Evidence map›Paper›PMID 19326469›Full record

ArticleThe Journal of comparative neurology2009

Human neural stem cell grafts in the spinal cord of SOD1 transgenic rats: differentiation and structural integration into the segmental motor circuitry.

Leyan Xu, David K Ryugo, Tan Pongstaporn, Karl Johe, Vassilis E Koliatsos

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
6.5field-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.

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

62 citing papers in PubMed, 136 citations in OpenAlex.

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  14. Long-term Phase 1/2 intraspinal stem cell transplantation outcomes in ALS.Annals of clinical and translational neurology · 2018
    Article
  15. Current Perspectives Regarding Stem Cell-Based Therapy for Liver Cirrhosis.Canadian journal of gastroenterology & hepatology · 2018
    Review
  16. Review
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  19. Article
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2 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Leyan XuDepartment of Pathology, Division of Neuropathology, Johns Hopkins Medical Institutions, Baltimore, MD 21205, USA. lxu9@jhmi.edu
David K Ryugo
Tan Pongstaporn
Karl Johe
Vassilis E Koliatsos
Johns Hopkins University · USNeural Signals (United States) · US

Funding

Wilmer Core Grant for Vision ResearchP30EY001765 · NEI · JOHNS HOPKINS UNIVERSITY · PI Jiang Qian · 1985 to 2026
$22.1M
SINGLE-CELL MARKING STUDIES OF THE AUDITORY NERVER01DC000232 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI RYUGO, DAVID K. · 1989 to 2010
$6.4M
Models of Motor Neuron Disease: Stem Cell TherapiesR01NS045140 · NINDS · JOHNS HOPKINS UNIVERSITY · PI KOLIATSOS, VASSILIS E · 2003 to 2007
$1.7M
NCRR NIH HHS P40 RR0118604NEI NIH HHS EY01765NEI NIH HHS P30 EY001765NIDCD NIH HHS DC000232NIDCD NIH HHS R01 DC000232NINDS NIH HHS NS45140NINDS NIH HHS R01 NS045140
6 · The paper itself

Abstract

Cell replacement strategies for degenerative and traumatic diseases of the nervous system depend on the functional integration of grafted cells into host neural circuitry, a condition necessary for the propagation of physiological signals and, perhaps, targeting of trophic support to injured neurons. We have recently shown that human neural stem cell (NSC) grafts ameliorate motor neuron disease in SOD1 transgenic rodents. Here we study structural aspects of integration of neuronally differentiated human NSCs in the motor circuitry of SOD1 G93A rats. Human NSCs were grafted into the lumbar protuberance of 8-week-old SOD1 G93A rats; the results were compared to those on control Sprague-Dawley rats. Using pre-embedding immuno-electron microscopy, we found human synaptophysin (+) terminals contacting the perikarya and proximal dendrites of host alpha motor neurons. Synaptophysin (+) terminals had well-formed synaptic vesicles and were associated with membrane specializations primarily in the form of symmetrical synapses. To analyze the anatomy of motor circuits engaging differentiated NSCs, we injected the retrograde transneuronal tracer Bartha-pseudorabies virus (PRV) or the retrograde marker cholera toxin B (CTB) into the gastrocnemius muscle/sciatic nerve of SOD1 rats before disease onset and also into control rats. With this tracing, NSC-derived neurons were labeled with PRV but not CTB, a pattern suggesting that PRV entered NSC-derived neurons via transneuronal transfer from host motor neurons but not via direct transport from the host musculature. Our results indicate an advanced degree of structural integration, via functional synapses, of differentiated human NSCs into the segmental motor circuitry of SOD1-G93A rats.

Indexed as

Stem Cell TransplantationAnimalsCell DifferentiationCholera ToxinDisease Models, AnimalFemaleHumansMaleMotor Neuron DiseaseMotor NeuronsMuscle, SkeletalNeuronsRatsRats, Sprague-DawleyRats, TransgenicSciatic NerveCholera ToxinSOD1 protein, humanSod1 protein, ratSuperoxide DismutaseSuperoxide Dismutase-1Synaptophysin

Identifiers

PMID19326469
PMCPMC2727711
OpenAlexW2113360628

What OpenQuestion holds

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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.