TY - JOUR
T1 - Generation and characterization of two human induced pluripotent stem cell (hiPSC) lines homozygous for the Apolipoprotein e4 (APOE4) risk variant—Alzheimer's disease (ASUi005-A) and healthy non-demented control (ASUi006-A)
AU - Brookhouser, Nicholas
AU - Zhang, Ping
AU - Caselli, Richard
AU - Kim, Jean J.
AU - Brafman, David
N1 - Funding Information:
This work was supported by the NIH ( 5R21AG056706-02 ), an ASU-Mayo Seed Grant ( FP00004591 ) and the Arizona Alzheimer's Disease Consortium .
Publisher Copyright:
© 2018 The Authors
PY - 2018/10
Y1 - 2018/10
N2 - Although the majority of late-onset Alzheimer's disease (AD) patients are labeled sporadic, multiple genetic risk variants have been identified, the most powerful and prevalent of which is the e4 variant of the Apolipoprotein E (APOE) gene. Here, we generated human induced pluripotent stem cell (hiPSC) lines from the peripheral blood mononuclear cells (PBMCs) of a clinically diagnosed AD patient [ASUi005-A] and a non-demented control (NDC) patient [ASUi006-A] homozygous for the APOE4 risk allele. These hiPSCs maintained their original genotype, expressed pluripotency markers, exhibited a normal karyotype, and retained the ability to differentiate into cells representative of the three germ layers.
AB - Although the majority of late-onset Alzheimer's disease (AD) patients are labeled sporadic, multiple genetic risk variants have been identified, the most powerful and prevalent of which is the e4 variant of the Apolipoprotein E (APOE) gene. Here, we generated human induced pluripotent stem cell (hiPSC) lines from the peripheral blood mononuclear cells (PBMCs) of a clinically diagnosed AD patient [ASUi005-A] and a non-demented control (NDC) patient [ASUi006-A] homozygous for the APOE4 risk allele. These hiPSCs maintained their original genotype, expressed pluripotency markers, exhibited a normal karyotype, and retained the ability to differentiate into cells representative of the three germ layers.
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U2 - 10.1016/j.scr.2018.09.007
DO - 10.1016/j.scr.2018.09.007
M3 - Article
C2 - 30296667
AN - SCOPUS:85054253314
SN - 1873-5061
VL - 32
SP - 145
EP - 149
JO - Stem Cell Research
JF - Stem Cell Research
ER -