Evidence map›Paper›PMID 17182780›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2006

Primary afferent synapses on developing and adult Renshaw cells.

George Z Mentis, Valerie C Siembab, Ricardo Zerda, Michael J O'Donovan, Francisco J Alvarez

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

54 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
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  8. Structural Preservation Does Not Ensure Function at Sensory Ia-Motoneuron Synapses following Peripheral Nerve Injury and Repair.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  9. Article
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  13. Spinal Inhibitory Interneurons: Gatekeepers of Sensorimotor Pathways.International journal of molecular sciences · 2021
    Review
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  15. Review
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  17. Review
  18. Characterization of calbindin D28k expressing interneurons in the ventral horn of the mouse spinal cord.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    Article
  19. Article
  20. Descending Systems Direct Development of Key Spinal Motor Circuits.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
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.

George Z MentisLaboratory of Neural Control, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.
Valerie C Siembab
Ricardo Zerda
Michael J O'Donovan
Francisco J Alvarez
Wright State University · USNational Institute of Neurological Disorders and Stroke · US

Funding

DEVELOPMENT OF SYNAPTIC INPUTS ON SPINAL INTERNEURONSR01NS047357 · NINDS · WRIGHT STATE UNIVERSITY · PI ALVAREZ, FRANCISCO J · 2004 to 2025
$6.4M
NETWORK FUNCTION IN THE DEVELOPING SPINAL CORD OF THE CHICK EMBRYOZ01NS002787 · NINDS · NEUROLOGICAL DISORDERS AND STROKE · PI O'DONOVAN, MICHAEL J · 1990 to 2008
$2.2M
Development of synaptic inputs on spinal interneuronsR56NS047357 · NINDS · EMORY UNIVERSITY · PI ALVAREZ, FRANCISCO J · 2013 to 2013
$390k
Intramural NIH HHSNINDS NIH HHS NS047357NINDS NIH HHS R01 NS047357NINDS NIH HHS R56 NS047357
6 · The paper itself

Abstract

The mechanisms that diversify adult interneurons from a few pools of embryonic neurons are unknown. Renshaw cells, Ia inhibitory interneurons (IaINs), and possibly other types of mammalian spinal interneurons have common embryonic origins within the V1 group. However, in contrast to IaINs and other V1-derived interneurons, adult Renshaw cells receive motor axon synapses and lack proprioceptive inputs. Here, we investigated how this specific pattern of connectivity emerges during the development of Renshaw cells. Tract tracing and immunocytochemical markers [parvalbumin and vesicular glutamate transporter 1 (VGLUT1)] showed that most embryonic (embryonic day 18) Renshaw cells lack dorsal root inputs, but more than half received dorsal root synapses by postnatal day 0 (P0) and this input spread to all Renshaw cells by P10-P15. Electrophysiological recordings in neonates indicated that this input is functional and evokes Renshaw cell firing. VGLUT1-IR bouton density on Renshaw cells increased until P15 but thereafter decreased because of limited synapse proliferation coupled with the enlargement of Renshaw cell dendrites. In parallel, Renshaw cell postsynaptic densities apposed to VGLUT1-IR synapses became smaller in adult compared with P15. In contrast, vesicular acetylcholine transporter-IR motor axon synapses contact embryonic Renshaw cells and proliferate postnatally matching Renshaw cell growth. Like other V1 neurons, Renshaw cells are thus competent to receive sensory synapses. However, after P15, these sensory inputs appear deselected through arrested proliferation and synapse weakening. Thus, Renshaw cells shift from integrating sensory and motor inputs in neonates to predominantly motor inputs in adult. Similar synaptic weight shifts on interneurons may be involved in the maturation of motor reflexes and locomotor circuitry.

Indexed as

Afferent PathwaysAnimalsAnimals, NewbornCell DifferentiationInterneuronsIn Vitro TechniquesMiceMice, Inbred C57BLMotor NeuronsRatsRats, Sprague-DawleySpinal CordSynapses

Identifiers

PMID17182780
PMCPMC3008340
OpenAlexW2009132905

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.