Evidence map›Paper›PMID 35360491›Full record

ArticleFrontiers in cellular neuroscience2022

Pericyte Loss Leads to Capillary Stalling Through Increased Leukocyte-Endothelial Cell Interaction in the Brain.

Young-Geun Choe, Jin-Hui Yoon, Jongyoon Joo, Bokyung Kim, Seon Pyo Hong, Gou Young Koh, Dong-Seok Lee, Wang-Yuhl Oh, Yong Jeong

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. An integrated investigation of systemic and localized pathophysiological mechanisms of stroke and multimodal therapeutic strategies.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
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  15. Article
  16. Inhibiting CaNature neuroscience · 2024
    Article
  17. Article
  18. Pericytes in the disease spotlight.Trends in cell biology · 2024
    Review
  19. Review
  20. 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

9 authors at 4 institutions in 1 country.

Young-Geun ChoeDepartment of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.
Jin-Hui YoonCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Jongyoon JooKI for Health Science and Technology, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.
Bokyung KimSchool of Life Sciences and Biotechnology, College of Natural Sciences, Kyungpook National University, Daegu, South Korea.
Seon Pyo HongCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Gou Young KohCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Dong-Seok LeeSchool of Life Sciences and Biotechnology, College of Natural Sciences, Kyungpook National University, Daegu, South Korea.
Wang-Yuhl OhKI for Health Science and Technology, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.
Yong JeongDepartment of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.
Institute for Basic Science · KRKorea Advanced Institute of Science and Technology · KRKorea Institute of Brain Science · KRKyungpook National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The neurovascular unit is a functional unit composed of neurons, glial cells, pericytes, and endothelial cells which sustain brain activity. While pericyte is a key component of the neurovascular unit, its role in cerebral blood flow regulation remains elusive. Recently, capillary stalling, which means the transient interruption of microcirculation in capillaries, has been shown to have an outsized impact on microcirculatory changes in several neurological diseases. In this study, we investigated capillary stalling and its possible causes, such as the cerebral endothelial glycocalyx and leukocyte adhesion molecules after depleting pericytes postnatally in mice. Moreover, we investigated hypoxia and gliosis as consequences of capillary stalling. Although there were no differences in the capillary structure and RBC flow, longitudinal optical coherence tomography angiography showed an increased number of stalled segments in capillaries after pericyte loss. Furthermore, the extent of the cerebral endothelial glycocalyx was decreased with increased expression of leukocyte adhesion molecules, suggesting enhanced interaction between leukocytes and endothelial cells. Finally, pericyte loss induced cerebral hypoxia and gliosis. Cumulatively, the results suggest that pericyte loss induces capillary stalling through increased interaction between leukocytes and endothelial cells in the brain.

Indexed as

capillary stallingcerebral endothelial glycocalyxleukocyte adhesion moleculesleukocyte-endothelial cell interactionpericyte

Identifiers

PMID35360491
PMCPMC8962364
OpenAlexW4220857895

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.