Evidence map›Paper›PMID 35203385›Full record

ArticleCells2022

The Sonic Hedgehog Pathway Modulates Survival, Proliferation, and Differentiation of Neural Progenitor Cells under Inflammatory Stress In Vitro.

Mohamed Tail, Hao Zhang, Guoli Zheng, Maryam Hatami, Thomas Skutella, Andreas Unterberg, Klaus Zweckberger, Alexander Younsi

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  6. Review
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  8. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
  9. 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

8 authors at 1 institution in 1 country.

Mohamed TailDepartment of Neurosurgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Hao ZhangDepartment of Neurosurgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Guoli ZhengDepartment of Neurosurgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Maryam HatamiDepartment of Neuroanatomy, Institute for Anatomy and Cell Biology, University of Heidelberg, 69120 Heidelberg, Germany.
Thomas SkutellaDepartment of Neuroanatomy, Institute for Anatomy and Cell Biology, University of Heidelberg, 69120 Heidelberg, Germany.
Andreas UnterbergDepartment of Neurosurgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Klaus ZweckbergerDepartment of Neurosurgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Alexander YounsiDepartment of Neurosurgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-8218-9243
Heidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Sonic Hedgehog protein (Shh) has been extensively researched since its discovery in 1980. Its crucial role in early neurogenesis and endogenous stem cells of mature brains, as well as its recently described neuroprotective features, implicate further important effects on neuronal homeostasis. Here, we investigate its potential role in the survival, proliferation, and differentiation of neural precursors cells (NPCs) under inflammatory stress as a potential adjunct for NPC-transplantation strategies in spinal cord injury (SCI) treatment. To this end, we simulated an inflammatory environment in vitro using lipopolysaccharide (LPS) and induced the Shh-pathway using recombinant Shh or blocked it using Cyclopamine, a potent Smo inhibitor. We found that Shh mediates the proliferation and neuronal differentiation potential of NPCs in vitro, even in an inflammatory stress environment mimicking the subacute phase after SCI. At the same time, our results indicate that a reduction of the Shh-pathway activation by blockage with Cyclopamine is associated with reduced NPC-survival, reduced neuronal differentiation and increased astroglial differentiation. Shh might thus, play a role in endogenous NPC-mediated neuroregeneration or even be a potent conjunct to NPC-based therapies in the inflammatory environment after SCI.

Indexed as

Neural Stem CellsSpinal Cord InjuriesCell DifferentiationCell ProliferationHedgehog ProteinsHumansSignal TransductionHedgehog ProteinsCyclopaminedifferentiationin-vitroKi-67LPSneuroinflammationneuroregenerationNPCShhspinal cord injury

Identifiers

PMID35203385
PMCPMC8869809
OpenAlexW4212853609

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.