and Max-Planck-Institute for Experimental Medicine, Goettingen, Germany

3Correspondence: Institute of Biochemistry, University of Mainz, Becherweg 30, D-55099 Mainz, Germany. E-mail: fahrenho{at}uni-mainz.de

Late-onset Alzheimer’s disease is often connected with nutritional misbalance, such as enhanced cholesterol intake, deficiency in polyunsaturated fatty acids, or hypovitaminosis. The {alpha}-secretase ADAM10 has been found to be regulated by retinoic acid, the bioreactive metabolite of vitamin A. Here we show that retinoids induce gene expression of ADAM10 and {alpha}-secretase activity by nonpermissive retinoid acid receptor/retinoid X receptor (RAR/RXR) heterodimers, whereby {alpha}- and β-isotypes of RAR play a major role. However, ligands of other RXR binding partners, such as the vitamin D receptor, do not stimulate {alpha}-secretase activity. On the basis of these findings, we examined the effect of synthetic retinoids and found a strong enhancement of nonamyloidogenic processing of the amyloid precursor protein by the vitamin A analog acitretin: it stimulated ADAM10 promoter activity with an EC50 of 1.5 µM and led to an increase of mature ADAM10 protein that resulted in a two- to three-fold increase of the ratio between {alpha}- and β-secretase activity in neuroblastoma cells. The {alpha}-secretase stimulation by acitretin was completely inhibited by the ADAM10-specific inhibitor GI254023X. Intracerebral injection of acitretin in APP/PS1–21 transgenic mice led to a reduction of Aβ40 and Aβ42. The results of this study may have clinical relevance because acitretin has been approved for the treatment of psoriasis since 1997 and found generally safe for long-term use in humans.—Tippmann, F., Hundt, J., Schneider, A., Endres, K., Fahrenholz, F. Up-regulation of the {alpha}-secretase ADAM10 by retinoic acid receptors and acitretin.


Key Words: Alzheimer’s disease • amyloid precursor protein • shedding • nuclear receptors • vitamin A







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by The Federation of American Societies for Experimental Biology.