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Publication : Soluble amyloid precursor protein (APP) regulates transthyretin and Klotho gene expression without rescuing the essential function of APP.

First Author  Li H Year  2010
Journal  Proc Natl Acad Sci U S A Volume  107
Issue  40 Pages  17362-7
PubMed ID  20855613 Mgi Jnum  J:165417
Mgi Id  MGI:4837283 Doi  10.1073/pnas.1012568107
Citation  Li H, et al. (2010) Soluble amyloid precursor protein (APP) regulates transthyretin and Klotho gene expression without rescuing the essential function of APP. Proc Natl Acad Sci U S A 107(40):17362-7
abstractText  Amyloidogenic processing of the amyloid precursor protein (APP) generates a large secreted ectodomain fragment (APPsbeta), beta-amyloid (Abeta) peptides, and an APP intracellular domain (AICD). Whereas Abeta is viewed as critical for Alzheimer's disease pathogenesis, the role of other APP processing products remains enigmatic. Of interest, the AICD has been implicated in transcriptional regulation, and N-terminal cleavage of APPsbeta has been suggested to produce an active fragment that may mediate axonal pruning and neuronal cell death. We previously reported that mice deficient in APP and APP-like protein 2 (APLP2) exhibit early postnatal lethality and neuromuscular synapse defects, whereas mice with neuronal conditional deletion of APP and APLP2 are viable. Using transcriptional profiling, we now identify transthyretin (TTR) and Klotho as APP/APLP2-dependent genes whose expression is decreased in loss-of-function states but increased in gain-of-function states. Significantly, by creating an APP knockin allele that expresses only APPsbeta protein, we demonstrate that APPsbeta is not normally cleaved in vivo and is fully capable of mediating the APP-dependent regulation of TTR and Klotho gene expression. Despite being an active regulator of gene expression, APPsbeta did not rescue the lethality and neuromuscular synapse defects of APP and APLP2 double-KO animals. Our studies identify TTR and Klotho as physiological targets of APP that are regulated by soluble APPsbeta independent of developmental APP functions. This unexpected APP-mediated signaling pathway may play an important role in maintaining TTR and Klotho levels and their respective functions in Abeta sequestration and aging.
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