ArticlebioRxiv : the preprint server for biology2024
Late-life dietary folate restriction reduces biosynthetic processes without compromising healthspan in mice.
Heidi M Blank, Staci E Hammer, Laurel Boatright, Courtney Roberts, Katarina E Heyden, Aravindh Nagarajan, Mitsuhiro Tsuchiya, Marcel Brun, Charles D Johnson, Patrick J Stover and 8 more
Open access · greenAbstract readPreprint
In one paragraphArticle in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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0citing papers in PubMed
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1 · What the graph read from itWhat it found
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2 · The registryThe trial behind it
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3 · Its place in the literatureWho cites it
0 citing papers in PubMed, 0 citations in OpenAlex.
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4 · The recordCorrections and comments
5 · Who and what moneyAuthors and funding
18 authors at 6 institutions in 2 countries.
Heidi M BlankDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0002-2251-5246 Staci E HammerDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0001-5874-5521 Laurel BoatrightDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.
Courtney RobertsDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.
Katarina E HeydenDivision of Nutritional Sciences, Cornell University, Ithaca, United States.
Aravindh NagarajanDepartment of Microbial Pathogenesis and Immunology, School of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID 0000-0001-9613-3729 Mitsuhiro TsuchiyaDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, United States.
Marcel BrunTexas A&M Agrilife Research, Genomics and Bioinformatics Service, College Station, United States.ORCID 0000-0002-6452-5856 Charles D JohnsonTexas A&M Agrilife Research, Genomics and Bioinformatics Service, College Station, United States.
Patrick J StoverDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0002-7546-3814 Raquel SitcheranDepartment of Cell Biology and Genetics, School of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID 0000-0001-8916-9707 Brian K KennedyDepartments of Biochemistry and Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID 0000-0002-5754-1874 L Garry AdamsDepartment of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M, College Station, Texas, USA.ORCID 0000-0002-7246-1602 Matt KaeberleinDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, United States.ORCID 0000-0002-1311-3421 David W ThreadgillDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0003-3538-1635 Helene L Andrews-PolymenisDepartment of Microbial Pathogenesis and Immunology, School of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID 0000-0002-1818-1335 Michael PolymenisDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0003-1507-0936 Texas A&M Health Science Center · USTexas A&M University · USCenter for Advancing Health · USCornell University · USUniversity of Washington · USNational University of Singapore · SG
Funding
Coupling Of Protein Synthesis With Cell DivisionR01GM123139 · NIGMS · TEXAS A&M AGRILIFE RESEARCH · PI POLYMENIS, MICHAEL S · 2017 to 2024
$2.9MType I Interferon Responses in the Pathobiology of Anthracycline-induced CardiotoxicityR01HL148153 · NHLBI · TEXAS A&M UNIVERSITY · PI John Travis Hinson, Andrew Phillip West · 2020 to 2026
$2.8MElucidating the Bacterial and Host Mechanisms Governing B. burgdorferi-Related Type I Interferon ResponsesR21AI153879 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI HYDE, JENNY A. · 2021 to 2022
$409kNHLBI NIH HHS R01 HL148153NIAID NIH HHS R21 AI153879NIGMS NIH HHS R01 GM123139
6 · The paper itselfAbstract
Folate is a vitamin required for cell growth and is present in fortified foods in the form of folic acid to prevent congenital abnormalities. The impact of low folate status on life-long health is poorly understood. We found that limiting folate levels with the folate antagonist methotrexate increased the lifespan of yeast and worms. We then restricted folate intake in aged mice and measured various health metrics, metabolites, and gene expression signatures. Limiting folate intake decreased anabolic biosynthetic processes in mice and enhanced metabolic plasticity. Despite reduced serum folate levels in mice with limited folic acid intake, these animals maintained their weight and adiposity late in life, and we did not observe adverse health outcomes. These results argue that the effectiveness of folate dietary interventions may vary depending on an individual's age and sex. A higher folate intake is advantageous during the early stages of life to support cell divisions needed for proper development. However, a lower folate intake later in life may result in healthier aging.
Identifiers
PMID38260683
PMCPMC10802571
OpenAlexW4390813055
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