Effects of Sex, Strain, and Energy Intake on Hallmarks of Aging in Mice

Sarah J. Mitchell; Julio Madrigal-Matute; Morten Scheibye-Knudsen; Evandro Fang; Miguel Aon; José A. González-Reyes; Sonia Cortassa; Susmita Kaushik; Marta Gonzalez-Freire; Bindi Patel; Devin Wahl; Ahmed Ali; Miguel Calvo-Rubio; María I. Burón; Vincent Guiterrez; Theresa M. Ward; Hector H. Palacios; Huan Cai; David W. Frederick; Christopher Hine; Filomena Broeskamp; Lukas Habering; John Dawson; T. Mark Beasley; Junxiang Wan; Yuji Ikeno; Gene Hubbard; Kevin G. Becker; Yongqing Zhang; Vilhelm A. Bohr; Dan L. Longo; Placido Navas; Luigi Ferrucci; David A. Sinclair; Pinchas Cohen; Josephine M. Egan; James R. Mitchell; Joseph A. Baur; David B. Allison; R. Michael Anson; José M. Villalba; Frank Madeo; Ana Maria Cuervo; Kevin J. Pearson; Donald K. Ingram; Michel Bernier; Rafael De Cabo

doi:10.1016/j.cmet.2016.05.027

Effects of Sex, Strain, and Energy Intake on Hallmarks of Aging in Mice

Sarah J. Mitchell
, Julio Madrigal-Matute
, Morten Scheibye-Knudsen
, Evandro Fang
, Miguel Aon
, José A. González-Reyes
, Sonia Cortassa
, Susmita Kaushik
, Marta Gonzalez-Freire
, Bindi Patel
, Devin Wahl
, Ahmed Ali
, Miguel Calvo-Rubio
, María I. Burón
, Vincent Guiterrez
, Theresa M. Ward
, Hector H. Palacios
, Huan Cai
, David W. Frederick
, Christopher Hine

Filomena Broeskamp, Lukas Habering, John Dawson, T. Mark Beasley, Junxiang Wan, Yuji Ikeno, Gene Hubbard, Kevin G. Becker, Yongqing Zhang, Vilhelm A. Bohr, Dan L. Longo, Placido Navas, Luigi Ferrucci, David A. Sinclair, Pinchas Cohen, Josephine M. Egan, James R. Mitchell, Joseph A. Baur, David B. Allison, R. Michael Anson, José M. Villalba, Frank Madeo, Ana Maria Cuervo, Kevin J. Pearson, Donald K. Ingram, Michel Bernier, Rafael De Cabo

Producción científica: Article › revisión exhaustiva

393 Citas (Scopus)

Resumen

Calorie restriction (CR) is the most robust non-genetic intervention to delay aging. However, there are a number of emerging experimental variables that alter CR responses. We investigated the role of sex, strain, and level of CR on health and survival in mice. CR did not always correlate with lifespan extension, although it consistently improved health across strains and sexes. Transcriptional and metabolomics changes driven by CR in liver indicated anaplerotic filling of the Krebs cycle together with fatty acid fueling of mitochondria. CR prevented age-associated decline in the liver proteostasis network while increasing mitochondrial number, preserving mitochondrial ultrastructure and function with age. Abrogation of mitochondrial function negated life-prolonging effects of CR in yeast and worms. Our data illustrate the complexity of CR in the context of aging, with a clear separation of outcomes related to health and survival, highlighting complexities of translation of CR into human interventions.

Idioma original	English
Páginas (desde-hasta)	1093-1112
Número de páginas	20
Publicación	Cell Metabolism
Volumen	23
N.º	6
DOI	https://doi.org/10.1016/j.cmet.2016.05.027
Estado	Published - jun 14 2016

Nota bibliográfica

Publisher Copyright:
© 2016 Published by Elsevier Inc.

Financiación

This work was supported in part by the Intramural Research Program of the National Institute on Aging, NIH, and by NIH grants R01 AG043483 and R01 DK098656 (J.A.B.), NIH grant AG031782 (A.M.C.), and the Proteostasis of Aging Core AG038072 (A.M.C.). J.M.M. was supported by a postdoctoral fellowship from the American Diabetes Association, grant 1-15-MI-03. P.C. was supported by NIH grants (1P01AG034906, 1R01GM090311, and 1R01ES 020812). F.M. is grateful to the FWF for grants LIPOTOX, I1000, P27893, P29203, and P24381-B20 and the BMWFW for grants “Unconventional Research” and “Flysleep” (80.109/0001-WF/V/3b/2015). J.M.V. was supported by the Spanish Ministerio de Economía y Competitividad (grants BFU2011-23578 and BFU2015-64630-R). The authors thank the personnel from the Servicio Centralizado de Apoyo a la Investigación (SCAI; University of Córdoba) for technical support. Special thanks to the members of the Translational Gerontology Branch and the Comparative Medicine Section of the National Institute on Aging. In particular we acknowledge Paul Bastian, Elin Lehrmann, Frances Fan, Robin Minor, Dawn Nines, and Dawn Boyer.

