Evidence map›Paper›PMID 36380034›Full record

ArticleBrain structure & function2023

In mice and humans, brain microvascular contractility matures postnatally.

Leila Slaoui, Alice Gilbert, Armelle Rancillac, Barbara Delaunay-Piednoir, Audrey Chagnot, Quentin Gerard, Gaëlle Letort, Philippe Mailly, Noémie Robil, Antoinette Gelot and 10 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Brain structure & function, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Development of perivascular astrocyte processes.Frontiers in neuroscience · 2025
    Review
  5. Article
  6. Review
  7. 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

20 authors at 12 institutions in 1 country.

Leila Slaoui *Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL, Paris, France.
Alice Gilbert *Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL, Paris, France.
Armelle RancillacCenter for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL, Paris, France.
Barbara Delaunay-PiednoirCenter for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL, Paris, France.
Audrey ChagnotUNICAEN, INSERM UMR-S U1237, Physiopathology and Imaging of Neurological Disorders (PhIND), GIP Cyceron, Institute Blood and Brain @ Caen-Normandie (BB@C), Normandie University, 14000, Caen, France.
Quentin GerardUNICAEN, INSERM UMR-S U1237, Physiopathology and Imaging of Neurological Disorders (PhIND), GIP Cyceron, Institute Blood and Brain @ Caen-Normandie (BB@C), Normandie University, 14000, Caen, France.
Gaëlle LetortCenter for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL, Paris, France.
Philippe MaillyCenter for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL, Paris, France.
Noémie RobilGenosplice, Paris, France.
Antoinette GelotService d'anatomie et cytologie pathologie, Assistance Publique-Hôpitaux de Paris, Hôpital Armand Trousseau, Paris, France.
Mathilde LefebvreService de foetopathologie, Centre hospitalier régional d'Orleans, Orléans, France.
Maryline FavierHistIM Facility, Institut Cochin, Paris, France.
Karine DiasGenomiqueENS, Institut de Biologie de L'ENS (IBENS), Département de biologie, École normale supérieure, CNRS, INSERM, Université PSL, 75005, Paris, France.
Laurent JourdrenGenomiqueENS, Institut de Biologie de L'ENS (IBENS), Département de biologie, École normale supérieure, CNRS, INSERM, Université PSL, 75005, Paris, France.
Laetitia FedericiOptimisation Thérapeutique en Neuropsychopharmacologie, INSERM, Université de Paris, Paris, France.
Sylvain AuvityOptimisation Thérapeutique en Neuropsychopharmacologie, INSERM, Université de Paris, Paris, France.
Salvatore CisterninoOptimisation Thérapeutique en Neuropsychopharmacologie, INSERM, Université de Paris, Paris, France.
Denis VivienUNICAEN, INSERM UMR-S U1237, Physiopathology and Imaging of Neurological Disorders (PhIND), GIP Cyceron, Institute Blood and Brain @ Caen-Normandie (BB@C), Normandie University, 14000, Caen, France.
Martine Cohen-Salmon *Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL, Paris, France. martine.cohen-salmon@college-de-france.fr.
Anne-Cécile Boulay *Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL, Paris, France.
Centre Interdisciplinaire de Recherche en Biologie · FRCentre National de la Recherche Scientifique · FRInserm · FRCyceron · FRCentre hospitalier régional d'Orléans · FRÉcole Normale Supérieure - PSL · FRInstitut Cochin · FROptimisation Thérapeutique en NeuropsychopharmacologieSorbonne Université · FRUniversité de Caen Normandie · FRUniversité Paris Cité · FRUniversité Paris Sciences et Lettres · FR

Funding

Association Européenne contre les Leucodystrophies ELA2012-014C2BFondation Maladies Rares 20170603Fondation pour la Recherche Médicale AJE20171039094 and PLP20170939025p60Fondation pour la Recherche Médicale RAD22005DFA
6 · The paper itself

Abstract

Although great efforts to characterize the embryonic phase of brain microvascular system development have been made, its postnatal maturation has barely been described. Here, we compared the molecular and functional properties of brain vascular cells on postnatal day (P)5 vs. P15, via a transcriptomic analysis of purified mouse cortical microvessels (MVs) and the identification of vascular-cell-type-specific or -preferentially expressed transcripts. We found that endothelial cells (EC), vascular smooth muscle cells (VSMC) and fibroblasts (FB) follow specific molecular maturation programs over this time period. Focusing on VSMCs, we showed that the arteriolar VSMC network expands and becomes contractile resulting in a greater cerebral blood flow (CBF), with heterogenous developmental trajectories within cortical regions. Samples of the human brain cortex showed the same postnatal maturation process. Thus, the postnatal phase is a critical period during which arteriolar VSMC contractility required for vessel tone and brain perfusion is acquired and mature.

Indexed as

Endothelial CellsMuscle, Smooth, VascularAnimalsBrainHumansMiceMuscle ContractionBrain microvesselsCerebral blood flowMicrovessel contractilityPostnatal developmentVascular smooth muscle cell

Identifiers

PMID36380034
OpenAlexW4309103070

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.