Title
Increased expression of ApoE and protection from amyloid-beta toxicity in transmitochondrial cybrids with haplogroup K mtDNA
Date Issued
01 September 2016
Access level
open access
Resource Type
journal article
Author(s)
Thaker K.
Chwa M.
Atilano S.
Coskun P.
Udar N.
Boyer D.
Jazwinski S.
Miceli M.
Nesburn A.
Kuppermann B.
Kenney M.
University of California Irvine
Publisher(s)
Academic Press Inc.
Abstract
Mitochondrial (mt) DNA haplogroups, defined by specific single nucleotide polymorphism (SNP) patterns, represent populations of diverse geographic origins and have been associated with increased risk or protection of many diseases. The H haplogroup is the most common European haplogroup while the K haplogroup is highly associated with the Ashkenazi Jewish population. Transmitochondrial cybrids (cell lines with identical nuclei, but mtDNA from either H (n = 8) or K (n = 8) subjects) were analyzed by the Seahorse flux analyzer, quantitative polymerase chain reaction (Q-PCR) and immunohistochemistry (IHC). Cybrids were treated with amyloid-β peptides and cell viabilities were measured. Other cybrids were demethylated with 5-aza-2'-deoxycytidine (5-aza-dC) and expression levels for APOE and NFkB2 were measured. Results show K cybrids have (a) significantly lower mtDNA copy numbers, (b) higher expression levels for MT-DNA encoded genes critical for oxidative phosphorylation, (c) lower Spare Respiratory Capacity, (d) increased expression of inhibitors of the complement pathway and important inflammasome-related genes; and (e) significantly higher levels of APOE transcription that were independent of methylation status. After exposure to amyloid-β1-42 peptides (active form), H haplogroup cybrids demonstrated decreased cell viability compared to those treated with amyloid-β42-1 (inactive form) (p < 0.0001), while this was not observed in the K cybrids (p = 0.2). K cybrids had significantly higher total global methylation levels and differences in expression levels for two acetylation genes and four methylation genes. Demethylation with 5-aza-dC altered expression levels for NFkB2, while APOE transcription patterns were unchanged. Our findings support the hypothesis that mtDNA-nuclear retrograde signaling may mediate expression levels of APOE, a key factor in many age-related diseases. Future studies will focus on identification of the mitochondrial-nuclear retrograde signaling mechanism(s) contributing to these mtDNA-mediated differences.
Start page
64
End page
77
Volume
93
Language
English
OCDE Knowledge area
Genética, Herencia
BioquÃmica, BiologÃa molecular
Scopus EID
2-s2.0-84966701389
PubMed ID
Source
Neurobiology of Disease
ISSN of the container
09699961
Sponsor(s)
This work was supported by the Discovery Eye Foundation, Polly and Michael Smith Foundation, Iris and the B. Gerald Cantor Foundation, Beckman Initiative for Macular Research, Max Factor Family Foundation, Lincy Foundation, Guenther Foundation, and the National Institute on Aging [AG006168 to SMJ]. We acknowledge the support of the Institute for Clinical and Translational Science (ICTS) at University of California Irvine.
Sources of information:
Directorio de Producción CientÃfica
Scopus