Evidence map›Paper›PMID 26627453›Full record

ReviewCold Spring Harbor perspectives in medicine2015

The Role of the Microenvironmental Niche in Declining Stem-Cell Functions Associated with Biological Aging.

Nathan A DeCarolis, Elizabeth D Kirby, Tony Wyss-Coray, Theo D Palmer

Open access · bronzeAbstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
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  16. The individual and combined effects of spaceflight radiation and microgravity on biologic systems and functional outcomes.Journal of environmental science and health. Part C, Toxicology and carcinogenesis · 2021
    Article
  17. Review
  18. Review
  19. Loss of ARNT in skeletal muscle limits muscle regeneration in aging.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  20. The role of cofilin in age-related neuroinflammation.Neural regeneration research · 2020
    Review
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

4 authors at 3 institutions in 1 country.

Nathan A DeCarolisInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305.
Elizabeth D KirbyDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California 94305.
Tony Wyss-CorayDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California 94305 Center for Tissue Regeneration, Repair, and Restoration, Veterans Administration, Palo Alto Health Care Systems, Palo Alto, California 94304.
Theo D PalmerInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305 Department of Neurosurgery, Stanford University School of Medicine, Stanford, California 94305.
Stanford University · USCalifornia Institute for Regenerative Medicine · USVA Palo Alto Health Care System · US

Funding

Regulation and regeneration of hippocampal plasticity by neural progenitor cellsR00NS089938 · NINDS · OHIO STATE UNIVERSITY · PI KIRBY, ELIZABETH DIANA · 2017 to 2019
$747k
Regulation and regeneration of hippocampal plasticity by neural progenitor cellsK99NS089938 · NINDS · STANFORD UNIVERSITY · PI KIRBY, ELIZABETH DIANA · 2015 to 2016
$184k
NINDS NIH HHS K99 NS089938NINDS NIH HHS R00 NS089938
6 · The paper itself

Abstract

Aging is strongly correlated with decreases in neurogenesis, the process by which neural stem and progenitor cells proliferate and differentiate into new neurons. In addition to stem-cell-intrinsic factors that change within the aging stem-cell pool, recent evidence emphasizes new roles for systemic and microenvironmental factors in modulating the neurogenic niche. This article focuses on new insights gained through the use of heterochronic parabiosis models, in which an old mouse and a young circulatory system are joined. By studying the brains of both young and old mice, researchers are beginning to uncover circulating proneurogenic "youthful" factors and "aging" factors that decrease stem-cell activity and neurogenesis. Ultimately, the identification of factors that influence stem-cell aging may lead to strategies that slow or even reverse age-related decreases in neural-stem-cell (NSC) function and neurogenesis.

Indexed as

AgingAnimalsBrainCell ProliferationHumansMiceNeural Stem CellsNeurogenesisNeuronsParabiosisStem Cell Niche

Identifiers

PMID26627453
PMCPMC4665032
OpenAlexW2259248206

What OpenQuestion holds

Textmetadata
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.