Evidence map›Paper›PMID 11438588›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2001

The leukocyte common antigen-related protein tyrosine phosphatase receptor regulates regenerative neurite outgrowth in vivo.

Y Xie, T T Yeo, C Zhang, T Yang, M A Tisi, S M Massa, F M Longo

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

29 citing papers in PubMed, 75 citations in OpenAlex.

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  19. Leukocyte common antigen-related phosphatase is a functional receptor for chondroitin sulfate proteoglycan axon growth inhibitors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
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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

7 authors at 2 institutions in 1 country.

Y XieDepartment of Neurology, University of California, San Francisco/Veteran's Administration Medical Center, San Francisco, California 94121, USA.
T T Yeo
C Zhang
T Yang
M A Tisi
S M Massa
F M Longo
University of California, San Francisco · USSan Francisco VA Medical Center · US

Funding

Pediatric Scientist Development Program (PSDP) [K12]K12HD000850 · NICHD · YALE UNIVERSITY · PI Sallie R. Permar · 1987 to 2026
$44.1M
FETAL AND POSTNATAL DEVELOPMENT OF VISUAL CONNECTIONSR01EY002858 · NEI · STANFORD UNIVERSITY · PI SHATZ, CARLA J · 1985 to 2020
$9.9M
Promotion of Angiogenesis in Lung Cancer by MIFR01CA094121 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ARENBERG, DOUGLAS · 2002 to 2010
$1.9M
NOVEL LAR ISOFORMS--A NEW CLASS OF NEUTROPHIC AGENTSR01AG009873 · NIA · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI LONGO, FRANK M · 1991 to 2003
$1.2M
CORE--LABORATORYP30HD028825 · NICHD · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI LIN, DONG · 1992 to 2002
$1.0M
FETAL AND POSTNATAL DEVELOPMENT OF VISUAL CONNECTIONSR37EY002858 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI SHATZ, CARLA J · 1992 to 2001
$689k
CELLULAR BASIS FOR THALAMIC INNERVATION OF VISUAL CORTEXF32EY006602 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI DEFREITAS, MICHAEL F · 1994 to 1997
–
NCI NIH HHS R01 CA094121NEI NIH HHS EY02858NEI NIH HHS F32 EY06602NIA NIH HHS R01 AG009873NICHD NIH HHS HD28825-07NICHD NIH HHS K12HD00850
6 · The paper itself

Abstract

Drosophila and leech models of nervous system development demonstrate that protein tyrosine phosphatase (PTP) receptors regulate developmental neurite outgrowth. Whether PTP receptors regulate neurite outgrowth in adult systems or in regenerative states remains unknown. The leukocyte common antigen-related (LAR) receptor is known to be present in rodent dorsal root ganglion (DRG) neurons; therefore, the well established model of postcrush sciatic nerve regeneration was used to test the hypothesis that LAR is required for neurite outgrowth in the adult mammalian nervous system. In uninjured sciatic nerves, no differences in nerve morphology and sensory function were detected between wild-type and LAR-deficient littermate transgenic mice. Sciatic nerve crush resulted in increased LAR protein expression in DRG neurons. In addition, nerve injury led to an increase in the proportion of LAR protein isoforms known to have increased binding affinity to neurite-promoting laminin-nidogen complexes. Two weeks after nerve crush, morphological analysis of distal nerve segments in LAR-deficient transgenic mice demonstrated significantly decreased densities of myelinated fibers, decreased axonal areas, and increased myelin/axon area ratios compared with littermate controls. Electron microscopy analysis revealed a significant twofold reduction in the density of regenerating unmyelinated fibers in LAR-/- nerves distal to the crush site. Sensory testing at the 2 week time point revealed a corresponding 3 mm lag in the proximal-to-distal progression of functioning sensory fibers along the distal nerve segment. These studies introduce PTP receptors as a major new gene family regulating regenerative neurite outgrowth in vivo in the adult mammalian system.

Indexed as

Nerve RegenerationNerve Tissue ProteinsProtein Tyrosine PhosphatasesAnimalsAxonsDisease Models, AnimalGanglia, SpinalGenes, ReporterHomozygoteLamininMacromolecular SubstancesMembrane GlycoproteinsMiceMice, TransgenicNerve CrushNerve FibersLamininMacromolecular SubstancesMembrane GlycoproteinsNerve Tissue ProteinsnidogenProtein IsoformsProtein Tyrosine PhosphatasesPtprf protein, mouseReceptor-Like Protein Tyrosine Phosphatases, Class 2Receptors, Cell Surface

Identifiers

PMID11438588
PMCPMC6762843
OpenAlexW1950689805

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.