Evidence map›Paper›PMID 33904394›Full record

ArticleeLife2021

Vascular-derived SPARC and SerpinE1 regulate interneuron tangential migration and accelerate functional maturation of human stem cell-derived interneurons.

Matthieu Genestine, Daisy Ambriz, Gregg W Crabtree, Patrick Dummer, Anna Molotkova, Michael Quintero, Angeliki Mela, Saptarshi Biswas, Huijuan Feng, Chaolin Zhang and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. DurableMolecular therapy. Nucleic acids · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. hapln1aNature communications · 2023
    Article
  9. Review
  10. Article
  11. 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

15 authors at 2 institutions in 1 country.

Matthieu GenestineDepartment of Pathology and Cell Biology, Columbia University, New York, United States.
Daisy AmbrizDepartment of Pathology and Cell Biology, Columbia University, New York, United States.
Gregg W CrabtreeDepartment of Neurology, Columbia University Irving Medical Center, New York, United States.
Patrick DummerDepartment of Pathology and Cell Biology, Columbia University, New York, United States.
Anna MolotkovaDepartment of Pathology and Cell Biology, Columbia University, New York, United States.
Michael QuinteroDepartment of Pathology and Cell Biology, Columbia University, New York, United States.
Angeliki MelaDepartment of Pathology and Cell Biology, Columbia University, New York, United States.
Saptarshi BiswasDepartment of Neurology, Columbia University Irving Medical Center, New York, United States.
Huijuan FengDepartment of Department of Systems Biology, Columbia University Irving Medical Center, New York, United States.
Chaolin ZhangDepartment of Department of Systems Biology, Columbia University Irving Medical Center, New York, United States.ORCID 0000-0002-8310-7537
Peter CanollDepartment of Pathology and Cell Biology, Columbia University, New York, United States.
Gunnar HargusDepartment of Pathology and Cell Biology, Columbia University, New York, United States.
Dritan AgalliuDepartment of Pathology and Cell Biology, Columbia University, New York, United States.
Joseph A GogosDepartment of Cellular Physiology and Biophysics, Columbia University, New York, United States.
Edmund AuDepartment of Pathology and Cell Biology, Columbia University, New York, United States.ORCID 0000-0003-3190-9711
Columbia University · USColumbia University Irving Medical Center · US

Funding

RNA Regulatory Networks in Neuronal Cell Type Diversity and FunctionR01NS125018 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Chaolin Zhang · 2022 to 2026
$3.0M
Cellular and humoral immune mechanisms underlying neurovascular dysfunction in autoimmune encephalitisR01MH112849 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI AGALLIU, DRITAN, CUTFORTH, TYLER · 2017 to 2020
$2.1M
Studying the Molecular Regulation of MGE Projection Neuron Identity by St18R01NS117695 · NINDS · WINIFRED MASTERSON BURKE MED RES INST · PI AU, EDMUND · 2021 to 2025
$2.0M
Single-nucleotide resolution mapping of allelic protein-RNA interactions and splicing-regulatory variantsR01GM124486 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ZHANG, CHAOLIN · 2018 to 2021
$1.8M
RNA regulatory networks in motor neuron development and functionR01NS089676 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ZHANG, CHAOLIN · 2015 to 2019
$1.8M
Developing a microfluidic human neurovascular unit system to investigate genetic and age-related risk factors in Alzheimer's diseaseR01AG078352 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Dritan Agalliu, Andrew Alexander Sproul · 2025 to 2026
$837k
The role of autophagy in the neurovascular unit for the physiological response to stress.R21NS118891 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI AGALLIU, DRITAN, YAMAMOTO, AI · 2020 to 2020
$438k
Developing a stem cell-based model to study MGE and CGE interneuron lineage specificationR03MH119443 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI AU, EDMUND · 2019 to 2020
$162k
NIA NIH HHS R01 AG078352NIMH NIH HHS R01 MH112849NIMH NIH HHS R03 MH119443NINDS NIH HHS R01 NS089676NINDS NIH HHS R01 NS117695NINDS NIH HHS R01 NS125018NINDS NIH HHS R21 NS118891
6 · The paper itself

Abstract

Cortical interneurons establish inhibitory microcircuits throughout the neocortex and their dysfunction has been implicated in epilepsy and neuropsychiatric diseases. Developmentally, interneurons migrate from a distal progenitor domain in order to populate the neocortex - a process that occurs at a slower rate in humans than in mice. In this study, we sought to identify factors that regulate the rate of interneuron maturation across the two species. Using embryonic mouse development as a model system, we found that the process of initiating interneuron migration is regulated by blood vessels of the medial ganglionic eminence (MGE), an interneuron progenitor domain. We identified two endothelial cell-derived paracrine factors, SPARC and SerpinE1, that enhance interneuron migration in mouse MGE explants and organotypic cultures. Moreover, pre-treatment of human stem cell-derived interneurons (hSC-interneurons) with SPARC and SerpinE1 prior to transplantation into neonatal mouse cortex enhanced their migration and morphological elaboration in the host cortex. Further, SPARC and SerpinE1-treated hSC-interneurons also exhibited more mature electrophysiological characteristics compared to controls. Overall, our studies suggest a critical role for CNS vasculature in regulating interneuron developmental maturation in both mice and humans.

Indexed as

Action PotentialsAnimalsCell MovementCerebral CortexEndothelial CellsHEK293 CellsHumansInduced Pluripotent Stem CellsInterneuronsIntracellular Signaling Peptides and ProteinsMedian EminenceMembrane ProteinsMiceMice, 129 StrainMice, Inbred C57BLMice, Inbred NODApcdd1 protein, mouseIntracellular Signaling Peptides and ProteinsMembrane ProteinsOsteonectinPlasminogen Activator Inhibitor 1brain developmentdevelopmental biologyhumaninterneuronmouseneovascularizationneuroscience

Identifiers

PMID33904394
PMCPMC8099424
OpenAlexW3157432718

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.