TY - JOUR
T1 - Organization of the Mammalian Ionome According to Organ Origin, Lineage Specialization, and Longevity
AU - Ma, Siming
AU - Lee, Sang Goo
AU - Kim, Eun Bae
AU - Park, Thomas J.
AU - Seluanov, Andrei
AU - Gorbunova, Vera
AU - Buffenstein, Rochelle
AU - Seravalli, Javier
AU - Gladyshev, Vadim N.
N1 - Funding Information:
This work was supported by NIH AG047745, AG047200, CA080946, and GM061603 as well as the WCU Program R31-2008-000-10010-0 and Life Extension Foundation. We thank Anton Turanov and Sun Hee Yim for help with sample collection or preparation.
Publisher Copyright:
© 2015 The Authors.
PY - 2015/11/17
Y1 - 2015/11/17
N2 - Trace elements are essential to all mammals, but their distribution and utilization across species and organs remains unclear. Here, we examined 18 elements in the brain, heart, kidney, and liver of 26 mammalian species and report the elemental composition of these organs, the patterns of utilization across the species, and their correlation with body mass and longevity. Across the organs, we observed distinct distribution patterns for abundant elements, transition metals, and toxic elements. Some elements showed lineage-specific patterns, including reduced selenium utilization in African mole rats, and positive correlation between the number of selenocysteine residues in selenoprotein P and the selenium levels in liver and kidney across mammals. Body mass was linked positively to zinc levels, whereas species lifespan correlated positively with cadmium and negatively with selenium. This study provides insights into the variation of mammalian ionome by organ physiology, lineage specialization, body mass, and longevity.
AB - Trace elements are essential to all mammals, but their distribution and utilization across species and organs remains unclear. Here, we examined 18 elements in the brain, heart, kidney, and liver of 26 mammalian species and report the elemental composition of these organs, the patterns of utilization across the species, and their correlation with body mass and longevity. Across the organs, we observed distinct distribution patterns for abundant elements, transition metals, and toxic elements. Some elements showed lineage-specific patterns, including reduced selenium utilization in African mole rats, and positive correlation between the number of selenocysteine residues in selenoprotein P and the selenium levels in liver and kidney across mammals. Body mass was linked positively to zinc levels, whereas species lifespan correlated positively with cadmium and negatively with selenium. This study provides insights into the variation of mammalian ionome by organ physiology, lineage specialization, body mass, and longevity.
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U2 - 10.1016/j.celrep.2015.10.014
DO - 10.1016/j.celrep.2015.10.014
M3 - Article
C2 - 26549444
AN - SCOPUS:84947341093
SN - 2211-1247
VL - 13
SP - 1319
EP - 1326
JO - Cell Reports
JF - Cell Reports
IS - 7
ER -