Financiadores	Número del financiador
Proteostasis of Aging Core	AG038072
National Institutes of Health (NIH)	R01 DK098656, R01 AG043483
National Institutes of Health (NIH)
American Diabetes Association Inc	1R01GM090311, 1-15-MI-03, 1P01AG034906, 1R01ES 020812
American Diabetes Association Inc
National Institute on Aging	P01AG031782
National Institute on Aging
Austrian Science Fund/FWF	P29203, I1000, P27893, P24381-B20
Austrian Science Fund/FWF
Ministerio de Economía y Competitividad	BFU2011-23578, BFU2015-64630-R
Ministerio de Economía y Competitividad
Bundesministerium für Wissenschaft, Forschung und Wirtschaft	80.109/0001-WF/V/3b/2015
Bundesministerium für Wissenschaft, Forschung und Wirtschaft

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

Good health and well being

ASJC Scopus subject areas

Physiology
Molecular Biology
Cell Biology

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10.1016/j.cmet.2016.05.027

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Mitchell, S. J., Madrigal-Matute, J., Scheibye-Knudsen, M., Fang, E., Aon, M., González-Reyes, J. A., Cortassa, S., Kaushik, S., Gonzalez-Freire, M., Patel, B., Wahl, D., Ali, A., Calvo-Rubio, M., Burón, M. I., Guiterrez, V., Ward, T. M., Palacios, H. H., Cai, H., Frederick, D. W., ... De Cabo, R. (2016). Effects of Sex, Strain, and Energy Intake on Hallmarks of Aging in Mice. Cell Metabolism, 23(6), 1093-1112. https://doi.org/10.1016/j.cmet.2016.05.027

@article{f62edf6d1a104c2a873b0fa7deca87ec,

title = "Effects of Sex, Strain, and Energy Intake on Hallmarks of Aging in Mice",

abstract = "Calorie restriction (CR) is the most robust non-genetic intervention to delay aging. However, there are a number of emerging experimental variables that alter CR responses. We investigated the role of sex, strain, and level of CR on health and survival in mice. CR did not always correlate with lifespan extension, although it consistently improved health across strains and sexes. Transcriptional and metabolomics changes driven by CR in liver indicated anaplerotic filling of the Krebs cycle together with fatty acid fueling of mitochondria. CR prevented age-associated decline in the liver proteostasis network while increasing mitochondrial number, preserving mitochondrial ultrastructure and function with age. Abrogation of mitochondrial function negated life-prolonging effects of CR in yeast and worms. Our data illustrate the complexity of CR in the context of aging, with a clear separation of outcomes related to health and survival, highlighting complexities of translation of CR into human interventions.",

author = "Mitchell, \{Sarah J.\} and Julio Madrigal-Matute and Morten Scheibye-Knudsen and Evandro Fang and Miguel Aon and Gonz{\'a}lez-Reyes, \{Jos{\'e} A.\} and Sonia Cortassa and Susmita Kaushik and Marta Gonzalez-Freire and Bindi Patel and Devin Wahl and Ahmed Ali and Miguel Calvo-Rubio and Bur{\'o}n, \{Mar{\'i}a I.\} and Vincent Guiterrez and Ward, \{Theresa M.\} and Palacios, \{Hector H.\} and Huan Cai and Frederick, \{David W.\} and Christopher Hine and Filomena Broeskamp and Lukas Habering and John Dawson and Beasley, \{T. Mark\} and Junxiang Wan and Yuji Ikeno and Gene Hubbard and Becker, \{Kevin G.\} and Yongqing Zhang and Bohr, \{Vilhelm A.\} and Longo, \{Dan L.\} and Placido Navas and Luigi Ferrucci and Sinclair, \{David A.\} and Pinchas Cohen and Egan, \{Josephine M.\} and Mitchell, \{James R.\} and Baur, \{Joseph A.\} and Allison, \{David B.\} and Anson, \{R. Michael\} and Villalba, \{Jos{\'e} M.\} and Frank Madeo and Cuervo, \{Ana Maria\} and Pearson, \{Kevin J.\} and Ingram, \{Donald K.\} and Michel Bernier and \{De Cabo\}, Rafael",

