Evidence map›Paper›PMID 16326808›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

FGF-2 promotes neurogenesis and neuroprotection and prolongs survival in a transgenic mouse model of Huntington's disease.

Kunlin Jin, Michelle LaFevre-Bernt, Yunjuan Sun, Sylvia Chen, Juliette Gafni, Danielle Crippen, Anna Logvinova, Christopher A Ross, David A Greenberg, Lisa M Ellerby

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02704468 (FGF21 Can Help Predicting Arterial Stiffness Measured by Cardio-ankle Vascular Index in Renal Transplant Patients), which is not on this map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
6.3field-weighted citation impact, top 2% 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.

NCT02704468 completednot on this mapstarted 2016, after this paper: background citation

FGF21 Can Help Predicting Arterial Stiffness Measured by Cardio-ankle Vascular Index in Renal Transplant Patients

Typeobservational_patient_registrySponsorBangkok Metropolitan Administration Medical College and Vajira HospitalRan2016 to 2016Enrolled100ConditionsVascular StiffnessArmsCAVI and FGF-21
3 · Its place in the literature

Who cites it

83 citing papers in PubMed, 213 citations in OpenAlex.

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  14. Physical Exercise-Induced Myokines in Neurodegenerative Diseases.International journal of molecular sciences · 2021
    Review
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23 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Kunlin JinThe Buck Institute for Age Research, Novato, CA 94945, USA.
Michelle LaFevre-Bernt
Yunjuan Sun
Sylvia Chen
Juliette Gafni
Danielle Crippen
Anna Logvinova
Christopher A Ross
David A Greenberg
Lisa M Ellerby
Buck Institute for Research on Aging · USJohns Hopkins University · US

Funding

VEGF in Neurprotection and NeurogenesisR01NS044921 · NINDS · BUCK INSTITUTE FOR RESEARCH ON AGING · PI GREENBERG, DAVID ALAN · 2003 to 2013
$4.3M
Aging and NeurogenesisR01AG021980 · NIA · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI JIN, KUNLIN · 2003 to 2014
$3.9M
TRIPLET REPEAT DISEASE: REQUIREMENT FOR CASPASE CLEAVAGER01NS040251 · NINDS · BUCK INSTITUTE FOR RESEARCH ON AGING · PI ELLERBY, LISA M. · 1999 to 2007
$3.1M
Calpain in Huntington's DiseaseF32NS043937 · NINDS · BUCK INSTITUTE FOR AGE RESEARCH · PI GAFNI, JULIETTE · 2003 to 2005
$147k
Mechanism of Androgen Receptor Induced CytotoxicityF32NS043823 · NINDS · BUCK INSTITUTE FOR AGE RESEARCH · PI LAFEVRE-BERNT, MICHELLE ANNE · 2003 to 2004
$56k
NIA NIH HHS AG21980NIA NIH HHS R01 AG021980NINDS NIH HHS F32 NS043823NINDS NIH HHS F32 NS043937NINDS NIH HHS F32 NS43823NINDS NIH HHS NS40251NINDS NIH HHS NS44921NINDS NIH HHS R01 NS040251NINDS NIH HHS R01 NS044921
6 · The paper itself

Abstract

There is no satisfactory treatment for Huntington's disease (HD), a hereditary neurodegenerative disorder that produces chorea, dementia, and death. One potential treatment strategy involves the replacement of dead neurons by stimulating the proliferation of endogenous neuronal precursors (neurogenesis) and their migration into damaged regions of the brain. Because growth factors are neuroprotective in some settings and can also stimulate neurogenesis, we treated HD transgenic R6/2 mice from 8 weeks of age until death by s.c. administration of FGF-2. FGF-2 increased the number of proliferating cells in the subventricular zone by approximately 30% in wild-type mice, and by approximately 150% in HD transgenic R6/2 mice. FGF-2 also induced the recruitment of new neurons from the subventricular zone into the neostriatum and cerebral cortex of HD transgenic R6/2 mice. In the striatum, these neurons were DARPP-32-expressing medium spiny neurons, consistent with the phenotype of neurons lost in HD. FGF-2 was neuroprotective as well, because it blocked cell death induced by mutant expanded Htt in primary striatal cultures. FGF-2 also reduced polyglutamine aggregates, improved motor performance, and extended lifespan by approximately 20%. We conclude that FGF-2 improves neurological deficits and longevity in a transgenic mouse model of HD, and that its neuroprotective and neuroproliferative effects may contribute to this improvement.

Indexed as

Analysis of VarianceAnimalsBlotting, WesternBromodeoxyuridineCell DeathCell DifferentiationDopamine and cAMP-Regulated Phosphoprotein 32Fibroblast Growth Factor 2HumansHuntington DiseaseImmunohistochemistryMiceMice, TransgenicMultipotent Stem CellsNeuronsBromodeoxyuridineDopamine and cAMP-Regulated Phosphoprotein 32Fibroblast Growth Factor 2Ppp1r1b protein, mouse

Identifiers

PMID16326808
PMCPMC1312383
OpenAlexW2099819034

What OpenQuestion holds

Textmetadata
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.