Evidence map›Paper›PMID 29549645›Full record

ArticleMolecular neurobiology2019

Transplantation of Human Chorion-Derived Cholinergic Progenitor Cells: a Novel Treatment for Neurological Disorders.

Alireza Mohammadi, Ali Maleki-Jamshid, Davood Sanooghi, Peiman Brouki Milan, Arash Rahmani, Farshid Sefat, Koorosh Shahpasand, Mansoureh Soleimani, Mehrdad Bakhtiari, Rafie Belali and 4 more

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Article in Molecular neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Alireza MohammadiNeuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Ali Maleki-JamshidDepartment of Anatomy, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Davood SanooghiDepartment of Genetics, Faculty of Biological Sciences, Shahid Beheshti University, Tehran, Iran.
Peiman Brouki MilanCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Arash RahmaniCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Farshid SefatSchool of Engineering, Design and Technology-Medical Engineering, University of Bradford, Bradford, West Yorkshire, UK.
Koorosh ShahpasandDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Mansoureh SoleimaniDepartment of Anatomy, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mehrdad BakhtiariDepartment of Anatomy, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Rafie BelaliPhysiology Research Center and Department of Physiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Faezeh FaghihiCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran. faghihi.f@iums.ac.ir.
Mohammad Taghi JoghataeiDepartment of Anatomy, School of Medicine, Iran University of Medical Sciences, Tehran, Iran. mt.joghataei@yahoo.com.
George PerryNeurosciences Institute and Department of Biology, College of Sciences, University of Texas at San Antonio, San Antonio, TX, USA. george.perry@utsa.edu.
Masoud MozafariCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran. mozafari.masoud@gmail.com.ORCID http://orcid.org/0000-0002-0232-352X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A neurological disorder is any disorder or abnormality in the nervous system. Among different neurological disorders, Alzheimer's disease (AD) is recognized as the sixth leading cause of death globally. Considerable research has been conducted to find pioneer treatments for this devastating disorder among which cell therapy has attracted remarkable attentions over the last decade. Up to now, targeted differentiation into specific desirable cell types has remained a major obstacle to clinical application of cell therapy. Also, potential risks including uncontrolled growth of stem cells could be disastrous. In our novel protocol, we used basal forebrain cholinergic progenitor cells (BFCN) derived from human chorion-derived mesenchymal stem cells (hC-MSCs) which made it possible to obtain high-quality population of cholinergic neurons and in vivo in much shorter time period than previous established methods. Remarkably, the transplanted progenitors fully differentiated to cholinergic neurons which in turn integrated in higher cortical networks of host brains, resulting in significant improvement in cognitive assessments. This method may have profound implications in cell therapies for any other neurodegenerative disorders. Graphical Abstract ᅟ.

Indexed as

Stem Cell TransplantationAlzheimer DiseaseAnimalsCell DifferentiationCholinergic NeuronsChorionCognitionDisease Models, AnimalHumansMaleNervous System DiseasesProsencephalonRats, WistarRecovery of FunctionStem CellsAlzheimer’s diseaseBasal forebrain cholinergic progenitor cellsNeurological disorderStem cells

Identifiers

What Socratic 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 Socratic graph.