Evidence map›Paper›PMID 31677479›Full record

ArticleiScience2019

Systematic Identification of Cell-Cell Communication Networks in the Developing Brain.

Bilal N Sheikh, Olga Bondareva, Sukanya Guhathakurta, Tsz Hong Tsang, Katarzyna Sikora, Nadim Aizarani, Sagar, Herbert Holz, Dominic Grün, Lutz Hein and 1 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 58 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Bilal N SheikhMax Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, Freiburg 79108, Germany. Electronic address: sheikh@ie-freiburg.mpg.de.
Olga BondarevaInstitute of Experimental and Clinical Pharmacology and Toxicology, University of Freiburg, Albertstr. 25, Freiburg 79104, Germany.
Sukanya GuhathakurtaMax Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, Freiburg 79108, Germany; Faculty of Biology, Albert Ludwig University of Freiburg, Freiburg 79104, Germany.
Tsz Hong TsangMax Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, Freiburg 79108, Germany; Faculty of Biology, Albert Ludwig University of Freiburg, Freiburg 79104, Germany.
Katarzyna SikoraMax Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, Freiburg 79108, Germany.
Nadim AizaraniMax Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, Freiburg 79108, Germany; Faculty of Biology, Albert Ludwig University of Freiburg, Freiburg 79104, Germany.
SagarMax Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, Freiburg 79108, Germany.
Herbert HolzMax Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, Freiburg 79108, Germany.
Dominic GrünMax Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, Freiburg 79108, Germany.
Lutz HeinInstitute of Experimental and Clinical Pharmacology and Toxicology, University of Freiburg, Albertstr. 25, Freiburg 79104, Germany.
Asifa AkhtarMax Planck Institute of Immunobiology and Epigenetics, Stuebeweg 51, Freiburg 79108, Germany. Electronic address: akhtar@ie-freiburg.mpg.de.
Max Planck Institute of Immunobiology and Epigenetics · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the generation of cell-type specific knockout models, the importance of inter-cellular communication between neural, vascular, and microglial cells during neural development has been increasingly appreciated. However, the extent of communication between these major cell populations remains to be systematically mapped. Here, we describe EMBRACE (embryonic brain cell extraction using FACS), a method to simultaneously isolate neural, mural, endothelial, and microglial cells to more than 94% purity in ∼4 h. Utilizing EMBRACE we isolate, transcriptionally analyze, and build a cell-cell communication map of the developing mouse brain. We identify 1,710 unique ligand-receptor interactions between neural, endothelial, mural, and microglial cells in silico and experimentally confirm the APOE-LDLR, APOE-LRP1, VTN-KDR, and LAMA4-ITGB1 interactions in the E14.5 brain. We provide our data via the searchable "Brain interactome explorer", available at https://mpi-ie.shinyapps.io/braininteractomeexplorer/. Together, this study provides a comprehensive map that reveals the richness of communication within the developing brain.

Indexed as

Developmental NeuroscienceNeuroscienceSystems NeuroscienceTechniques in Neuroscience

Identifiers

PMID31677479
PMCPMC6838536
OpenAlexW2981121538

What OpenQuestion 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 OpenQuestion graph.