Evidence map›Paper›PMID 29124393›Full record

ReviewCell and tissue research2018

The systemic environment: at the interface of aging and adult neurogenesis.

Lucas K Smith, Charles W White, Saul A Villeda

Open access · hybridAbstract readReview
In one paragraph

Review in Cell and tissue research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.6field-weighted citation impact, top 4% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 68 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Lucas K SmithDepartment of Anatomy, University of California, San Francisco, San Francisco, CA, 94143, USA.
Charles W WhiteDepartment of Anatomy, University of California, San Francisco, San Francisco, CA, 94143, USA.
Saul A VilledaDepartment of Anatomy, University of California, San Francisco, San Francisco, CA, 94143, USA. saul.villeda@ucsf.edu.
University of California, San Francisco · USBroad Center · US

Funding

PREDOCTORAL TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007470 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Todd Nystul · 1994 to 2026
$7.7M
PREDOCTORAL TRAINING IN BIOMEDICAL SCIENCEST32GM008568 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANSEL, KARL MARK · 1995 to 2019
$6.3M
Mechanisms of brain rejuvenationR01AG053382 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VILLEDA, SAUL A · 2016 to 2020
$2.0M
Regulation of Neurogenesis and Cognition by Systemic Age-Related Immune FactorsDP5OD012178 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VILLEDA, SAUL A · 2012 to 2016
$1.8M
Investigating the pro-aging role of B2M and MHC molecules on regenerative and cognitive function in the brainR01AG055797 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VILLEDA, SAUL A · 2017 to 2021
$1.6M
NIA NIH HHS R01 AG053382NIA NIH HHS R01 AG055797NIA NIH HHS R01-AG055797NICHD NIH HHS T32 HD007470NIGMS NIH HHS T32 GM008568NIH HHS DP5 OD012178
6 · The paper itself

Abstract

Aging results in impaired neurogenesis in the two neurogenic niches of the adult mammalian brain, the dentate gyrus of the hippocampus and the subventricular zone of the lateral ventricle. While significant work has characterized intrinsic cellular changes that contribute to this decline, it is increasingly apparent that the systemic environment also represents a critical driver of brain aging. Indeed, emerging studies utilizing the model of heterochronic parabiosis have revealed that immune-related molecular and cellular changes in the aging systemic environment negatively regulate adult neurogenesis. Interestingly, these studies have also demonstrated that age-related decline in neurogenesis can be ameliorated by exposure to the young systemic environment. While this burgeoning field of research is increasingly garnering interest, as yet, the precise mechanisms driving either the pro-aging effects of aged blood or the rejuvenating effects of young blood remain to be thoroughly defined. Here, we review how age-related changes in blood, blood-borne factors, and peripheral immune cells contribute to the age-related decline in adult neurogenesis in the mammalian brain, and posit both direct neural stem cell and indirect neurogenic niche-mediated mechanisms.

Indexed as

AdultAgingAnimalsBloodHippocampusHumansLateral VentriclesLeukocytesMiceModels, AnimalNeurogenesisNeuronsParabiosisRatsAdult neurogenesisAgingBloodImmune cellsRejuvenation

Identifiers

PMID29124393
PMCPMC5748432
OpenAlexW2767820867

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.