note = "Publisher Copyright: {\textcopyright} 2016 Published by Elsevier Inc.",

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Mitchell, SJ, Madrigal-Matute, J, Scheibye-Knudsen, M, Fang, E, Aon, M, González-Reyes, JA, Cortassa, S, Kaushik, S, Gonzalez-Freire, M, Patel, B, Wahl, D, Ali, A, Calvo-Rubio, M, Burón, MI, Guiterrez, V, Ward, TM, Palacios, HH, Cai, H, Frederick, DW, Hine, C, Broeskamp, F, Habering, L, Dawson, J, Beasley, TM, Wan, J, Ikeno, Y, Hubbard, G, Becker, KG, Zhang, Y, Bohr, VA, Longo, DL, Navas, P, Ferrucci, L, Sinclair, DA, Cohen, P, Egan, JM, Mitchell, JR, Baur, JA, Allison, DB, Anson, RM, Villalba, JM, Madeo, F, Cuervo, AM, Pearson, KJ, Ingram, DK, Bernier, M & De Cabo, R 2016, 'Effects of Sex, Strain, and Energy Intake on Hallmarks of Aging in Mice', Cell Metabolism, vol. 23, n.º 6, pp. 1093-1112. https://doi.org/10.1016/j.cmet.2016.05.027

TY - JOUR

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AU - Mitchell, Sarah J.

AU - Madrigal-Matute, Julio

AU - Scheibye-Knudsen, Morten

AU - Fang, Evandro

AU - Aon, Miguel

AU - González-Reyes, José A.

AU - Cortassa, Sonia

AU - Kaushik, Susmita

AU - Gonzalez-Freire, Marta

AU - Patel, Bindi

AU - Wahl, Devin

AU - Ali, Ahmed

AU - Calvo-Rubio, Miguel

AU - Burón, María I.

AU - Guiterrez, Vincent

AU - Ward, Theresa M.

AU - Palacios, Hector H.

AU - Cai, Huan

AU - Frederick, David W.

AU - Hine, Christopher

AU - Broeskamp, Filomena

AU - Habering, Lukas

AU - Dawson, John

AU - Beasley, T. Mark

AU - Wan, Junxiang

AU - Ikeno, Yuji

AU - Hubbard, Gene

AU - Becker, Kevin G.

AU - Zhang, Yongqing

AU - Bohr, Vilhelm A.

AU - Longo, Dan L.

AU - Navas, Placido

AU - Ferrucci, Luigi

AU - Sinclair, David A.

AU - Cohen, Pinchas

AU - Egan, Josephine M.

AU - Mitchell, James R.

AU - Baur, Joseph A.

AU - Allison, David B.

AU - Anson, R. Michael

AU - Villalba, José M.

AU - Madeo, Frank

AU - Cuervo, Ana Maria

AU - Pearson, Kevin J.

AU - Ingram, Donald K.

AU - Bernier, Michel

AU - De Cabo, Rafael

PY - 2016/6/14

Y1 - 2016/6/14

N2 - Calorie restriction (CR) is the most robust non-genetic intervention to delay aging. However, there are a number of emerging experimental variables that alter CR responses. We investigated the role of sex, strain, and level of CR on health and survival in mice. CR did not always correlate with lifespan extension, although it consistently improved health across strains and sexes. Transcriptional and metabolomics changes driven by CR in liver indicated anaplerotic filling of the Krebs cycle together with fatty acid fueling of mitochondria. CR prevented age-associated decline in the liver proteostasis network while increasing mitochondrial number, preserving mitochondrial ultrastructure and function with age. Abrogation of mitochondrial function negated life-prolonging effects of CR in yeast and worms. Our data illustrate the complexity of CR in the context of aging, with a clear separation of outcomes related to health and survival, highlighting complexities of translation of CR into human interventions.

AB - Calorie restriction (CR) is the most robust non-genetic intervention to delay aging. However, there are a number of emerging experimental variables that alter CR responses. We investigated the role of sex, strain, and level of CR on health and survival in mice. CR did not always correlate with lifespan extension, although it consistently improved health across strains and sexes. Transcriptional and metabolomics changes driven by CR in liver indicated anaplerotic filling of the Krebs cycle together with fatty acid fueling of mitochondria. CR prevented age-associated decline in the liver proteostasis network while increasing mitochondrial number, preserving mitochondrial ultrastructure and function with age. Abrogation of mitochondrial function negated life-prolonging effects of CR in yeast and worms. Our data illustrate the complexity of CR in the context of aging, with a clear separation of outcomes related to health and survival, highlighting complexities of translation of CR into human interventions.

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DO - 10.1016/j.cmet.2016.05.027

M3 - Article

C2 - 27304509

AN - SCOPUS:84975455180

SN - 1550-4131

VL - 23

SP - 1093

EP - 1112

JO - Cell Metabolism

JF - Cell Metabolism

IS - 6

ER -

Effects of Sex, Strain, and Energy Intake on Hallmarks of Aging in Mice

Resumen

Nota bibliográfica

Financiación

ODS de las Naciones Unidas

ASJC Scopus subject areas

Acceder al documento

Otros archivos y enlaces

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