Evidence map›Paper›PMID 21886162›Full record

ArticleNature2011

The ageing systemic milieu negatively regulates neurogenesis and cognitive function.

Saul A Villeda, Jian Luo, Kira I Mosher, Bende Zou, Markus Britschgi, Gregor Bieri, Trisha M Stan, Nina Fainberg, Zhaoqing Ding, Alexander Eggel and 13 more

4 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Nature, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 1,072 papers.

0numbers the graph read from it
0cells of the map it votes in
1,072citing papers in PubMed
37.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02460731 phase1completednot on this mapstarted 2015, after this paper: background citation

A 6 Month, Open-Label, Pilot Futility Clinical Trial of Monthly Young Healthy Male Donor Plasma Transfusions for Progressive Supranuclear Palsy

TypeinterventionalSponsorUniversity of California, San FranciscoRan2015 to 2019Enrolled6ConditionsProgressive Supranuclear PalsyArmsFresh Frozen Plasma
NCT02968433 phase1completednot on this mapstarted 2016, after this paper: background citation

The Stanford Parkinson's Disease Plasma (SPDP) Study: Intravenously-Administered Plasma From Young Donors for Treatment of Moderate Parkinson's Disease

TypeinterventionalSponsorStanford UniversityRan2016 to 2019Enrolled16ConditionsParkinson Disease(PD)ArmsInfusions of young plasma
NCT03353597 phase1 / phase2unknown statusnot on this mapstarted 2018, after this paper: background citation

Reversing Epigenetic & Other Markers of Senescence by Transfusing Young Plasma To Older Human Subjects

TypeinterventionalSponsorChandra DuggiralaRan2018 to 2022Enrolled2,120ConditionsAgingArmsPlasma Transfusion
NCT04566757 phase1unknown statusnot on this mapstarted 2021, after this paper: background citation

Safety and Efficacy of Human Umbilical Cord Blood Plasma Infusion for Age-Related Cognitive Decline

TypeinterventionalSponsorAmerican Academy of Regenerative MedicineRan2021 to 2022Enrolled12ConditionsAge-related Cognitive DeclineArmsUmbilical Cord Blood Plasma
3 · Its place in the literature

Who cites it

1,072 citing papers in PubMed, 1,737 citations in OpenAlex.

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1,012 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 9 institutions in 3 countries.

Saul A VilledaDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California 94305, USA.
Jian Luo
Kira I Mosher
Bende Zou
Markus Britschgi
Gregor Bieri
Trisha M Stan
Nina Fainberg
Zhaoqing Ding
Alexander Eggel
Kurt M Lucin
Eva Czirr
Jeong-Soo Park
Sebastien Couillard-Després
Ludwig Aigner
Ge Li
Elaine R Peskind
Jeffrey A Kaye
Joseph F Quinn
Douglas R Galasko
Xinmin S Xie
Thomas A Rando
Tony Wyss-Coray
Stanford University · USCACI International (United States) · USParacelsus Medical University · ATOregon Health & Science University · USPortland VA Medical Center · USUniversity of California, San Diego · USUniversity of Washington · USVA Northwest Network · USVA Palo Alto Health Care System · US

Funding

THERAPEUTIC EFFECTS OF INTRA-NASAL INSULIN DETEMIRP50AG005136 · NIA · UNIVERSITY OF WASHINGTON · PI JAYADEY, SUMAN · 1985 to 2019
$57.2M
Outreach, Recruitment and Education CoreP30AG008017 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI KAYE, JEFFREY A · 1990 to 2019
$27.7M
MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
NIH Director's Pioneer Award (RMI)DP1OD000392 · OD · STANFORD UNIVERSITY · PI RANDO, THOMAS A. · 2005 to 2009
$3.3M
Molecular Regulation of Myogenic DifferentiationR01AR056849 · NIAMS · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI RANDO, THOMAS A. · 2009 to 2013
$1.5M
TGFbeta signaling in neurodegeneration and Alzhimer'sR01AG027505 · NIA · STANFORD UNIVERSITY · PI WYSS-CORAY, TONY · 2006 to 2010
$1.3M
Modulation of Nociceptin/Orphanin FQ on Hypocretin Neurons in Pain and StressR01MH078194 · NIMH · AFASCI, INC. · PI XIE, XINMIN SIMON · 2008 to 2011
$1.3M
Regulation of Neural Stem Cells by Changes in the Aging Systemic EnvironmentF31AG034045 · NIA · STANFORD UNIVERSITY · PI VILLEDA, SAUL A · 2009 to 2011
$88k
Role of Microglia Proliferation in Experimental Autoimmune EncephalomyelitisF31NS066676 · NINDS · STANFORD UNIVERSITY · PI DING, ZHAOQING · 2010 to 2011
$64k
NIAID NIH HHS T32 AI007290NIAMS NIH HHS R01 AR056849NIA NIH HHS 1 F31 AG034045-01NIA NIH HHS F31 AG034045NIA NIH HHS P30 AG008017NIA NIH HHS P30AG08017NIA NIH HHS P50 AG005136NIA NIH HHS R01 AG027505NIA NIH HHS R01AG027505NIH HHS DP1 OD000392NIMH NIH HHS R01 MH078194NINDS NIH HHS 1 F31 NS066676-01A1NINDS NIH HHS F31 NS066676
6 · The paper itself

Abstract

In the central nervous system, ageing results in a precipitous decline in adult neural stem/progenitor cells and neurogenesis, with concomitant impairments in cognitive functions. Interestingly, such impairments can be ameliorated through systemic perturbations such as exercise. Here, using heterochronic parabiosis we show that blood-borne factors present in the systemic milieu can inhibit or promote adult neurogenesis in an age-dependent fashion in mice. Accordingly, exposing a young mouse to an old systemic environment or to plasma from old mice decreased synaptic plasticity, and impaired contextual fear conditioning and spatial learning and memory. We identify chemokines--including CCL11 (also known as eotaxin)--the plasma levels of which correlate with reduced neurogenesis in heterochronic parabionts and aged mice, and the levels of which are increased in the plasma and cerebrospinal fluid of healthy ageing humans. Lastly, increasing peripheral CCL11 chemokine levels in vivo in young mice decreased adult neurogenesis and impaired learning and memory. Together our data indicate that the decline in neurogenesis and cognitive impairments observed during ageing can be in part attributed to changes in blood-borne factors.

Indexed as

AgingAnimalsChemokine CCL11ChemokinesFemaleLearningLearning DisabilitiesMaleMemory DisordersMiceMice, Inbred C57BLNeurogenesisParabiosisPlasmaTime FactorsChemokine CCL11Chemokines

Identifiers

PMID21886162
PMCPMC3170097
OpenAlexW1969905245

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.